T26S (p.Thr26Ser) variant of TSC1 (Hamartin)
T26S (p.Thr26Ser) in TSC1 (Hamartin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
T26S (p.Thr26Ser) variant details
- p.Thr26Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available