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SNP ID: rs2687076
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:99709645 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAGAGGTTACACGTCTGTAACCAAG[A/G]AAGTGAAAACAGATAGAAAAAGCAA
Phenotype: MIM: 605340
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CYP3A7 PubMed Links

Gene Details

Gene: CYP3A7
Gene Name: cytochrome P450 family 3 subfamily A member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000765.4		Intron			NP_000756.3

Gene: CYP3A7-CYP3A51P
Gene Name: CYP3A7-CYP3A51P readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256497.2		Intron			NP_001243426.2

Gene: ZSCAN25
Gene Name: zinc finger and SCAN domain containing 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145115.2		Intron			NP_660090.2
XM_005250194.2		Intron			XP_005250251.1
XM_011515905.2		Intron			XP_011514207.1
XM_011515906.2		Intron			XP_011514208.1
XM_011515907.2		Intron			XP_011514209.1
XM_011515908.2		Intron			XP_011514210.1
XM_011515909.2		Intron			XP_011514211.1
XM_011515910.2		Intron			XP_011514212.1
XM_017011824.1		Intron			XP_016867313.1
XM_017011825.1		Intron			XP_016867314.1
XM_017011826.1		Intron			XP_016867315.1
XM_017011827.1		Intron			XP_016867316.1

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