V14F (p.Val14Phe) variant of CDC42 (P60953)
V14F (p.Val14Phe) 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.
V14F (p.Val14Phe) variant details
- p.Val14Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.86
- MetaSVM 1.04
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available