TBC1D24 NM_001199107.2(TBC1D24):c.1509C>T (p.Ser503=)

CI-VAR-00020496Explore in graph →p.Ser503=NM_001199107.2:c.1509C>TClinVar 130538 rs189089167

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
130538	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Familial infantile myoclonic epilepsy; Inborn genetic diseases; Malignant tumor of urinary bladder; Autosomal dominant nonsyndromic hearing loss 65; Developmental and epileptic encephalopathy, 1	germline	15	Feb 03, 2026	clinvar