C18C (p.Cys18Cys) variant of CDC42 (P60953)
C18C (p.Cys18Cys) in CDC42 (P60953) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
C18C (p.Cys18Cys) variant details
- p.Cys18Cys
- gnomAD 1-22078532-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.397
- CADD 13.70
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available