Y207N (p.Tyr207Asn) variant of PLP1 (Myelin proteolipid protein)
Y207N (p.Tyr207Asn) in PLP1 (Myelin proteolipid protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Pelizaeus-Merzbacher disease. The record also includes published literature and structural context.
Y207N (p.Tyr207Asn) variant details
- p.Tyr207Asn
- rs2522315532
- ClinVar RCV004595787
- Likely pathogenic
- Pelizaeus-Merzbacher disease
- Missense
- ClinVar: Likely pathogenic (Pelizaeus-Merzbacher disease)
- EBI: Likely pathogenic (in HLD1)
- UniProt: Likely pathogenic (in HLD1)
- Structural context available
- Cited in: PLP1-Related Disorders. (PMID 20301361)