Product Details

SNP ID: rs112851828
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:98087399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTAGCCTTTTCAGATGCTTGTACTT[A/C]AACCTCTATAACCCCTAGGATGCTG
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: OR5AC2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_054106.1	227	Nonsense Mutation	TAA,TCA	*76S	NP_473447.1