SMAD4 NM_005359.6(SMAD4):c.1086T>C (p.Phe362=)

CI-VAR-00020546Explore in graph →p.Phe362=NM_005359.6:c.1086T>CClinVar 132693 rs1801250

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
132693	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome; Myhre syndrome; Familial thoracic aortic aneurysm and aortic dissection; Generalized juvenile polyposis/juvenile polyposis coli; Juvenile polyposis syndrome	germline	26	May 01, 2026	clinvar