p.Ala19 Gln20insArgGlyAspAla variant of MCM5 (P33992)
p.Ala19 Gln20insArgGlyAspAla in MCM5 (P33992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data, published literature, and structural context.
p.Ala19 Gln20insArgGlyAspAla variant details
- gnomAD 22-35400484-G-GGG
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.719
- CADD 22.60
- Population evidence available
- Structural context available
- Literature evidence available