Product Details

SNP ID: rs75457182
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:59364943 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCACTGCTTCTTTATTCCAAATTG[C/G]TGCTTTGCTTCAACTCCACTTCTGT
Phenotype: MIM: 615702
Polymorphism: C/G, Transversion 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	485	Missense Mutation	GCT,GGT	A162G	NP_001004729.1