Product Details

SNP ID: rs199718040
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:59364687 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTCATAGATGTCTGCTATATCAGC[C/T]CCACAGTCCCCAAGATGCTCTCCAA
Phenotype: MIM: 615702
Polymorphism: C/T, 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	229	Missense Mutation	CCC,TCC	P77S	NP_001004729.1