Variant · Snv
ZBTB24 NM_014797.3(ZBTB24):c.953-20T>A
CI-VAR-00170131Explore in graph →NM_014797.3:c.953-20T>AClinVar 993897 rs117893130
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 |
|---|---|---|---|---|---|---|---|---|
| 993897 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Immunodeficiency-centromeric instability-facial anomalies syndrome 2; Nonpapillary renal cell carcinoma; Cervical cancer; Ovarian cancer; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Uveal melanoma; Familial pancreatic carcinoma; Sarcoma; Gastric cancer; Lymphoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Thymoma; Malignant tumor of esophagus | germline | 3 | Feb 03, 2026 | clinvar |