L21P (p.Leu21Pro) variant of TSC2 (Tuberin)
L21P (p.Leu21Pro) in TSC2 (Tuberin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided; Tuberous sclerosis 2; Hereditary cancer-predisposing syndrome. The record also includes structural context.
L21P (p.Leu21Pro) variant details
- p.Leu21Pro
- NCI-TCGA TCGA novel
- Uncertain significance
- not provided; Tuberous sclerosis 2; Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (not provided; Tuberous sclerosis 2; Hereditary cancer-predisposi)
- UniProt: Uncertain significance
- Structural context available