Variant · Other
RPL9 NM_000661.5(RPL9):c.259-10_259-7del
CI-VAR-00285105Explore in graph →NM_000661.5:c.259-10_259-7delClinVar 2039467 rs142648868
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 |
|---|---|---|---|---|---|---|---|---|
| 2039467 | Benign | criteria provided, single submitter | 1 | Familial pancreatic carcinoma; Colon adenocarcinoma; Malignant tumor of esophagus; Ovarian cancer; Colorectal cancer; Gastric cancer; Lymphoma; Cholangiocarcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Nonpapillary renal cell carcinoma | germline | 2 | Feb 04, 2026 | clinvar |