Product Details

SNP ID

rs16980628

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15615534 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATCTCCCTCCATGCTCTTAACCAT[G/T]TTTACCCATCATTGGTCCTGGAGCT

Phenotype

MIM: 611545

Polymorphism

G/T, 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		Intron			NP_009184.1
XM_017026232.1		Intron			XP_016881721.1

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