Product Details

SNP ID
rs57700608
Assay Type
DME
NCBI dbSNP Submissions
NA
Location
Chr.10:94780544 on Build GRCh38
Set Membership
DME Validated Inventoried
Context Sequence [VIC/FAM]
TTCATCCTGGGCTGTGCTCCCTGCA[A/G]TGTGATCTGCTCCATTATTTTCCAG
Phenotype
MIM: 124020
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CYP2C19 PubMed Links

Gene Details

Gene
CYP2C19
Gene Name
cytochrome P450 family 2 subfamily C member 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000769.2 552 Missense Mutation AAT,AGT N176S NP_000760.1

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