A17P (p.Ala17Pro) variant of PLP1 (Myelin proteolipid protein)
A17P (p.Ala17Pro) 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.
A17P (p.Ala17Pro) variant details
- p.Ala17Pro
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10039
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available