Product Details

SNP ID

rs148268889

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:247895686 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCCTCTTTGTGGTCATCCTGATC[A/G]CGTACCTCCTGACCCTCGTAGGCAA

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	100	Missense Mutation	ACG,GCG	T34A	NP_001001957.2

View Full Product Details