Variant · Snv
EIF2B2 NM_014239.4(EIF2B2):c.434-35T>A
CI-VAR-00198966Explore in graph →NM_014239.4:c.434-35T>AClinVar 1229760 rs201252172
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 |
|---|---|---|---|---|---|---|---|---|
| 1229760 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Acute myeloid leukemia; Lung cancer; Sarcoma; Uterine carcinosarcoma | germline | 3 | May 12, 2021 | clinvar |