L186M (p.Leu186Met) variant of MAOB (P27338)
L186M (p.Leu186Met) in MAOB (P27338) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L186M (p.Leu186Met) variant details
- p.Leu186Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available