Product Details

SNP ID: rs201657808
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:48202736 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGAGGGTCCCCACAAGAGAGGCCA[A/G]TCACTATGGGGGCCTCACAGAAGAA
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR10AD1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004134.1	557	Missense Mutation	ACT,ATT	T186I	NP_001004134.1