MYH11 NM_002474.3(MYH11):c.935A>G (p.Asn312Ser)

CI-VAR-00106940Explore in graph →p.Asn312SerNM_002474.3:c.935A>GClinVar 566653 rs149964928

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
566653	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Aortic aneurysm, familial thoracic 4; Familial thoracic aortic aneurysm and aortic dissection; Visceral myopathy 2; Megacystis-microcolon-intestinal hypoperistalsis syndrome 2; Ovarian serous cystadenocarcinoma	germline	9	Dec 28, 2025	clinvar