G47V (p.Gly47Val) variant of CDC42 (P60953)
G47V (p.Gly47Val) in CDC42 (P60953) is a missense 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.
G47V (p.Gly47Val) variant details
- p.Gly47Val
- rs927977264
- gnomAD 1-22078775-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- CADD 18.90
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available
- Literature evidence available