Product Details

SNP ID: rs61742762
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:56641563 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTATTTTTTAAACTATAGATGAGGG[G/T]ATTTAGCACAGGGATTATTACTGTA
Phenotype
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: OR5AP2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002925.1	877	Missense Mutation	ACC,CCC	T293P	NP_001002925.1