Product Details

SNP ID

rs11572178

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:95037335 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAAGATAACAAAGAAAGGAAGTA[A/G]TTACTCCTTGTGTTTAACTGTGACT

Phenotype

MIM: 601129

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CYP2C8 PubMed Links

Gene Details

Gene

CYP2C8

Gene Name

cytochrome P450 family 2 subfamily C member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000770.3		Intron			NP_000761.3
NM_001198853.1		Intron			NP_001185782.1
NM_001198854.1		Intron			NP_001185783.1
NM_001198855.1		Intron			NP_001185784.1

View Full Product Details