RYR1 NM_000540.3(RYR1):c.10459G>A (p.Gly3487Ser)

CI-VAR-00150960Explore in graph →p.Gly3487SerNM_000540.3:c.10459G>AClinVar 863673 rs371645169

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
863673	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	RYR1-related disorder; Congenital multicore myopathy with external ophthalmoplegia; King Denborough syndrome; Central core myopathy; Congenital myopathy with fiber type disproportion; Malignant hyperthermia, susceptibility to, 1; Inborn genetic diseases	germline	6	May 12, 2026	clinvar