P34S (p.Pro34Ser) variant of CDC42 (P60953)
P34S (p.Pro34Ser) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data, published literature, and structural context.
P34S (p.Pro34Ser) variant details
- p.Pro34Ser
- gnomAD 1-22078578-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.768
- CADD 25.20
- PolyPhen-2 0.55
- SIFT 0.02
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available