RAD51B NM_001321821.2(RAD51B):c.1275_1276dup (p.Ter426CysextTer?) — variant · CancerIndex

Variant · Other

RAD51B NM_001321821.2(RAD51B):c.1275_1276dup (p.Ter426CysextTer?)

CI-VAR-00302120Explore in graph →p.Ter426CysextTer?NM_001321821.2:c.1275_1276dupClinVar 2577876 rs1410470158

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
2577876	Uncertain significance	criteria provided, single submitter	1	Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	germline	1	Aug 31, 2021	clinvar