FLCN NM_144997.7(FLCN):c.1145_1147dup (p.Asp382_Leu383insHis) — variant · CancerIndex

Variant · Insertion

FLCN NM_144997.7(FLCN):c.1145_1147dup (p.Asp382_Leu383insHis)

CI-VAR-00315044Explore in graph →p.Asp382_Leu383insHisNM_144997.7:c.1145_1147dupClinVar 2738165 rs1330807456

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
2738165	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Birt-Hogg-Dube syndrome; Hereditary cancer-predisposing syndrome	germline	2	Jan 25, 2026	clinvar