Product Details

SNP ID: rs150928239
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:56030721 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCCTTATGGGTGTGCACTACAAAT[A/G]TTTTTCTTCGCTTCTTTTGCTGATG
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	303	Missense Mutation	ATA,ATG	I101M	NP_001001921.1