Y79H (p.Tyr79His) variant of TNFRSF13B (O14836)
Y79H (p.Tyr79His) in TNFRSF13B (O14836) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
Y79H (p.Tyr79His) variant details
- p.Tyr79His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.