Variant · Snv
TGFBI NM_000358.3(TGFBI):c.1803G>A (p.Leu601=)
CI-VAR-00051314Explore in graph →p.Leu601=NM_000358.3:c.1803G>AClinVar 350894 rs35151677
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 |
|---|---|---|---|---|---|---|---|---|
| 350894 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Corneal dystrophy; Clear cell carcinoma of kidney; Colon adenocarcinoma; Colorectal cancer; Ovarian serous cystadenocarcinoma; Lung cancer; Ovarian cancer; Uterine carcinosarcoma; Hepatocellular carcinoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus | germline | 3 | Jan 17, 2026 | clinvar |