NUDC — 48 ClinVar variants

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

1 Likely benign · 47 Uncertain significance

Full NUDC 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 lean, ClinVar uncertain 33

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

All NUDC variants

Likely benign 1

  • p.Ile202= No assertion criteria NUDC-related condition

Uncertain significance 47