Variant · Snv
TARS1 NM_152295.5(TARS1):c.693+6T>C
CI-VAR-00339265Explore in graph →NM_152295.5:c.693+6T>CClinVar 3056225 rs75319890
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 |
|---|---|---|---|---|---|---|---|---|
| 3056225 | Benign | no assertion criteria provided | 0 | TARS1-related disorder; Familial pancreatic carcinoma; Lymphoma; Acute myeloid leukemia; Ovarian cancer; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Gastric cancer; Thymoma | germline | 2 | Nov 18, 2019 | clinvar |