Variant · Snv
EIF4A2 NM_001967.4(EIF4A2):c.772-3C>T
CI-VAR-00339031Explore in graph →NM_001967.4:c.772-3C>TClinVar 3042089 rs75837460
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 |
|---|---|---|---|---|---|---|---|---|
| 3042089 | Benign | no assertion criteria provided | 0 | EIF4A2-related disorder; Nonpapillary renal cell carcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Lung cancer; Cervical cancer; Melanoma; Hepatocellular carcinoma; Ovarian cancer; Colorectal cancer; Sarcoma; Lymphoma; Ovarian serous cystadenocarcinoma; Malignant lymphoma, large B-cell, diffuse; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 2 | Nov 27, 2019 | clinvar |