Variant · Snv
COL11A1 NM_001854.4(COL11A1):c.4303-22T>G
CI-VAR-00197252Explore in graph →NM_001854.4:c.4303-22T>GClinVar 1183103 rs74108036
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 |
|---|---|---|---|---|---|---|---|---|
| 1183103 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Familial cancer of breast; Ovarian serous cystadenocarcinoma; Ovarian cancer; Clear cell carcinoma of kidney | germline | 3 | Aug 06, 2019 | clinvar |