FLCN NM_144997.7(FLCN):c.1337G>A (p.Arg446His)

CI-VAR-00119640Explore in graph →p.Arg446HisNM_144997.7:c.1337G>AClinVar 653565 rs750104212

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
653565	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Birt-Hogg-Dube syndrome; Hereditary cancer-predisposing syndrome; Colorectal cancer; Familial spontaneous pneumothorax; 17p11.2 microduplication syndrome; Nonpapillary renal cell carcinoma	germline	4	Feb 03, 2026	clinvar