Variant · Deletion
VCL NM_014000.3(VCL):c.169-11del
CI-VAR-00093602Explore in graph →NM_014000.3:c.169-11delClinVar 506391 rs753900484
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 506391 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Dilated cardiomyopathy 1W; Hypertrophic cardiomyopathy 15; Familial cancer of breast; Colon adenocarcinoma | germline | 4 | Nov 22, 2025 | clinvar |