G112C (p.Gly112Cys) variant of TNFRSF4 (P43489)
G112C (p.Gly112Cys) in TNFRSF4 (P43489) is a missense change. The record also includes structural context.
G112C (p.Gly112Cys) variant details
- p.Gly112Cys
- TOPMed rs1649249051
- Missense
- Structural context available