BARD1 NM_000465.4(BARD1):c.1187_1196delinsTTG (p.Pro396fs) — variant · CancerIndex

Variant · Indel

BARD1 NM_000465.4(BARD1):c.1187_1196delinsTTG (p.Pro396fs)

CI-VAR-00167357Explore in graph →p.Pro396fsNM_000465.4:c.1187_1196delinsTTGClinVar 969189 rs1694949382

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
969189	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Familial cancer of breast; Hereditary cancer-predisposing syndrome	germline	3	Jun 28, 2025	clinvar