Variant · Snv
ERBB2 E401G
CI-VAR-00000733Explore in graph →CIViC 4589
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
- 34997908
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Neoplasm of Unknown Primary1 | ||||||||
| ERBB2 E401G | (oncogenic) | Oncogenic | D | Supports Oncogenicity | 2 | submitted | EID11580H460 cells expressing the variant were tested to evaluate phosphorylation of the downstream signalling pathway. Results show an elevation in ERK phosphorylation similar to the positive control (S310F)… (full text at CIViC) PMID 34997908 · Harada et al., 2022 · Open in CIViC | civic |
| Unmapped disease1unmapped disease | ||||||||
| ERBB2 E401G | (functional) | Functional | D | Supports Gain Of Function | 2 | submitted | EID11579The variant did not show the formation of disulfide-linked dimers in NTH3T3 cells compared to WT with similar results as the positive control (S310F) (Figure. 2a) . Also, the variant increased phospho… (full text at CIViC) | |
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