RYR1 NM_000540.3(RYR1):c.10648C>T (p.Arg3550Trp)

CI-VAR-00049636Explore in graph →p.Arg3550TrpNM_000540.3:c.10648C>TClinVar 281479 rs536304635

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
281479	Likely pathogenic	reviewed by expert panel	3	Congenital multicore myopathy with external ophthalmoplegia; Malignant hyperthermia, susceptibility to, 1; Central core myopathy; RYR1-related disorder; Inborn genetic diseases; King Denborough syndrome; RYR1-related myopathy	germline	16	Apr 13, 2026	clinvar