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SNP ID

rs146796261

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:248180059 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTTCAATCACAGCCCACCACACA[A/C]GTTCCTCTTCTTTCTGGTCCTGGGC

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

OR2M2 PubMed Links

Gene Details

Gene

OR2M2

Gene Name

olfactory receptor family 2 subfamily M member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004688.1	74	Missense Mutation	AAG,ACG	K25T	NP_001004688.1

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