E67S (p.Glu67Ser) variant of MCM5 (P33992)
E67S (p.Glu67Ser) in MCM5 (P33992) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
E67S (p.Glu67Ser) variant details
- p.Glu67Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available