E68D (p.Glu68Asp) variant of CSF3R (Q99062)
E68D (p.Glu68Asp) in CSF3R (Q99062) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E68D (p.Glu68Asp) variant details
- p.Glu68Asp
- TOPMed rs1651080055
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available