Variant · Snv
SH3BP2 NM_001122681.2(SH3BP2):c.1407-11T>A
CI-VAR-00051154Explore in graph →NM_001122681.2:c.1407-11T>AClinVar 348591 rs45525837
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 |
|---|---|---|---|---|---|---|---|---|
| 348591 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Fibrous dysplasia of jaw; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Uveal melanoma; Lymphoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Familial pancreatic carcinoma; Ovarian serous cystadenocarcinoma | germline | 4 | Feb 02, 2026 | clinvar |