Variant · Snv
SUN1 NM_001130965.3(SUN1):c.911-12C>G
CI-VAR-00225621Explore in graph →NM_001130965.3:c.911-12C>GClinVar 1603206 rs117540096
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1603206 | Benign | criteria provided, single submitter | 1 | Emery-Dreifuss muscular dystrophy; Lymphoma; Uterine carcinosarcoma; Thymoma; Melanoma; Uterine corpus endometrial carcinoma; Cervical cancer; Familial cancer of breast; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Gastric cancer; Cholangiocarcinoma; Malignant tumor of esophagus; Uveal melanoma; Sarcoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma | germline | 2 | Feb 01, 2026 | clinvar |