CDC42BPG — 295 ClinVar variants

All ClinVar germline CDC42BPG variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 273 flagged for review →

4 Benign · 22 Likely benign · 269 Uncertain significance

Full CDC42BPG gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 273

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 lean, ClinVar uncertain 134

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

Predictors split 139

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

All CDC42BPG variants

Benign 4

Likely benign 22

Uncertain significance 269