Product Details

SNP ID

rs200867914

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:247895644 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCATCCTACTGGGATTCTCTGAC[C/T]GACCCCATCTGGAGAGGATCCTCTT

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	58	Nonsense Mutation	CGA,TGA	R20*	NP_001001957.2

View Full Product Details