FANCF NM_022725.4(FANCF):c.267_268del (p.Cys89_Asp90delinsTer) — variant · CancerIndex

Variant · Other

FANCF NM_022725.4(FANCF):c.267_268del (p.Cys89_Asp90delinsTer)

CI-VAR-00307307Explore in graph →p.Cys89_Asp90delinsTerNM_022725.4:c.267_268delClinVar 2675559 rs1565055497

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
2675559	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Fanconi anemia complementation group F; Fanconi anemia; FANCF-related disorder	germline	3	Aug 10, 2023	clinvar