T21I (p.Thr21Ile) variant of TGM1 (P22735)
T21I (p.Thr21Ile) in TGM1 (P22735) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
T21I (p.Thr21Ile) variant details
- p.Thr21Ile
- TOPMed rs2040820632
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available