Product Details

SNP ID

rs17882687

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.10:94762760 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

TCTCTCATGTTTGCTTCTCCTTTCA[A/C]TCTGGAGACAGAGCTCTGGGAGAGG

Phenotype

MIM: 124020

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

CYP2C19*15,c.55A>C CYP2C19*15,g.55A>C

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	80	Missense Mutation	ATC,CTC	I19L	NP_000760.1

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