Variant · Snv
CCNO NM_021147.5(CCNO):c.382-14C>G
CI-VAR-00058626Explore in graph →NM_021147.5:c.382-14C>GClinVar 402509 rs72749883
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 402509 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Primary ciliary dyskinesia; Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma; Nonpapillary renal cell carcinoma; Uveal melanoma; Lymphoma; Ovarian cancer; Familial pancreatic carcinoma | germline | 6 | Feb 04, 2026 | clinvar |