Product Details

SNP ID: rs200759945
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:59365224 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCTGTTTCCCTCTTCTATACATCA[A/G]GAATCTTTGTCTATTTGAGTTCCAG
Phenotype: MIM: 615702
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR5AN1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004729.1	766	Missense Mutation	AGA,GGA	R256G	NP_001004729.1