V9V (p.Val9Val) variant of CDC42 (P60953)
V9V (p.Val9Val) in CDC42 (P60953) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
V9V (p.Val9Val) variant details
- p.Val9Val
- gnomAD 1-22078505-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.283
- CADD 8.25
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available