Variant · Snv
TGFBR1 NM_004612.4(TGFBR1):c.346A>G (p.Lys116Glu)
CI-VAR-00156902Explore in graph →p.Lys116GluNM_004612.4:c.346A>GClinVar 926107 rs1827266142
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 |
|---|---|---|---|---|---|---|---|---|
| 926107 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Familial thoracic aortic aneurysm and aortic dissection; Ovarian serous cystadenocarcinoma | germline | 3 | Jun 17, 2021 | clinvar |