C17W (p.Cys17Trp) variant of PIK3CG (P48736)
C17W (p.Cys17Trp) in PIK3CG (P48736) is a missense change. The record also includes structural context.
C17W (p.Cys17Trp) variant details
- p.Cys17Trp
- 1000Genomes rs3729673
- ESP rs3729673
- ExAC rs3729673
- TOPMed rs3729673
- Missense
- Structural context available