NBN NM_002485.5(NBN):c.591_603delinsTTG (p.Pro198fs)

CI-VAR-00083671Explore in graph →p.Pro198fsNM_002485.5:c.591_603delinsTTGClinVar 481871 rs1554564297

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
481871	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Microcephaly, normal intelligence and immunodeficiency; Acute lymphoid leukemia; Aplastic anemia	germline	8	Jul 01, 2025	clinvar