MSH3 NM_002439.5(MSH3):c.783_785dup (p.Glu261_Asp262insGlu) — variant · CancerIndex

Variant · Insertion

MSH3 NM_002439.5(MSH3):c.783_785dup (p.Glu261_Asp262insGlu)

CI-VAR-00297980Explore in graph →p.Glu261_Asp262insGluNM_002439.5:c.783_785dupClinVar 2451047 rs2546721283

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
2451047	Uncertain significance	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Dec 07, 2022	clinvar