S71C (p.Ser71Cys) variant of CDC42 (P60953)
S71C (p.Ser71Cys) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
S71C (p.Ser71Cys) variant details
- p.Ser71Cys
- gnomAD 1-22078814-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- CADD 12.70
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available