Variant · Snv
ERBB2 D769H
CI-VAR-00000532Explore in graph →NP_001276866.1:p.Asp769HisNM_001289937.1:c.2305G>CClinVar 375991 CIViC 35 rs121913468
Curated evidence
Evidence by cancer (3 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
- 25636205
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Bladder Carcinoma1 | ||||||||
| ERBB2 D769H | Chemotherapy | Predictive | C | Supports Sensitivity Response | 3 | submitted | EID11499Variant found in a patient that was diagnosed with muscle-invasive bladder cancer in pretreatment transurethral resection tumor samples (Fig. 1; Patients ID:CF3097). The patient was categorised as a “… (full text at CIViC) PMID 25636205 · Groenendijk et al., 2016 · Open in CIViC | civic |
| Malignant Breast Neoplasm1 | ||||||||
| ERBB2 D769H | Lapatinib + NeratinibSubstitutes | Predictive | D | Supports Sensitivity Response | 4 | accepted | EID279In MCF10A cell lines, the D769H mutation was shown to be sensitive to neratinib. PMID 23220880 · | |
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