W119* (p.Trp119Ter) variant of MAOB (P27338)
W119* (p.Trp119Ter) in MAOB (P27338) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
W119* (p.Trp119Ter) variant details
- p.Trp119Ter
- NCI-TCGA Cosmic COSV6520
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.
- Structural context available