Variant · Snv
USP45 NM_001346022.3(USP45):c.845+2T>C
CI-VAR-00132135Explore in graph →NM_001346022.3:c.845+2T>CClinVar 770177 rs17850034
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 |
|---|---|---|---|---|---|---|---|---|
| 770177 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Uveal melanoma; Familial pancreatic carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1; Sarcoma; Lymphoma; Melanoma; Acute myeloid leukemia; Familial cancer of breast; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Gastric cancer; Cholangiocarcinoma; Hepatocellular carcinoma; Cervical cancer; Ovarian cancer | germline | 3 | Feb 01, 2023 | clinvar |