Product Details

SNP ID: rs61896164
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:55967804 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGGCTTTAGCCTTTCCTCTGGCTGA[A/T]GACAATTTCAAAATGTTGGAGATAA
Phenotype
Polymorphism: A/T, Transversion 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	660	Silent Mutation	TCA,TCT	S220S	NP_001005491.1