Variant · Snv
ODAD1 NM_001364171.2(ODAD1):c.1071G>A (p.Glu357=)
CI-VAR-00047829Explore in graph →p.Glu357=NM_001364171.2:c.1071G>AClinVar 262509 rs79967289
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 |
|---|---|---|---|---|---|---|---|---|
| 262509 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Primary ciliary dyskinesia; Primary ciliary dyskinesia 20; Ovarian serous cystadenocarcinoma; Lung cancer; Gastric cancer; Uterine carcinosarcoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney | germline | 7 | Jan 26, 2026 | clinvar |