vocab
allele
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
carrier
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
chromatin
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
chromosome
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
codon
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
diploid
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
dominant allele
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
enhancer
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
exon
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
gene
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
gene flow
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
genome
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
GWAS
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
genotype
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
germline cells
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
haploid
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
haplotype
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
heterozygous
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
homozygous
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
incomplete penetrance
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
indel
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
intron
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
karyotype
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
missense mutation
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
monogenic trait
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
multigenic trait
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
mutation
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
nonsense mutation
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
pharmacodynamics
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
pharmacogenetics
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
pharmacogenomics
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
pharmacokinetics
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
phenotype
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
polymorphism
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
recessive allele
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
recombination
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
reference sequenced number
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
sex linked trait
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
suppressor
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
transcription
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
transcription factors
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
SNP
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
translation
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
transposons
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
wild type
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
cells contain two copies of a gene
the relationship of time and drug absorption, distribution, metabolism and excretion
region of DNA that contains instructions to make proteins
the transfer of alleles from one population to another
the series of polymorphisms that are inherited together
change of an AA specifying codon to a stop codon
cells that contain 1 copy of the gene
possessing two of the same alleles for the same trait
insertion or deletion of DNA either as single nucleotide or spanning regions of DNA involving many nucleotides
a series of three adjacent bases in one polynucleotide chain of a DNA or RNA molecule, which codes for a specific amino acid
the entire DNA of the organism
proteins that bind to specific DNA sequences and modify rates of transcription
a unique identifier of a given SNP
the cells involved in reproduction
any heritable genetic change
• A portion of DNA that codes for a section of the mature messenger RNA obtained from that DNA, and is therefore expressed ("translated" into protein) at the ribosome
a mutation in DNA in a given population that may be observed at great than 1% frequency
massive screen of genomes of different populations to look for common connections between variations and disease
only one copy is necessary to see the trait
characteristic derived from a single gene
DNA sequences that move from one location in the genome to another
a profile (number and appearance) of an organism's chromosomes
results in the substitution of one AA for another
a long, single piece of DNA with multiple genes
characteristic derived from multiple genes
an individual who has a recessive allele but does not display the trait
the specific set of alleles inherited at a locus on a given gene
the relationship between drug exposure and pharmacologic response
the study of a gene involved in response to a drug
the study of many genes involved in response to a drug
DNA sequence that promotes transcription of a gene
expression of a physical trait or function due to genetic makeup or other factors
possessing two different alleles for the same trait
requires the presence of both alleles to see the trait
the exchange of genetic infomation during meiosis that leads to the production of a new set of alleles
nucleotide sequence in DNA that does not code infomation for protein synthesis and is removed before translation of mRNA
trait of gene located on X and Y chromosomes
a mutation that alleviates or reverts the phenotype of the original mutation
the process of reading DNA and making a complementary RNA copy
when a trait does not affect 100% of the people with that genotype
a variant DNA sequence in which a single nucleotide has been replaced by another base
the process of reading RNA and making proteins
the typical or normally occuring genotype of an organism
one of two or more forms of a gene
DNA and associated proteins in a genome
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