FANCC NM_000136.3(FANCC):c.1282_1283delinsGC (p.Phe428Ala) — variant · CancerIndex

Variant · Indel

FANCC NM_000136.3(FANCC):c.1282_1283delinsGC (p.Phe428Ala)

CI-VAR-00137968Explore in graph →p.Phe428AlaNM_000136.3:c.1282_1283delinsGCClinVar 818788 rs1588047935

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
818788	Uncertain significance	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Nov 04, 2018	clinvar