G38V (p.Gly38Val) variant of TSC1 (Hamartin)
G38V (p.Gly38Val) in TSC1 (Hamartin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Tuberous sclerosis 1. The record also includes structural context.
G38V (p.Gly38Val) variant details
- p.Gly38Val
- Ensembl rs2132271039
- Uncertain significance
- Tuberous sclerosis 1
- Missense
- ClinVar: Uncertain significance (Tuberous sclerosis 1)
- UniProt: Uncertain significance
- Structural context available