RYR1 NM_000540.3(RYR1):c.11183T>C (p.Ile3728Thr)

CI-VAR-00209428Explore in graph →p.Ile3728ThrNM_000540.3:c.11183T>CClinVar 1444628 rs757580935

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
1444628	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	RYR1-related disorder; Inborn genetic diseases; Congenital multicore myopathy with external ophthalmoplegia; Malignant hyperthermia, susceptibility to, 1; Congenital myopathy with fiber type disproportion; Central core myopathy; Myopathy, RYR1-associated	germline	6	Sep 22, 2025	clinvar