Product Details

SNP ID

rs189993261

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:247896010 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGATCATGAACCCCAGGCTCTGC[C/T]GGGGCTTGGTGTCAGTGACCTGGGG

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	424	Missense Mutation	CGG,TGG	R142W	NP_001001957.2

View Full Product Details