Product Details

SNP ID

rs6583954

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:94774506 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGTGGAGACTATTGGCCCAGCAAT[C/T]GGGACCTCTACATGGGCTTTTGGGA

Phenotype

MIM: 124020

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CYP2C19 PubMed Links

Additional Information

For this assay, SNP(s) [rs17885348] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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		Intron			NP_000760.1

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