R29W (p.Arg29Trp) variant of LRP4 (O75096)
R29W (p.Arg29Trp) in LRP4 (O75096) 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 population frequency data and structural context.
R29W (p.Arg29Trp) variant details
- p.Arg29Trp
- ESP rs146259656
- ExAC rs146259656
- TOPMed rs146259656
- gnomAD rs146259656
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Population evidence available
- Structural context available