Product Details

SNP ID

rs142090161

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:104569441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCTTTCTGGCAGTAAAGAAAAAG[C/G]TTTCCTTCTCTGGGTGTATGGTGCA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OR13C8 PubMed Links

Gene Details

Gene

OR13C8

Gene Name

olfactory receptor family 13 subfamily C member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004483.1	274	Missense Mutation	CTT,GTT	L92V	NP_001004483.1

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