Product Details

SNP ID: rs200017985
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:98087671 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTGGTTCATGTGAGTTTACTATTG[C/T]GACTAACTTTCTGCAGGTTTAACAT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: OR5AC2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_054106.1	499	Nonsense Mutation	CGA,TGA	R167*	NP_473447.1