G69R (p.Gly69Arg) variant of MCM2 (P49736)
G69R (p.Gly69Arg) in MCM2 (P49736) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
G69R (p.Gly69Arg) variant details
- p.Gly69Arg
- gnomAD 3-127599516-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.582
- REVEL 0.46
- MetaLR 0.44
- MetaSVM 0.02
- CADD 33.00
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available