E41V (p.Glu41Val) variant of MBP (Myelin basic protein)
E41V (p.Glu41Val) in MBP (Myelin basic protein) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E41V (p.Glu41Val) variant details
- p.Glu41Val
- NCI-TCGA Cosmic COSV6355
- cosmic curated COSV63556
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available