FANCC NM_000136.3(FANCC):c.934A>G (p.Ile312Val)

CI-VAR-00019696Explore in graph →p.Ile312ValNM_000136.3:c.934A>GClinVar 127548 rs1800366

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
127548	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Fanconi anemia; Hereditary cancer-predisposing syndrome; Fanconi anemia complementation group C; Hereditary cancer; FANCC-related disorder	germline	16	Feb 04, 2026	clinvar