Variant · Deletion
AGBL5 NM_021831.6(AGBL5):c.552-9del
CI-VAR-00232288Explore in graph →NM_021831.6:c.552-9delClinVar 1586121 rs368758886
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 |
|---|---|---|---|---|---|---|---|---|
| 1586121 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Colorectal cancer; Nonpapillary renal cell carcinoma; Colon adenocarcinoma; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast | germline | 3 | Nov 20, 2024 | clinvar |