G28V (p.Gly28Val) variant of TNFRSF4 (P43489)
G28V (p.Gly28Val) in TNFRSF4 (P43489) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance.
G28V (p.Gly28Val) variant details
- p.Gly28Val
- TOPMed rs867902887
- gnomAD rs867902887
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance