S27R (p.Ser27Arg) variant of CDKN1A (P38936)
S27R (p.Ser27Arg) in CDKN1A (P38936) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes population frequency data and structural context.
S27R (p.Ser27Arg) variant details
- p.Ser27Arg
- ExAC rs762818650
- TOPMed rs762818650
- gnomAD rs762818650
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Population evidence available
- Structural context available