Product Details

SNP ID: rs4996
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:37965342 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAACGCCCGAGGGGAAGAGGGCCGG[G/A]CGGGCGGCGGCGCAGGGCTCCGGAG
Phenotype: MIM: 109691
Polymorphism: G/A, Transition substitution
Allele Nomenclature
Literature Links: ADRB3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000025.2	1325	Silent Mutation			NP_000016.1