Product Details

SNP ID
rs1058932
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.10:95037104 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
AAAGAGTTGCAGGTGATAGCAGATC[A/G]GCAGCCAGATGGGCTAGCATTCTTC
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 1592 UTR 3 NP_000761.3
NM_001198853.1 1592 UTR 3 NP_001185782.1
NM_001198854.1 1592 UTR 3 NP_001185783.1
NM_001198855.1 1592 UTR 3 NP_001185784.1

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