APOBEC3B — 54 ClinVar variants

All ClinVar germline APOBEC3B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 44 flagged for review →

1 Conflicting · 3 Benign · 1 Benign/Likely benign · 8 Likely benign · 41 Uncertain significance

Full APOBEC3B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 44

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 21

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

All APOBEC3B variants

Conflicting classifications of pathogenicity 1

Benign 3

Benign/Likely benign 1

  • p.Ser109Ala Multiple submitters APOBEC3B-related condition

Likely benign 8

Uncertain significance 41