Variant · Snv
ERBB2 D769Y
CI-VAR-00000535Explore in graph →NP_004439.2:p.Asp769TyrNM_004448.3:c.2305G>TClinVar 375992 CIViC 36 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
- 35939768
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Extramammary Paget Disease1 | ||||||||
| ERBB2 D769Y | Afatinib | Predictive | C | Supports Sensitivity Response | 3 | accepted | EID11688In this phase II NCI-MATCH trial, a patient with extra-mammary Paget disease of the skin with ERBB2 D769Y mutation was treated with afatinib. A confirmed RECIST response was reported in the patient wh… (full text at CIViC) PMID 35939768 · Bedard et al., 2022 · Open in CIViC | civic |
| Malignant Breast Neoplasm1 | ||||||||
| ERBB2 D769Y | Neratinib | Predictive | D | Supports Sensitivity Response | 4 | accepted | EID280In MCF10A cell lines, the D769Y mutation was shown to be sensitive to neratinib. PMID 23220880 · Bose et al., 2013 · Open in 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