R16G (p.Arg16Gly) variant of TNFAIP3 (P21580)
R16G (p.Arg16Gly) in TNFAIP3 (P21580) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes variant effect predictions and structural context.
R16G (p.Arg16Gly) variant details
- p.Arg16Gly
- TOPMed rs1414718116
- gnomAD rs1414718116
- Uncertain significance
- Missense
- MetaLR 0.04
- MetaSVM -1.14
- SIFT 0.22
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available