SMARCE1 NM_003079.5(SMARCE1):c.1086_1087delinsAT (p.Thr363Ser) — variant · CancerIndex

Variant · Indel

SMARCE1 NM_003079.5(SMARCE1):c.1086_1087delinsAT (p.Thr363Ser)

CI-VAR-00161678Explore in graph →p.Thr363SerNM_003079.5:c.1086_1087delinsATClinVar 951720 rs2037062544

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
951720	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Familial meningioma; Hereditary cancer-predisposing syndrome	germline	2	Jul 24, 2024	clinvar