C13G (p.Cys13Gly) variant of CDKN1A (P38936)
C13G (p.Cys13Gly) in CDKN1A (P38936) is a missense change. The record also includes population frequency data.
C13G (p.Cys13Gly) variant details
- p.Cys13Gly
- 1000Genomes rs199896504
- ExAC rs199896504
- TOPMed rs199896504
- gnomAD rs199896504
- Missense
- Population evidence available