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

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