DUSP22 — 55 ClinVar variants

All ClinVar germline DUSP22 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 35 flagged for review →

3 Benign · 20 Likely benign · 32 Uncertain significance

Full DUSP22 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 35

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All DUSP22 variants

Benign 3

Likely benign 20

  • p.Asn128= Single submitter
  • p.Val129Leu Single submitter
  • c.189-4C>T No assertion criteria DUSP22-related disorder
  • c.56-6dup No assertion criteria DUSP22-related disorder
  • c.-5C>T No assertion criteria DUSP22-related disorder
  • c.*1871C>G No assertion criteria DUSP22-related disorder
  • c.*2G>A No assertion criteria DUSP22-related disorder
  • c.*8G>A No assertion criteria DUSP22-related disorder
  • p.Ala23= No assertion criteria DUSP22-related disorder
  • p.Ala56= No assertion criteria DUSP22-related disorder
  • p.His75= No assertion criteria DUSP22-related disorder
  • p.Leu159Phe No assertion criteria DUSP22-related disorder ⚠
  • p.Leu51= No assertion criteria DUSP22-related disorder
  • p.Pro195Leu No assertion criteria DUSP22-related disorder
  • p.Ser95= No assertion criteria DUSP22-related disorder
  • p.Thr105= No assertion criteria DUSP22-related disorder
  • p.Thr202= No assertion criteria DUSP22-related disorder
  • p.Tyr198= No assertion criteria DUSP22-related disorder
  • p.Val106Ile No assertion criteria DUSP22-related disorder ⚠
  • p.Val143Ile No assertion criteria DUSP22-related disorder ⚠

Uncertain significance 32