Product Details

SNP ID

rs610142

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15678120 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTATTTCCATCCTGTTTACCTTCA[A/T]ATGCTAATCTCTTCTCAAACACCCT

Phenotype

MIM: 611485

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CYP4F12 PubMed Links

Gene Details

Gene

CYP4F12

Gene Name

cytochrome P450 family 4 subfamily F member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023944.3		Intron			NP_076433.3
XM_006722850.3		Intron			XP_006722913.1
XM_011528202.2		Intron			XP_011526504.1
XM_011528203.2		Intron			XP_011526505.1
XM_011528204.2		Intron			XP_011526506.1
XM_011528205.2		Intron			XP_011526507.1
XM_011528207.2		Intron			XP_011526509.1
XM_011528208.2		Intron			XP_011526510.1
XM_017027172.1		Intron			XP_016882661.1

View Full Product Details