CLLU1-AS1 — 11 ClinVar variants
All ClinVar germline CLLU1-AS1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 10 flagged for review →
1 Likely benign · 10 Uncertain significance
Full CLLU1-AS1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 10
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 10
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
- CLLU1-AS1 n.119C>G Uncertain significance Single submitter
- CLLU1-AS1 n.121C>G Uncertain significance Single submitter
- CLLU1-AS1 n.126C>G Uncertain significance Single submitter
- CLLU1-AS1 n.166G>A Uncertain significance Single submitter
- CLLU1-AS1 n.177G>A Uncertain significance Single submitter
- CLLU1-AS1 n.223A>T Uncertain significance Single submitter
- CLLU1-AS1 n.235A>G Uncertain significance Single submitter
- CLLU1-AS1 n.243G>A Uncertain significance Single submitter
- CLLU1-AS1 n.63C>G Uncertain significance Single submitter
- CLLU1-AS1 n.97T>G Uncertain significance Single submitter
All CLLU1-AS1 variants
Likely benign 1
- n.169C>T Single submitter