CCNB1 — 52 ClinVar variants

All ClinVar germline CCNB1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 50 flagged for review →

2 Likely benign · 50 Uncertain significance

Full CCNB1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 50

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 split 29

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

All CCNB1 variants

Likely benign 2

Uncertain significance 50