Variant · Other
AEBP1 NM_001129.5(AEBP1):c.1018+4_1018+7del
CI-VAR-00134680Explore in graph →NM_001129.5:c.1018+4_1018+7delClinVar 810089 rs376965157
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 |
|---|---|---|---|---|---|---|---|---|
| 810089 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | AEBP1-related disorder; Colon adenocarcinoma; Gastric cancer; Lymphoma; Papillary renal cell carcinoma type 1; Melanoma; Ovarian cancer; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Familial cancer of breast | germline | 9 | Apr 01, 2026 | clinvar |