Variant · Snv
IARS2 NM_018060.4(IARS2):c.1726A>G (p.Lys576Glu)
CI-VAR-00055951Explore in graph →p.Lys576GluNM_018060.4:c.1726A>GClinVar 380077 rs78770848
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 |
|---|---|---|---|---|---|---|---|---|
| 380077 | Benign | criteria provided, multiple submitters, no conflicts | 2 | IARS2-related disorder; Nonpapillary renal cell carcinoma; Cervical cancer; Ovarian cancer; Uterine carcinosarcoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Thyroid cancer, nonmedullary, 1; Colon adenocarcinoma; Sarcoma; Uterine corpus endometrial carcinoma; Lymphoma; Thymoma | germline | 6 | Feb 04, 2026 | clinvar |