Product Details

SNP ID

rs609290

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:15678330 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

GGCCACCTATTCCCAGGGCTTTACG[A/G]TATGGCTGGGTCCCATCATCCCCTT

Phenotype

MIM: 611485

Polymorphism

A/G, Transition 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	329	Intron			NP_076433.3
XM_006722850.3	329	Intron			XP_006722913.1
XM_011528202.2	329	Intron			XP_011526504.1
XM_011528203.2	329	Intron			XP_011526505.1
XM_011528204.2	329	Intron			XP_011526506.1
XM_011528205.2	329	Intron			XP_011526507.1
XM_011528207.2	329	Intron			XP_011526509.1
XM_011528208.2	329	Intron			XP_011526510.1
XM_017027172.1	329	Missense Mutation	ATA,GTA	I90V	XP_016882661.1

View Full Product Details