SMARCE1 NM_003079.5(SMARCE1):c.1234_1235insTTT (p.*412Pheext*1) — variant · CancerIndex

Variant · Insertion

SMARCE1 NM_003079.5(SMARCE1):c.1234_1235insTTT (p.412Pheext1)

CI-VAR-00209307Explore in graph →p.*412Pheext*1NM_003079.5:c.1234_1235insTTTClinVar 1361349 rs2143980165

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
1361349	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Familial meningioma; Hereditary cancer-predisposing syndrome	germline	2	Aug 18, 2025	clinvar