Product Details

SNP ID: rs138179143
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:21155011 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCTTGTTTCTCAAAGAGTACATGA[A/G]GGGGTTCAGCACTGGGATCACCACT
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	1015	Missense Mutation	ATC,GTC	I339V	NP_001004731.1