Variant · Deletion
SEC63 NM_007214.5(SEC63):c.340-9_340-7del
CI-VAR-00051179Explore in graph →NM_007214.5:c.340-9_340-7delClinVar 354913 rs66526324
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 |
|---|---|---|---|---|---|---|---|---|
| 354913 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Polycystic liver disease 2; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Lymphoma; Hepatocellular carcinoma; Ovarian cancer; Cholangiocarcinoma; Nonpapillary renal cell carcinoma | germline | 3 | Jan 19, 2026 | clinvar |