Product Details

SNP ID: rs140420820
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:148827076 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCACTGGCCTGTGCTGATCTGGTCA[A/T]GGGCCTGGCAGTGGTGCCCTTTGGG
Phenotype: MIM: 109690
Polymorphism: A/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	484	Missense Mutation	AAG,ATG	K82M	NP_000015.1