Product Details

SNP ID: rs2234235
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:9629183 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGGAACTTTTTTGCATTTTGTTTCA[A/G]TTTAGGATTTCCTAAAATTAAGATG
Phenotype: MIM: 604796
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TAS2R1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019599.2	1169	Silent Mutation	CTG,TTG	L284L	NP_062545.1