F26L (p.Phe26Leu) variant of PLP1 (Myelin proteolipid protein)
F26L (p.Phe26Leu) in PLP1 (Myelin proteolipid protein) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F26L (p.Phe26Leu) variant details
- p.Phe26Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available