Variant · Snv
TGFBI NM_000358.3(TGFBI):c.1411-3C>T
CI-VAR-00051313Explore in graph →NM_000358.3:c.1411-3C>TClinVar 350888 rs11242308
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 |
|---|---|---|---|---|---|---|---|---|
| 350888 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Corneal dystrophy; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Cervical cancer; Colon adenocarcinoma; Colorectal cancer; Uterine carcinosarcoma; Thymoma; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Lung cancer; Ovarian cancer | germline | 3 | Jan 17, 2026 | clinvar |