G47A (p.Gly47Ala) variant of CDC42 (P60953)
G47A (p.Gly47Ala) 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.
G47A (p.Gly47Ala) variant details
- p.Gly47Ala
- rs927977264
- gnomAD 1-22078775-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.403
- CADD 19.00
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available
- Literature evidence available