E38G (p.Glu38Gly) variant of FBXW7 (Q969H0)
E38G (p.Glu38Gly) in FBXW7 (Q969H0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
E38G (p.Glu38Gly) variant details
- p.Glu38Gly
- ExAC rs758603153
- TOPMed rs758603153
- gnomAD rs758603153
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.25
- CADD 24.80
- PolyPhen-2 0.10
- SIFT 0.00
- Population evidence available
- Structural context available