MSH6 NM_000179.3(MSH6):c.1050C>T (p.Ala350=)

CI-VAR-00026061Explore in graph →p.Ala350=NM_000179.3:c.1050C>TClinVar 182643 rs730881802

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
182643	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Hereditary cancer-predisposing syndrome; Lynch syndrome 5; Hereditary nonpolyposis colorectal neoplasms; Malignant tumor of breast; Breast and/or ovarian cancer; Lynch syndrome	germline	21	Feb 04, 2026	clinvar