L20V (p.Leu20Val) variant of CDC42 (P60953)
L20V (p.Leu20Val) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
L20V (p.Leu20Val) variant details
- p.Leu20Val
- gnomAD 1-22078747-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.289
- CADD 15.80
- Most common in the Middle Eastern population (allele frequency 0.0007)
- Structural context available
- Literature evidence available