C50G (p.Cys50Gly) variant of TNFRSF13B (O14836)
C50G (p.Cys50Gly) in TNFRSF13B (O14836) is a missense change.
C50G (p.Cys50Gly) variant details
- p.Cys50Gly
- ExAC rs778514858
- TOPMed rs778514858
- gnomAD rs778514858
- Missense
C50G (p.Cys50Gly) in TNFRSF13B (O14836) is a missense change.