Product Details

SNP ID: rs150718773
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:21155207 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCGAGCTCATTTTCAGGATGGTGTT[A/G]AGAATTAAGAAGTAGGAGATCAAGA
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR5AU1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004731.1	819	Silent Mutation	CTC,CTT	L273L	NP_001004731.1