Product Details

SNP ID

rs145328984

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:94775106 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCACTCTGTATTTTGGCCTGGAA[C/T]GCATGGTGGTGCTGCATGGATATGA

Phenotype

MIM: 124020

Polymorphism

C/T, 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	242	Missense Mutation	CGC,TGC	R73C	NP_000760.1

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