SDHC NM_003001.5(SDHC):c.43C>T (p.Arg15Ter)

CI-VAR-00008373Explore in graph →p.Arg15TerNM_003001.5:c.43C>TClinVar 41776 rs201286421

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
41776	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Pheochromocytoma/paraganglioma syndrome 3; Hereditary cancer-predisposing syndrome; Hereditary pheochromocytoma and paraganglioma; Gastrointestinal stromal tumor; Carney-Stratakis syndrome; SDHC-related disorder; Inherited phaeochromocytoma and paraganglioma excluding NF1	germline	20	Jan 17, 2026	clinvar