FANCC NM_000136.3(FANCC):c.12_14delinsAAGATCAA (p.Asp4fs) — variant · CancerIndex

Variant · Indel

FANCC NM_000136.3(FANCC):c.12_14delinsAAGATCAA (p.Asp4fs)

CI-VAR-00138028Explore in graph →p.Asp4fsNM_000136.3:c.12_14delinsAAGATCAAClinVar 818570 rs1588353886

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
818570	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Fanconi anemia complementation group C	germline	2	Jan 07, 2022	clinvar