CDH1 NM_004360.5(CDH1):c.1013T>G (p.Phe338Cys)

CI-VAR-00064537Explore in graph →p.Phe338CysNM_004360.5:c.1013T>GClinVar 406621 rs1060501219

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
406621	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Familial cancer of breast; Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-predisposing syndrome	germline	3	May 05, 2026	clinvar