P106H (p.Pro106His) variant of LRP4 (O75096)
P106H (p.Pro106His) in LRP4 (O75096) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes population frequency data and structural context.
P106H (p.Pro106His) variant details
- p.Pro106His
- NCI-TCGA TCGA novel
- 1000Genomes rs556889686
- ExAC rs556889686
- TOPMed rs556889686
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available