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SNP ID

rs137925587

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:248239277 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAGCTGAATGTTTCTTGTTGGCT[C/G]TCATGGCTTATGACCGCTATGTGGC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OR2M4 PubMed Links

Gene Details

Gene

OR2M4

Gene Name

olfactory receptor family 2 subfamily M member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017504.1	349	Missense Mutation	CTC,GTC	L117V	NP_059974.1

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