Product Details

SNP ID: rs149199162
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:148827213 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGCATTGAGACCCTGTGCGTGATC[G/T]CAGTGGATCGCTACTTTGCCATTAC
Phenotype: MIM: 109690
Polymorphism: G/T, Transversion 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	621	Missense Mutation	GCA,TCA	A128S	NP_000015.1