Variant · Deletion
CAPN15 NM_005632.3(CAPN15):c.3083+5_3083+40del
CI-VAR-00306057Explore in graph →NM_005632.3:c.3083+5_3083+40delClinVar 2645822 rs1441582052
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 |
|---|---|---|---|---|---|---|---|---|
| 2645822 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | CAPN15-related disorder; Oculogastrointestinal-neurodevelopmental syndrome; Adrenocortical carcinoma, hereditary | germline | 4 | Jun 01, 2026 | clinvar |