Variant · Snv
DNAH11 NM_001277115.2(DNAH11):c.13163-19T>A
CI-VAR-00047269Explore in graph →NM_001277115.2:c.13163-19T>AClinVar 257869 rs72658832
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 |
|---|---|---|---|---|---|---|---|---|
| 257869 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Primary ciliary dyskinesia; Gastric cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uterine corpus endometrial carcinoma; Primary ciliary dyskinesia 7 | germline | 8 | Jan 30, 2026 | clinvar |