MSH3 NM_002439.5(MSH3):c.708_711del (p.Gln235_Tyr236insTer) — variant · CancerIndex

Variant · Deletion

MSH3 NM_002439.5(MSH3):c.708_711del (p.Gln235_Tyr236insTer)

CI-VAR-00308467Explore in graph →p.Gln235_Tyr236insTerNM_002439.5:c.708_711delClinVar 2673564 rs2546721164

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
2673564	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Familial adenomatous polyposis 4; Hereditary cancer-predisposing syndrome	germline	2	Sep 29, 2025	clinvar