CCNB3 — 147 ClinVar variants

All ClinVar germline CCNB3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 122 flagged for review →

1 Pathogenic · 4 Likely pathogenic · 3 Conflicting · 5 Benign · 25 Likely benign · 109 Uncertain significance

Full CCNB3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 122

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 5

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

Predictors lean, ClinVar uncertain 48

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

Predictors split 69

The independent predictors disagree with each other — read with care.

All CCNB3 variants

Pathogenic 1

  • p.Val1251Asp No assertion criteria pregnancy loss, recurrent, susceptibility to, 1 ⚠

Likely pathogenic 4

Conflicting classifications of pathogenicity 3

Benign 5

Likely benign 25

Uncertain significance 109