R12G (p.Arg12Gly) variant of FTO (Q9C0B1)
R12G (p.Arg12Gly) in FTO (Q9C0B1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
R12G (p.Arg12Gly) variant details
- p.Arg12Gly
- TOPMed rs1971815489
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available