Product Details

SNP ID: rs141745866
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:59364718 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCCCCAAGATGCTCTCCAACCTCT[G/T]ACAGGAACAGCAAACTATCACTTTT
Phenotype: MIM: 615702
Polymorphism: G/T, Transversion 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	260	Nonsense Mutation	TGA,TTA	*87L	NP_001004729.1