S71P (p.Ser71Pro) variant of CDC42 (P60953)
S71P (p.Ser71Pro) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data, published literature, and structural context.
S71P (p.Ser71Pro) variant details
- p.Ser71Pro
- gnomAD 1-22078828-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.733
- CADD 18.50
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available
- Literature evidence available