Variant · Snv
TGFBR2 NM_003242.6(TGFBR2):c.412T>G (p.Cys138Gly)
CI-VAR-00033221Explore in graph →p.Cys138GlyNM_003242.6:c.412T>GClinVar 213915 rs863223838
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 |
|---|---|---|---|---|---|---|---|---|
| 213915 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Familial thoracic aortic aneurysm and aortic dissection; Congenital aneurysm of ascending aorta; Loeys-Dietz syndrome; Loeys-Dietz syndrome 2; Malignant tumor of esophagus; Colorectal cancer, hereditary nonpolyposis, type 6; Diabetic retinopathy | germline | 8 | Feb 13, 2025 | clinvar |