Product Details

SNP ID

rs202185882

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:247895750 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGTGTCCCGGCTGGACCCCCACC[C/T]CCACACCCCCATGTACTTCTTCCTC

Phenotype

MIM: 616729

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR2W3 PubMed Links

Gene Details

Gene

OR2W3

Gene Name

olfactory receptor family 2 subfamily W member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001957.2	164	Missense Mutation	CCC,CTC	P55L	NP_001001957.2

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