Product Details

SNP ID: rs145233416
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:148827096 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTCATGGGCCTGGCAGTGGTGCCC[C/T]TTGGGGCCGCCCATATTCTTATGAA
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	504	Missense Mutation	CTT,TTT	L89F	NP_000015.1