Y79* (p.Tyr79Ter) variant of TNFRSF13B (O14836)
Y79* (p.Tyr79Ter) in TNFRSF13B (O14836) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
Y79* (p.Tyr79Ter) variant details
- p.Tyr79Ter
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.