FANCG NM_004629.2(FANCG):c.1189T>C (p.Phe397Leu)

CI-VAR-00061658Explore in graph →p.Phe397LeuNM_004629.2:c.1189T>CClinVar 408139 rs1060501868

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
408139	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Fanconi anemia; Fanconi anemia complementation group G; Inborn genetic diseases	germline	3	Jan 08, 2025	clinvar