Product Details

SNP ID: rs140685961
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:148826858 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGGCAACCCGGGAACGGCAGCGC[C/T]TTCTTGCTGGCACCCAATGGAAGCC
Phenotype: MIM: 109690
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ADRB2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000024.5	266	Silent Mutation	GCC,GCT	A9A	NP_000015.1