R66K (p.Arg66Lys) variant of CDC42 (P60953)
R66K (p.Arg66Lys) 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.
R66K (p.Arg66Lys) variant details
- p.Arg66Lys
- NCI-TCGA Cosmic COSV5966
- cosmic curated COSV59662
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available