Product Details

SNP ID: rs149072229
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:94775130 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACGCATGGTGGTGCTGCATGGATAT[A/G]AAGTGGTGAAGGAAGCCCTGATTGA
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	266	Missense Mutation	AAA,GAA	K81E	NP_000760.1