FANCC NM_000136.3(FANCC):c.1355_1358delinsGCCA (p.His452_Leu453delinsArgHis) — variant · CancerIndex

Variant · Indel

FANCC NM_000136.3(FANCC):c.1355_1358delinsGCCA (p.His452_Leu453delinsArgHis)

CI-VAR-00067100Explore in graph →p.His452_Leu453delinsArgHisNM_000136.3:c.1355_1358delinsGCCAClinVar 419059 rs1064793615

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
419059	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Fanconi anemia complementation group C	germline	2	Jul 11, 2021	clinvar