Variant · Snv
CAPN5 NM_004055.5(CAPN5):c.1740+5G>C
CI-VAR-00196249Explore in graph →NM_004055.5:c.1740+5G>CClinVar 1167065 rs59430193
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 |
|---|---|---|---|---|---|---|---|---|
| 1167065 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Colorectal cancer; Cholangiocarcinoma; Adrenocortical carcinoma, hereditary; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Lymphoma; Nonpapillary renal cell carcinoma | germline | 5 | Feb 03, 2026 | clinvar |