Variant · Snv
SUN1 NM_001130965.3(SUN1):c.452-12T>G
CI-VAR-00227248Explore in graph →NM_001130965.3:c.452-12T>GClinVar 1587240 rs201328717
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 |
|---|---|---|---|---|---|---|---|---|
| 1587240 | Benign | criteria provided, single submitter | 1 | Emery-Dreifuss muscular dystrophy; Hepatocellular carcinoma; Malignant tumor of esophagus; Germ cell tumor of testis; Lung cancer; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Familial pancreatic carcinoma; Sarcoma; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Cervical cancer; Ovarian cancer; Gastric cancer; Uterine carcinosarcoma; Familial cancer of breast | germline | 2 | Jan 27, 2026 | clinvar |