Variant · Snv
AARS2 NM_020745.4(AARS2):c.1753-14C>G
CI-VAR-00051621Explore in graph →NM_020745.4:c.1753-14C>GClinVar 357065 rs74950428
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 |
|---|---|---|---|---|---|---|---|---|
| 357065 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Combined oxidative phosphorylation defect type 8; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Lymphoma; Uterine carcinosarcoma; Thymoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Uveal melanoma; Hepatocellular carcinoma; Ovarian cancer | germline | 5 | Feb 01, 2026 | clinvar |