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SNP ID

rs144483053

Assay Type

Functionally tested

NCBI dbSNP Submissions

15

Location

Chr.1:248180933 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAAGTCTGAGAGTGAGTTACCTCA[A/T]AAACTTTATGTTTTGCTGTTTGCTA

Phenotype

Polymorphism

A/T, 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	948	Missense Mutation	CAA,CAT	Q316H	NP_001004688.1

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