Product Details

SNP ID

rs499033

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:59713478 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGAGGGTGACAGATCGCTATAAAC[C/T]GGTCATAAGCCATGACTACCAGCAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

OR10V1 PubMed Links

Additional Information

For this assay, SNP(s) [rs499037] are located under a probe 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

OR10V1

Gene Name

olfactory receptor family 10 subfamily V member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005324.1	368	Missense Mutation			NP_001005324.1

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