Variant · Deletion
DNAAF3 NM_001256715.2(DNAAF3):c.1585del (p.Ala529fs)
CI-VAR-00113185Explore in graph →p.Ala529fsNM_001256715.2:c.1585delClinVar 632321 rs1371933770
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 632321 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Primary ciliary dyskinesia; DDX41-related hematologic malignancy predisposition syndrome | germline | 4 | Jun 09, 2025 | clinvar |