FLCN NM_144997.7(FLCN):c.669_671delinsGCACAGCGTGCTCAG (p.Asn223_Thr224delinsLysHisSerValLeuArg) — variant · CancerIndex

Variant · Indel

FLCN NM_144997.7(FLCN):c.669_671delinsGCACAGCGTGCTCAG (p.Asn223_Thr224delinsLysHisSerValLeuArg)

CI-VAR-00141499Explore in graph →p.Asn223_Thr224delinsLysHisSerValLeuArgNM_144997.7:c.669_671delinsGCACAGCGTGCTCAGClinVar 826553 rs1597602427

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
826553	Uncertain significance	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Sep 27, 2019	clinvar