Product Details

SNP ID: rs61896165
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:55968042 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCAATTACTACAGGAATTGTGATG[A/G]TCCAGGAAGCTATTATCAGCTGAAT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR10AG1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005491.1	422	Missense Mutation	ACC,ATC	T141I	NP_001005491.1