Q74H (p.Gln74His) variant of CDC42 (P60953)
Q74H (p.Gln74His) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
Q74H (p.Gln74His) variant details
- p.Gln74His
- rs761966253
- gnomAD 1-22078848-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- CADD 8.96
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available