Product Details

SNP ID: rs4998
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.8:37963968 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: AAAGCCAGCCTGCTGCTCCACGGCA[C/G]CTGGACACTACCACTGAGGGAGGAG
Phenotype: MIM: 109691
Polymorphism: C/G, Transversion 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	1674	UTR 3			NP_000016.1