L57M (p.Leu57Met) variant of CUX1 (Homeobox protein cut-like 1)
L57M (p.Leu57Met) in CUX1 (Homeobox protein cut-like 1) 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 experimental measurements and structural context.
L57M (p.Leu57Met) variant details
- p.Leu57Met
- TOPMed rs1820261122
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available
- CUX1 CUT domain domainome 1.0: score -0.528