Product Details

SNP ID
rs2901783
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:94693342 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTCCCACCTCCCTTTTTTGCTTTG[A/G]CTTTTGCCATGTGAGTGAAAGCTCC
Phenotype
MIM: 601131
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CYP2C18 PubMed Links

Gene Details

Gene
CYP2C18
Gene Name
cytochrome P450 family 2 subfamily C member 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000772.2 Intron NP_000763.1
NM_001128925.1 Intron NP_001122397.1

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