BRIP1 NM_032043.3(BRIP1):c.1203_1204del (p.Ala402fs)

CI-VAR-00252780Explore in graph →p.Ala402fsNM_032043.3:c.1203_1204delClinVar 1748000 rs730881647

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
1748000	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Familial cancer of breast; Fanconi anemia complementation group J	germline	4	Jan 22, 2026	clinvar