R13G (p.Arg13Gly) variant of FBXW7 (Q969H0)
R13G (p.Arg13Gly) in FBXW7 (Q969H0) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R13G (p.Arg13Gly) variant details
- p.Arg13Gly
- gnomAD rs781123562
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available