S13C (p.Ser13Cys) variant of TNFAIP3 (P21580)
S13C (p.Ser13Cys) in TNFAIP3 (P21580) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
S13C (p.Ser13Cys) variant details
- p.Ser13Cys
- gnomAD rs1470990172
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available