Product Details

SNP ID: rs3820678
Assay Type: Functionally tested
NCBI dbSNP Submissions: 83
Location: Chr.1:158480448 on Build GRCh38
Set Membership: HapMap JSNP
Context Sequence [VIC/FAM]: AGTTTTCAGCCTCCCTTTTTGTAGC[A/G]CCAACAAAGTCAATCATTACTTCTG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR10R2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004472.1	571	Missense Mutation	ACC,GCC	T191A	NP_001004472.1