Variant · Deletion
SKIC3 NM_014639.4(SKIC3):c.3015-4del
CI-VAR-00134845Explore in graph →NM_014639.4:c.3015-4delClinVar 810934 rs745805590
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 |
|---|---|---|---|---|---|---|---|---|
| 810934 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Adrenocortical carcinoma, hereditary; Cervical cancer; Uterine corpus endometrial carcinoma; Gastric cancer; Malignant tumor of esophagus; Uveal melanoma; Cholangiocarcinoma | germline | 3 | Nov 23, 2025 | clinvar |