E38D (p.Glu38Asp) variant of FBXW7 (Q969H0)
E38D (p.Glu38Asp) in FBXW7 (Q969H0) is a missense change. The record also includes structural context.
E38D (p.Glu38Asp) variant details
- p.Glu38Asp
- TOPMed rs1026105131
- Missense
- Structural context available
E38D (p.Glu38Asp) in FBXW7 (Q969H0) is a missense change. The record also includes structural context.