Variant · Snv
EGFR G724S
CI-VAR-00001800Explore in graph →NP_005219.2:p.Gly724SerNM_005228.4:c.2170G>AClinVar 376360 CIViC 317 rs1051753269
Curated evidence
Evidence by cancer (4 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
- 24894453
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Colorectal Neoplasm1 | ||||||||
| EGFR G724S | Cetuximab | Predictive | D | Supports Sensitivity Response | 4 | accepted | EID786Whole genome sequencing of a case of colon carcinoma revealed a G724S mutation in the EGFR gene. In-vitro, this mutation was shown to be oncogenic and sensitive to Cetuximab, yet relatively insensitiv… (full text at CIViC) PMID 24894453 · Cho et al., 2014 · Open in CIViC | civic |
| Malignant Neoplasm1 | ||||||||
| EGFR G724S | (oncogenic) | Oncogenic | D | Supports Oncogenicity | 3 | submitted | EID9652The 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 G724S. NIH-3T… (full text at CIViC) PMID 31290142 · | |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- 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 |
|---|---|---|---|---|---|---|---|---|
| 376360 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | EGFR-related lung cancer; Hereditary cancer-predisposing syndrome; Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype | germline/somatic | 4 | Jan 14, 2026 | clinvar |