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SNP ID

rs62639688

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:55913673 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTAAAATAAAATTTTATTTTTCA[C/G]TTTTTTCAGGGCCTCTTTCACATCC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OR5W2 PubMed Links

Gene Details

Gene

OR5W2

Gene Name

olfactory receptor family 5 subfamily W member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001960.1	910	Missense Mutation	CTG,GTG	L304V	NP_001001960.1

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