TTC14 — 105 ClinVar variants

All ClinVar germline TTC14 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 90 flagged for review →

3 Benign · 9 Likely benign · 93 Uncertain significance

Full TTC14 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 90

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 80

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

All TTC14 variants

Benign 3

  • c.287-3dup No assertion criteria TTC14-related disorder
  • p.Ala352= No assertion criteria TTC14-related disorder
  • p.Ser296= No assertion criteria TTC14-related disorder

Likely benign 9

Uncertain significance 93