R32H (p.Arg32His) variant of CDKN1A (P38936)
R32H (p.Arg32His) in CDKN1A (P38936) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The record also includes population frequency data and structural context.
R32H (p.Arg32His) variant details
- p.Arg32His
- NCI-TCGA Cosmic COSV5519
- cosmic curated COSV55191
- TOPMed rs1477458254
- gnomAD rs1477458254
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Population evidence available
- Structural context available