BRCA2 NM_000059.3(BRCA2):c.2077_2083delinsAACAGTT (p.Cys693_Lys695delinsAsnSerTer) — variant · CancerIndex

Variant · Indel

BRCA2 NM_000059.3(BRCA2):c.2077_2083delinsAACAGTT (p.Cys693_Lys695delinsAsnSerTer)

CI-VAR-00110383Explore in graph →p.Cys693_Lys695delinsAsnSerTerNM_000059.3:c.2077_2083delinsAACAGTTClinVar 626897 rs1566226077

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
626897	Uncertain significance	criteria provided, single submitter	1	Breast and/or ovarian cancer	germline	1	Feb 10, 2017	clinvar