SDHB NM_003000.3(SDHB):c.640C>T (p.Gln214Ter)

CI-VAR-00037799Explore in graph →p.Gln214TerNM_003000.3:c.640C>TClinVar 230243 rs876658461

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
230243	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Pheochromocytoma/paraganglioma syndrome 4; Gastrointestinal stromal tumor; Pheochromocytoma; Carney-Stratakis syndrome; Hereditary pheochromocytoma and paraganglioma	germline	14	May 15, 2026	clinvar