DNAAF9 — 5 ClinVar variants
All ClinVar germline DNAAF9 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 5 flagged for review →
1 Likely benign · 4 Uncertain significance
Full DNAAF9 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 DNAAF9 variants
Likely benign 1
- p.Arg692Trp Single submitter ⚠
Uncertain significance 4
- p.Gly262Ala Single submitter ⚠
- p.Ser150Gly Single submitter ⚠
- p.Val105Ile Single submitter ⚠
- p.Val977Ile Single submitter ⚠