E61D (p.Glu61Asp) variant of TGFB2 (P61812)
E61D (p.Glu61Asp) in TGFB2 (P61812) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E61D (p.Glu61Asp) variant details
- p.Glu61Asp
- ExAC rs764288352
- TOPMed rs764288352
- gnomAD rs764288352
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available