Variant · Snv
TOR1A NM_000113.3(TOR1A):c.749-11C>A
CI-VAR-00047305Explore in graph →NM_000113.3:c.749-11C>AClinVar 255137 rs72755217
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 255137 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Early-onset generalized limb-onset dystonia; Dystonic disorder; Uterine corpus endometrial carcinoma; Sarcoma; Lymphoma; Malignant tumor of esophagus; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Gastric cancer; Lung cancer; Ovarian cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia | germline | 9 | Jan 21, 2026 | clinvar |