E62D (p.Glu62Asp) variant of CDC42 (P60953)
E62D (p.Glu62Asp) in CDC42 (P60953) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E62D (p.Glu62Asp) variant details
- p.Glu62Asp
- NCI-TCGA Cosmic COSV5966
- cosmic curated COSV59661
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available