Variant · Snv
RECQL4 NM_004260.4(RECQL4):c.3393+9A>G
CI-VAR-00047288Explore in graph →NM_004260.4:c.3393+9A>GClinVar 259260 rs4251692
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 |
|---|---|---|---|---|---|---|---|---|
| 259260 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Baller-Gerold syndrome; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Ovarian cancer; Uterine corpus endometrial carcinoma; Uveal melanoma; Lymphoma; Uterine carcinosarcoma; Cholangiocarcinoma; Cervical cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Sarcoma; Gastric cancer | germline | 8 | Nov 27, 2025 | clinvar |