G66W (p.Gly66Trp) variant of MCM5 (P33992)
G66W (p.Gly66Trp) in MCM5 (P33992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
G66W (p.Gly66Trp) variant details
- p.Gly66Trp
- gnomAD 22-35401420-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- CADD 5.74
- Population evidence available
- Structural context available
- Literature evidence available