D33H (p.Asp33His) variant of CDKN1A (P38936)
D33H (p.Asp33His) in CDKN1A (P38936) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes population frequency data and structural context.
D33H (p.Asp33His) variant details
- p.Asp33His
- ESP rs376481017
- ExAC rs376481017
- TOPMed rs376481017
- gnomAD rs376481017
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available