TGFBR2 NM_003242.6(TGFBR2):c.76C>T (p.Pro26Ser)

CI-VAR-00145275Explore in graph →p.Pro26SerNM_003242.6:c.76C>TClinVar 858705 rs764160271

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
858705	Uncertain significance/Uncertain risk allele	criteria provided, multiple submitters, no conflicts	2	Familial thoracic aortic aneurysm and aortic dissection; Loeys-Dietz syndrome 2; Malignant tumor of esophagus; Colorectal cancer, hereditary nonpolyposis, type 6; Diabetic retinopathy	germline	7	Aug 19, 2025	clinvar