Variant · Snv
CEP89 NM_032816.5(CEP89):c.2120C>T (p.Ala707Val)
CI-VAR-00223020Explore in graph →p.Ala707ValNM_032816.5:c.2120C>TClinVar 1380861 rs145013119
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 |
|---|---|---|---|---|---|---|---|---|
| 1380861 | Uncertain significance | criteria provided, single submitter | 1 | Hepatocellular carcinoma; Malignant tumor of esophagus; Colon adenocarcinoma | germline | 2 | Nov 06, 2025 | clinvar |