Product Details

SNP ID

rs12564525

Assay Type

DME

NCBI dbSNP Submissions

44

Location

Chr.1:47141609 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

TGGATCCTACAAATTCCTGGCTCCA[C/T]GGATTGGTATGTGTGCAAACTAGGA

Phenotype

MIM: 615341

Polymorphism

C/T, Transition substitution

Allele Nomenclature

CYP4A22*11,c.376C>T CYP4A22*11,g.4124C>T CYP4A22*12A,c.376C>T CYP4A22*12A,g.4124C>T CYP4A22*12B,c.376C>T CYP4A22*12B,g.4124C>T CYP4A22*13A,c.376C>T CYP4A22*13A,g.4124C>T CYP4A22*13B,c.376C>T CYP4A22*13B,g.4124C>T CYP4A22*14,c.376C>T CYP4A22*14,g.4124C>T CYP4A22*15,c.376C>T CYP4A22*15,g.4124C>T CYP4A22*8,c.376C>T CYP4A22*8,g.4124C>T CYP4A22*9,c.376C>T CYP4A22*9,g.4124C>T

Literature Links

CYP4A22 PubMed Links

Gene Details

Gene

CYP4A22

Gene Name

cytochrome P450 family 4 subfamily A member 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010969.3		Intron			NP_001010969.2
NM_001308102.1		Intron			NP_001295031.1
XM_005270767.3		Intron			XP_005270824.1
XM_005270770.3		Intron			XP_005270827.1

View Full Product Details