NBN NM_002485.5(NBN):c.698_701del (p.Lys233fs)

CI-VAR-00020005Explore in graph →p.Lys233fsNM_002485.5:c.698_701delClinVar 127878 rs587780100

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
127878	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and immunodeficiency; Malignant tumor of breast; Acute lymphoid leukemia; Aplastic anemia; NBN-related disorder	germline	15	Jan 12, 2026	clinvar