A13P (p.Ala13Pro) variant of CDC42 (P60953)
A13P (p.Ala13Pro) 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.
A13P (p.Ala13Pro) variant details
- p.Ala13Pro
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10021
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available