BRCA1 D1692N

CI-VAR-00000429Explore in graph →NP_009225.1:p.Asp1692AsnNM_007294.3:c.5074G>AClinVar 37632 CIViC 1244 rs80187739

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
37632	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Breast-ovarian cancer, familial, susceptibility to, 1; Hereditary cancer-predisposing syndrome; Hereditary breast ovarian cancer syndrome; Malignant tumor of urinary bladder	germline/somatic	16	Oct 26, 2025	clinvar