TRIM28 — 291 ClinVar variants

All ClinVar germline TRIM28 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 113 flagged for review →

9 Pathogenic · 5 Likely pathogenic · 1 Conflicting · 25 Benign · 6 Benign/Likely benign · 108 Likely benign · 137 Uncertain significance

Full TRIM28 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 113

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 88

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

Predictors split 24

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

All TRIM28 variants

Pathogenic 9

Likely pathogenic 5

Conflicting classifications of pathogenicity 1

Benign 25

Benign/Likely benign 6

Likely benign 108

Uncertain significance 137