S71A (p.Ser71Ala) variant of CDC42 (P60953)
S71A (p.Ser71Ala) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
S71A (p.Ser71Ala) variant details
- p.Ser71Ala
- gnomAD 1-22078813-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- CADD 8.92
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available