D38D (p.Asp38Asp) variant of CDC42 (P60953)
D38D (p.Asp38Asp) in CDC42 (P60953) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
D38D (p.Asp38Asp) variant details
- p.Asp38Asp
- gnomAD 1-22078779-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.237
- CADD 12.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available