V42D (p.Val42Asp) variant of CDC42 (P60953)
V42D (p.Val42Asp) in CDC42 (P60953) is a missense 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.
V42D (p.Val42Asp) variant details
- p.Val42Asp
- gnomAD 1-22078766-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- CADD 17.30
- Most common in the HGDP:BURUSHO population (allele frequency 0.042)
- Structural context available
- Literature evidence available