NBN NM_002485.5(NBN):c.1234_1235del (p.Ser411_Asn412insTer) — variant · CancerIndex

Variant · Deletion

NBN NM_002485.5(NBN):c.1234_1235del (p.Ser411_Asn412insTer)

CI-VAR-00183353Explore in graph →p.Ser411_Asn412insTerNM_002485.5:c.1234_1235delClinVar 1075267 rs2129720196

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
1075267	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Microcephaly, normal intelligence and immunodeficiency; Hereditary cancer-predisposing syndrome; Aplastic anemia	germline	3	Feb 13, 2023	clinvar