Variant · Snv
EXO1 NM_130398.4(EXO1):c.2212-1G>C
CI-VAR-00127862Explore in graph →NM_130398.4:c.2212-1G>CClinVar 708631 rs4150000
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 |
|---|---|---|---|---|---|---|---|---|
| 708631 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | EXO1-related disorder; Familial cancer of breast; Ovarian cancer; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Acute myeloid leukemia; Lung cancer; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer; Ovarian serous cystadenocarcinoma; Melanoma | germline | 5 | Nov 06, 2024 | clinvar |