Product Details

SNP ID: rs139856982
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:55967758 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCAAAGAATAAGATTACAACTATTA[A/G]GTGAGATGAGCAGGTGGAGAAGGCT
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	706	Silent Mutation	CTA,TTA	L236L	NP_001005491.1