CTNNA1 NM_001903.5(CTNNA1):c.1337_1338insACCT (p.Val447fs) — variant · CancerIndex

Variant · Insertion

CTNNA1 NM_001903.5(CTNNA1):c.1337_1338insACCT (p.Val447fs)

CI-VAR-00368198Explore in graph →p.Val447fsNM_001903.5:c.1337_1338insACCTClinVar 3653855

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
3653855	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome	germline	2	Jul 15, 2025	clinvar