Variant · Snv
EGF NM_001963.6(EGF):c.2351A>T (p.Asp784Val)
CI-VAR-00051074Explore in graph →p.Asp784ValNM_001963.6:c.2351A>TClinVar 347246 rs11569017
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 |
|---|---|---|---|---|---|---|---|---|
| 347246 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Renal hypomagnesemia 4; Acute myeloid leukemia; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Nonpapillary renal cell carcinoma | germline | 6 | Feb 03, 2026 | clinvar |