Q25H (p.Gln25His) variant of MCM5 (P33992)
Q25H (p.Gln25His) in MCM5 (P33992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
Q25H (p.Gln25His) variant details
- p.Gln25His
- gnomAD 22-35400513-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.27
- REVEL 0.08
- CADD 21.20
- PolyPhen-2 0.00
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available