A41T (p.Ala41Thr) variant of CDC42 (P60953)
A41T (p.Ala41Thr) in CDC42 (P60953) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
A41T (p.Ala41Thr) variant details
- p.Ala41Thr
- NCI-TCGA Cosmic COSV5966
- cosmic curated COSV59662
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.35
- MetaSVM -0.18
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available