M18C (p.Met18Cys) variant of TSC1 (Hamartin)
M18C (p.Met18Cys) 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.
M18C (p.Met18Cys) variant details
- p.Met18Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available