Product Details

SNP ID
rs151106761
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:94688216 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTTGGGATGGGGAAGAGGAGCAT[C/T]GAGGACCGTGTTCAAGAGGAAGCCC
Phenotype
MIM: 601131
Polymorphism
C/T, 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_000772.2 749 Silent Mutation ATC,ATT I141I NP_000763.1
NM_001128925.1 749 Silent Mutation ATC,ATT I141I NP_001122397.1

View Full Product Details