G47D (p.Gly47Asp) variant of CDC42 (P60953)
G47D (p.Gly47Asp) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
G47D (p.Gly47Asp) variant details
- p.Gly47Asp
- rs927977264
- gnomAD 1-22078775-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.408
- CADD 19.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available