E89D (p.Glu89Asp) variant of PLP1 (Myelin proteolipid protein)
E89D (p.Glu89Asp) in PLP1 (Myelin proteolipid protein) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E89D (p.Glu89Asp) variant details
- p.Glu89Asp
- TOPMed rs11543024
- gnomAD rs11543024
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available