P36L (p.Pro36Leu) variant of KDM6B (Lysine-specific demethylase 6B)
P36L (p.Pro36Leu) in KDM6B (Lysine-specific demethylase 6B) 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.
P36L (p.Pro36Leu) variant details
- p.Pro36Leu
- NCI-TCGA TCGA novel
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available