Variant · Snv
SCN1B NM_001037.5(SCN1B):c.591-25T>G
CI-VAR-00200943Explore in graph →NM_001037.5:c.591-25T>GClinVar 1285019 rs28365107
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 |
|---|---|---|---|---|---|---|---|---|
| 1285019 | Benign | criteria provided, single submitter | 1 | Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Uveal melanoma; Sarcoma; Thymoma; Acute myeloid leukemia | germline | 4 | — | clinvar |