Variant · Deletion
DDX54 NM_024072.4(DDX54):c.1939-8_1939-5del
CI-VAR-00338673Explore in graph →NM_024072.4:c.1939-8_1939-5delClinVar 3041462 rs138867026
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 |
|---|---|---|---|---|---|---|---|---|
| 3041462 | Benign | no assertion criteria provided | 0 | DDX54-related disorder; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Acute myeloid leukemia; Uveal melanoma; Colorectal cancer; Malignant tumor of esophagus | germline | 2 | Nov 04, 2019 | clinvar |