Variant · Snv
EIF2AK1 NM_014413.4(EIF2AK1):c.1673A>G (p.Lys558Arg)
CI-VAR-00283624Explore in graph →p.Lys558ArgNM_014413.4:c.1673A>GClinVar 2027206 rs2640
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 |
|---|---|---|---|---|---|---|---|---|
| 2027206 | Benign | criteria provided, single submitter | 1 | Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Thymoma; Uveal melanoma; Colorectal cancer; Cholangiocarcinoma | germline | 2 | Feb 01, 2026 | clinvar |