Variant · Snv
CDH1 NM_004360.5(CDH1):c.1225T>C (p.Trp409Arg)
CI-VAR-00021040Explore in graph →p.Trp409ArgNM_004360.5:c.1225T>CClinVar 133855 rs587778176
Curated evidence
Evidence by cancer (0 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.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- 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 |
|---|---|---|---|---|---|---|---|---|
| 133855 | Likely benign | reviewed by expert panel | 3 | Hereditary cancer-predisposing syndrome; Hereditary diffuse gastric adenocarcinoma; Malignant tumor of breast; Breast and/or ovarian cancer; CDH1-related diffuse gastric and lobular breast cancer syndrome; CDH1-related disorder | germline | 13 | Aug 17, 2023 | clinvar |