MSH6 NM_000179.2(MSH6):c.3738_3759inv (p.His1248_Ser1251delinsAsnGluTrpTer) — variant · CancerIndex

Variant · Structural

MSH6 NM_000179.2(MSH6):c.3738_3759inv (p.His1248_Ser1251delinsAsnGluTrpTer)

CI-VAR-00073146Explore in graph →p.His1248_Ser1251delinsAsnGluTrpTerNM_000179.2:c.3738_3759invClinVar 455281

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
455281	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary nonpolyposis colorectal neoplasms; Familial cancer of breast	germline	2	Oct 31, 2023	clinvar