Variant · Snv
CNTNAP2 NM_014141.6(CNTNAP2):c.3476-15C>A
CI-VAR-00047263Explore in graph →NM_014141.6:c.3476-15C>AClinVar 260349 rs77706740
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 |
|---|---|---|---|---|---|---|---|---|
| 260349 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Cortical dysplasia-focal epilepsy syndrome; Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Malignant tumor of esophagus; Germ cell tumor of testis; Gastric cancer; Lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Cholangiocarcinoma | germline | 7 | Feb 03, 2026 | clinvar |