D76G (p.Asp76Gly) variant of CDC42 (P60953)
D76G (p.Asp76Gly) in CDC42 (P60953) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
D76G (p.Asp76Gly) variant details
- p.Asp76Gly
- TOPMed rs1645663483
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available