Product Details

SNP ID: rs202043963
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:56030669 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCAATCACTCCTAAAATGCTGGCAA[A/G]CTTCTTGGCATCCAGGAAAAGCATC
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR5AS1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001921.1	251	Missense Mutation	AAC,AGC	N84S	NP_001001921.1