L11S (p.Leu11Ser) variant of TSC2 (Tuberin)
L11S (p.Leu11Ser) in TSC2 (Tuberin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
L11S (p.Leu11Ser) variant details
- p.Leu11Ser
- NCI-TCGA TCGA novel
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available