G47G (p.Gly47Gly) variant of CDC42 (P60953)
G47G (p.Gly47Gly) in CDC42 (P60953) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
G47G (p.Gly47Gly) variant details
- p.Gly47Gly
- rs991706001
- gnomAD 1-22078776-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.322
- CADD 20.40
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available