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SNP ID

rs139324473

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:247895873 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGACAAGACCATCAGCTACATGG[A/G]CTGTGCCATCCAGCTCTTCCTGTTC

Phenotype

MIM: 616729

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

OR2W3 PubMed Links

Gene Details

Gene

OR2W3

Gene Name

olfactory receptor family 2 subfamily W member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001957.2	287	Missense Mutation	GAC,GGC	D96G	NP_001001957.2

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