C57G (p.Cys57Gly) variant of TNFAIP3 (P21580)
C57G (p.Cys57Gly) in TNFAIP3 (P21580) is a missense change. The record also includes structural context.
C57G (p.Cys57Gly) variant details
- p.Cys57Gly
- TOPMed rs1776056180
- Missense
- Structural context available