CDC25A — 48 ClinVar variants

All ClinVar germline CDC25A variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 43 flagged for review →

1 Likely pathogenic · 1 Benign · 5 Likely benign · 41 Uncertain significance

Full CDC25A gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 43

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

Predictors vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

Predictors lean, ClinVar uncertain 32

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All CDC25A variants

Likely pathogenic 1

  • p.Ser88Phe No assertion criteria autosomal dominant polycystic liver disease ⚠

Benign 1

Likely benign 5

Uncertain significance 41