Q142K (p.Gln142Lys) variant of LRP4 (O75096)
Q142K (p.Gln142Lys) 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 structural context.
Q142K (p.Gln142Lys) variant details
- p.Gln142Lys
- gnomAD rs1246644250
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available