Variant · Snv
DNAH7 NM_018897.3(DNAH7):c.1139T>G (p.Met380Arg)
CI-VAR-00058610Explore in graph →p.Met380ArgNM_018897.3:c.1139T>GClinVar 402759 rs144390858
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 |
|---|---|---|---|---|---|---|---|---|
| 402759 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | DNAH7-related disorder; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Gastric cancer; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Melanoma | germline | 7 | Jun 01, 2026 | clinvar |