TBC1D24 NM_001199107.2(TBC1D24):c.571T>C (p.Cys191Arg)

CI-VAR-00303629Explore in graph →p.Cys191ArgNM_001199107.2:c.571T>CClinVar 2584794 rs2505514774

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
2584794	Uncertain significance	criteria provided, single submitter	1	Developmental and epileptic encephalopathy, 16; Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome; Familial infantile myoclonic epilepsy; DOORS syndrome; Malignant migrating partial seizures of infancy	germline	2	—	clinvar