Variant · Snv
SF3B1 NM_012433.4(SF3B1):c.2078-8T>A
CI-VAR-00339117Explore in graph →NM_012433.4:c.2078-8T>AClinVar 3041954 rs3764989
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 |
|---|---|---|---|---|---|---|---|---|
| 3041954 | Likely benign | no assertion criteria provided | 0 | SF3B1-related disorder; Sarcoma; Gastric cancer; Lymphoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Germ cell tumor of testis; Uterine corpus endometrial carcinoma; Familial pancreatic carcinoma; Uterine carcinosarcoma; Lung cancer; Cervical cancer; Familial cancer of breast; Ovarian cancer; Malignant tumor of esophagus | germline | 2 | Apr 25, 2019 | clinvar |