Product Details

SNP ID
rs765598920
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:99758182 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTGACTCAACCTTTAGAACAACG[G/T]GTTTTTCTGGTTGAAGAAGTCCTCC
Phenotype
MIM: 124010
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CYP3A4 PubMed Links

Gene Details

Gene
CYP3A4
Gene Name
cytochrome P450 family 3 subfamily A member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202855.2 1567 Missense Mutation CAC,CCC H487P NP_001189784.1
NM_017460.5 1567 Missense Mutation CAC,CCC H488P NP_059488.2
XM_017011780.1 1567 Intron XP_016867269.1

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