Product Details

SNP ID

rs2072269

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15913929 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGTTTCTGGGGGCAAAAGTGAGGG[A/G]ATCTGACTGTGCCCATGACCCCCAT

Phenotype

MIM: 611517

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CYP4F11 PubMed Links

Gene Details

Gene

CYP4F11

Gene Name

cytochrome P450 family 4 subfamily F member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128932.1		Intron			NP_001122404.1
NM_021187.3		Intron			NP_067010.3

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