Product Details

SNP ID: rs145643593
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:21155007 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACATCCTTGTTTCTCAAAGAGTAC[A/G]TGAGGGGGTTCAGCACTGGGATCAC
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	1019	Missense Mutation	ACG,ATG	T340M	NP_001004731.1