S27G (p.Ser27Gly) variant of CDKN1A (P38936)
S27G (p.Ser27Gly) in CDKN1A (P38936) is a missense change. The record also includes population frequency data and structural context.
S27G (p.Ser27Gly) variant details
- p.Ser27Gly
- ExAC rs775222810
- TOPMed rs775222810
- gnomAD rs775222810
- Missense
- Population evidence available
- Structural context available