MOBP — 19 ClinVar variants

All ClinVar germline MOBP variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 9 flagged for review →

7 Likely benign · 12 Uncertain significance

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

⚑ Evidence disagreements 9

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 3

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

All MOBP variants

Likely benign 7

  • c.207-27G>A Single submitter MOBP-related disorder
  • p.99SPPRSERQPR[3] No assertion criteria MOBP-related disorder
  • p.Lys96= No assertion criteria MOBP-related disorder
  • p.Pro121Ser No assertion criteria MOBP-related disorder ⚠
  • p.Pro152= No assertion criteria MOBP-related disorder
  • p.Pro80= No assertion criteria MOBP-related disorder
  • p.Ser19= No assertion criteria MOBP-related disorder

Uncertain significance 12