E40D (p.Glu40Asp) variant of FBXW7 (Q969H0)
E40D (p.Glu40Asp) in FBXW7 (Q969H0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
E40D (p.Glu40Asp) variant details
- p.Glu40Asp
- Ensembl rs1737982766
- Missense
- Variant Prioritization Score for Impact Estimate 0.505
- CADD 20.90
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available