Product Details

SNP ID
rs147318633
Assay Type
Functionally Tested
NCBI dbSNP Submissions
13
Location
Chr.1:247896011 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGATCATGAACCCCAGGCTCTGCC[A/G]GGGCTTGGTGTCAGTGACCTGGGGC
Phenotype
MIM: 616729
Polymorphism
A/G, 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_001001957.2 425 Missense Mutation CAG,CGG Q142R NP_001001957.2

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