A41V (p.Ala41Val) variant of CDC42 (P60953)
A41V (p.Ala41Val) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data, published literature, and structural context.
A41V (p.Ala41Val) variant details
- p.Ala41Val
- gnomAD 1-22081738-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.747
- CADD 24.90
- PolyPhen-2 0.17
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available