Variant · Snv
TGFB1 NM_000660.7(TGFB1):c.355+5G>A
CI-VAR-00126214Explore in graph →NM_000660.7:c.355+5G>AClinVar 978501 rs11466318
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 |
|---|---|---|---|---|---|---|---|---|
| 978501 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Diaphyseal dysplasia; Inflammatory bowel disease, immunodeficiency, and encephalopathy; Cystic fibrosis; Cervical cancer; Gastric cancer; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Sarcoma; Uterine carcinosarcoma | germline | 5 | Feb 02, 2026 | clinvar |