E39G (p.Glu39Gly) variant of FBXW7 (Q969H0)
E39G (p.Glu39Gly) in FBXW7 (Q969H0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
E39G (p.Glu39Gly) variant details
- p.Glu39Gly
- TOPMed rs1036262056
- gnomAD rs1036262056
- Missense
- Variant Prioritization Score for Impact Estimate 0.346
- REVEL 0.16
- CADD 24.50
- PolyPhen-2 0.00
- SIFT 0.00
- Population evidence available
- Structural context available