R19M (p.Arg19Met) variant of PIK3CG (P48736)
R19M (p.Arg19Met) in PIK3CG (P48736) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R19M (p.Arg19Met) variant details
- p.Arg19Met
- ExAC rs767132637
- TOPMed rs767132637
- gnomAD rs767132637
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available