DNAJC14 — 93 ClinVar variants

All ClinVar germline DNAJC14 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 91 flagged for review →

2 Likely benign · 91 Uncertain significance

Full DNAJC14 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 91

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 61

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

Predictors split 30

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

All DNAJC14 variants

Likely benign 2

  • p.Arg389Gln Multiple submitters
  • p.Gly211Glu No assertion criteria EBV-positive nodal T- and NK-cell lymphoma

Uncertain significance 91