Product Details

SNP ID

rs201456288

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15615735 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCGCATCCTGGCCTGGACCTATG[A/C]CTTCTATCACAACGGCCGCCGCCTC

Phenotype

MIM: 611545

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CYP4F8 PubMed Links

Gene Details

Gene

CYP4F8

Gene Name

cytochrome P450 family 4 subfamily F member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007253.3	120	Missense Mutation	GAC,GCC	D40A	NP_009184.1
XM_017026232.1	120	Missense Mutation	GAC,GCC	D40A	XP_016881721.1

View Full Product Details