R41G (p.Arg41Gly) variant of RAF1 (P04049)
R41G (p.Arg41Gly) in RAF1 (P04049) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data, experimental measurements, and structural context.
R41G (p.Arg41Gly) variant details
- p.Arg41Gly
- TOPMed rs1480507957
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- RAF1 Raf-like Ras-binding domain domainome 1.0: score -1.03