Variant · Snv
EIF4A3 NM_014740.4(EIF4A3):c.867G>A (p.Lys289=)
CI-VAR-00127755Explore in graph →p.Lys289=NM_014740.4:c.867G>AClinVar 710510 rs35229151
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 710510 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Hepatocellular carcinoma; Cervical cancer; Colon adenocarcinoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Clear cell carcinoma of kidney; Acute myeloid leukemia; Lung cancer | germline | 3 | Nov 14, 2024 | clinvar |