CCDC9B — 6 ClinVar variants
All ClinVar germline CCDC9B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 5 flagged for review →
1 Likely benign · 5 Uncertain significance
Full CCDC9B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 5
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.
Predictors split 2
The independent predictors disagree with each other — read with care.
All CCDC9B variants
Likely benign 1
- p.Gly67= Single submitter
Uncertain significance 5
- p.Arg462Gln Single submitter ⚠
- p.Asp202Gly Single submitter ⚠
- p.His2Leu Single submitter ⚠
- p.Leu260Met Single submitter ⚠
- p.Val428Ile Single submitter ⚠