LENG8 — 145 ClinVar variants

All ClinVar germline LENG8 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 124 flagged for review →

1 Conflicting · 5 Benign · 13 Likely benign · 126 Uncertain significance

Full LENG8 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 124

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 109

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

All LENG8 variants

Conflicting classifications of pathogenicity 1

Benign 5

  • c.1732-9C>T No assertion criteria LENG8-related disorder
  • p.Arg430Cys No assertion criteria LENG8-related disorder
  • p.Gln85His No assertion criteria LENG8-related disorder
  • p.Ile557Val No assertion criteria LENG8-related disorder
  • p.Ile630= No assertion criteria LENG8-related disorder

Likely benign 13

  • c.*438C>T Single submitter
  • p.Ala486= Single submitter
  • p.Gly57Ser Single submitter
  • p.Thr384= Single submitter
  • p.Ala597= No assertion criteria LENG8-related disorder
  • p.Arg616= No assertion criteria LENG8-related disorder
  • p.Gly464= No assertion criteria LENG8-related disorder
  • p.His34= No assertion criteria LENG8-related disorder
  • p.Leu325= No assertion criteria LENG8-related disorder
  • p.Pro198= No assertion criteria LENG8-related disorder
  • p.Pro341= No assertion criteria LENG8-related disorder
  • p.Pro750= No assertion criteria LENG8-related disorder
  • p.Thr645= No assertion criteria LENG8-related disorder

Uncertain significance 126