NBN NM_002485.5(NBN):c.797C>T (p.Pro266Leu)

CI-VAR-00021386Explore in graph →p.Pro266LeuNM_002485.5:c.797C>TClinVar 134878 rs769420

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
134878	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and immunodeficiency; Hereditary breast ovarian cancer syndrome; Acute lymphoid leukemia; Aplastic anemia	germline	20	Jun 01, 2026	clinvar