Variant · Deletion
SEPSECS NM_016955.4(SEPSECS):c.115-4del
CI-VAR-00201318Explore in graph →NM_016955.4:c.115-4delClinVar 1296157 rs34423002
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 |
|---|---|---|---|---|---|---|---|---|
| 1296157 | Benign | criteria provided, single submitter | 1 | Pontocerebellar hypoplasia type 2D; Gastric cancer; Cholangiocarcinoma; Familial cancer of breast; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Papillary renal cell carcinoma type 1; Malignant tumor of esophagus | germline | 3 | Aug 10, 2019 | clinvar |