G109D (p.Gly109Asp) variant of DMD (Dystrophin)
G109D (p.Gly109Asp) in DMD (Dystrophin) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
G109D (p.Gly109Asp) variant details
- p.Gly109Asp
- TOPMed rs1048652498
- gnomAD rs1048652498
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available