Product Details

SNP ID: rs149446306
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:59365122 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTTATCATGATATCCTATGGCTAT[A/G]TTGGCATCTCCATCATGAAGATCAC
Phenotype: MIM: 615702
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR5AN1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004729.1	664	Missense Mutation	ATT,GTT	I222V	NP_001004729.1