CFTR NM_000492.4(CFTR):c.3276C>A (p.Tyr1092Ter)

CI-VAR-00007837Explore in graph →p.Tyr1092TerNM_000492.4:c.3276C>AClinVar 38728 rs121908761

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
38728	Pathogenic	reviewed by expert panel	3	Cystic fibrosis; Hereditary pancreatitis; Congenital bilateral aplasia of vas deferens from CFTR mutation; Bronchiectasis with or without elevated sweat chloride 1; CFTR-related disorder; Melanoma-pancreatic cancer syndrome	germline	25	Mar 17, 2017	clinvar