Variant · Snv
CFAP44 NM_001164496.2(CFAP44):c.4759-3C>T
CI-VAR-00200268Explore in graph →NM_001164496.2:c.4759-3C>TClinVar 1267032 rs2270784
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 |
|---|---|---|---|---|---|---|---|---|
| 1267032 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Cervical cancer; Ovarian cancer; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Familial pancreatic carcinoma; Sarcoma; Uterine carcinosarcoma; Lymphoma; Hepatocellular carcinoma | germline | 3 | Jun 25, 2020 | clinvar |