G14V (p.Gly14Val) variant of RAF1 (P04049)
G14V (p.Gly14Val) in RAF1 (P04049) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes experimental measurements and structural context.
G14V (p.Gly14Val) variant details
- p.Gly14Val
- ExAC rs757333753
- TOPMed rs757333753
- gnomAD rs757333753
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- RAF1 Raf-like Ras-binding domain domainome 1.0: score -0.289