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SNP ID

rs61748963

Assay Type

Functionally tested

NCBI dbSNP Submissions

37

Location

Chr.1:247605760 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGGATCCCCCTCTTCATACCCCA[A/G]TGTACTTTTTTCTCAGCAACCTCTC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

OR2G3 PubMed Links

Gene Details

Gene

OR2G3

Gene Name

olfactory receptor family 2 subfamily G member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001914.1	175	Missense Mutation	ATG,GTG	M59V	NP_001001914.1

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