Variant · Snv
TONSL NM_013432.5(TONSL):c.448+40G>A
CI-VAR-00203776Explore in graph →NM_013432.5:c.448+40G>AClinVar 1342246 rs2242263
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1342246 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Sponastrime dysplasia; Gastric cancer; Uterine carcinosarcoma; Hepatocellular carcinoma; Lung cancer | germline | 3 | Sep 10, 2021 | clinvar |