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SNP ID

rs200933239

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:248180004 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCATCATGGCATGGGAGAATCAG[A/G]CCTTCAACTCCGACTTCATCCTCCT

Phenotype

Polymorphism

A/G, Transition 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	19	Missense Mutation	ACC,GCC	T7A	NP_001004688.1

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