A182S (p.Ala182Ser) variant of BIN1 (O00499)
A182S (p.Ala182Ser) in BIN1 (O00499) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A182S (p.Ala182Ser) variant details
- p.Ala182Ser
- ExAC rs779607755
- TOPMed rs779607755
- gnomAD rs779607755
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available