Variant · Snv
EGFR G63R
CI-VAR-00001778Explore in graph →NP_005219.2:p.Gly63ArgNM_005228.5:c.187G>ACIViC 3488
Curated evidence
Evidence by cancer (2 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.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 31290142
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Neoplasm1 | ||||||||
| EGFR G63R | (oncogenic) | Oncogenic | D | Supports Oncogenicity | 3 | submitted | EID9645The oncogenic potential of somatic EGFR mutations found in colorectal cancer samples were tested. IL-3 independent growth of Ba/F3 cells was achieved when cells were transduced with EGFR G63R. NIH-3T3… (full text at CIViC) PMID 31290142 · Kim et al., 2020 · Open in CIViC | civic |
| Unmapped disease1unmapped disease | ||||||||
| EGFR G63R | (functional) | Functional | D | Supports Gain Of Function | 3 | submitted | EID9637Ba/F3 cells transfected with EGFR G63R had levels of p-EGFR, p-STAT5, and p-AKT that were similar to known activating mutation L858R and higher than in cells expressing wild-type EGFR. PMID 31290142 · Kim et al., 2020 · | |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available