CBLL2 — 52 ClinVar variants

All ClinVar germline CBLL2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 42 flagged for review →

1 Conflicting · 4 Benign · 9 Likely benign · 38 Uncertain significance

Full CBLL2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 42

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 agree, ClinVar conflicts 1

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 35

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

All CBLL2 variants

Conflicting classifications of pathogenicity 1

Benign 4

Likely benign 9

Uncertain significance 38