Variant · Snv
CBFA2T2 NM_001032999.3(CBFA2T2):c.1466A>G (p.Asn489Ser)
CI-VAR-00338567Explore in graph →p.Asn489SerNM_001032999.3:c.1466A>GClinVar 3024887 rs75180889
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 |
|---|---|---|---|---|---|---|---|---|
| 3024887 | Likely benign | criteria provided, single submitter | 1 | Gastric cancer; Melanoma; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Uveal melanoma; Colorectal cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Familial cancer of breast | germline | 2 | Jun 01, 2025 | clinvar |