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SNP ID

rs201832076

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:248180029 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTTCAACTCCGACTTCATCCTCC[C/T]TGGAATCTTCAATCACAGCCCACCA

Phenotype

Polymorphism

C/T, 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	44	Missense Mutation	CCT,CTT	P15L	NP_001004688.1

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