Variant · Snv
CFAP298 NM_021254.4(CFAP298):c.308-16C>G
CI-VAR-00230413Explore in graph →NM_021254.4:c.308-16C>GClinVar 1550691 rs140374402
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 |
|---|---|---|---|---|---|---|---|---|
| 1550691 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Ovarian serous cystadenocarcinoma; Lung cancer; Primary ciliary dyskinesia 26; Familial cancer of breast; Acute myeloid leukemia; Cervical cancer | germline | 4 | Feb 01, 2026 | clinvar |