CYP17A1 NM_000102.4(CYP17A1):c.715C>T (p.Arg239Ter)

CI-VAR-00005253Explore in graph →p.Arg239TerNM_000102.4:c.715C>TClinVar 1782 rs104894136

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
1782	Pathogenic	criteria provided, multiple submitters, no conflicts	2	17-alpha-hydroxylase/17,20-lyase deficiency, combined partial; Breast cancer, susceptibility to; Deficiency of steroid 17-alpha-monooxygenase	germline	6	May 23, 2026	clinvar