Variant · Other
EZR NM_001111077.2(EZR):c.97-18TC[5]
CI-VAR-00132354Explore in graph →NM_001111077.2:c.97-18TC[5]ClinVar 779916 rs150994217
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 |
|---|---|---|---|---|---|---|---|---|
| 779916 | Benign | criteria provided, single submitter | 1 | Glioma susceptibility 1; Nonpapillary renal cell carcinoma; Familial cancer of breast; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Cholangiocarcinoma | germline | 2 | Jul 06, 2018 | clinvar |