MYL2 NM_000432.4(MYL2):c.401A>C (p.Glu134Ala)

CI-VAR-00008523Explore in graph →p.Glu134AlaNM_000432.4:c.401A>CClinVar 43475 rs143139258

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
43475	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Hypertrophic cardiomyopathy; Hypertrophic cardiomyopathy 10; Cardiovascular phenotype; Dilated cardiomyopathy 1S; Primary dilated cardiomyopathy; Cardiomyopathy; Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy; Sarcoma	germline	24	Jun 17, 2026	clinvar