F51L (p.Phe51Leu) variant of PLP1 (Myelin proteolipid protein)
F51L (p.Phe51Leu) in PLP1 (Myelin proteolipid protein) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in HLD1. The record also includes structural context.
F51L (p.Phe51Leu) variant details
- p.Phe51Leu
- NCI-TCGA Cosmic COSV5827
- cosmic curated COSV58277
- Variant assessed as somatic; moderate impact.
- in HLD1
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in HLD1)
- Structural context available