APOBEC3G — 38 ClinVar variants

All ClinVar germline APOBEC3G variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 37 flagged for review →

2 Likely benign · 36 Uncertain significance

Full APOBEC3G gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 37

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 24

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

All APOBEC3G variants

Likely benign 2

Uncertain significance 36