R32G (p.Arg32Gly) variant of MTOR (P42345)
R32G (p.Arg32Gly) in MTOR (P42345) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R32G (p.Arg32Gly) variant details
- p.Arg32Gly
- TOPMed rs1446194159
- gnomAD rs1446194159
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available