SDHA NM_004168.4(SDHA):c.969C>T (p.Gly323=)

CI-VAR-00023071Explore in graph →p.Gly323=NM_004168.4:c.969C>TClinVar 141242 rs142849100

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
141242	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Hereditary cancer-predisposing syndrome; Pheochromocytoma/paraganglioma syndrome 5; Mitochondrial complex II deficiency, nuclear type 1; Hereditary pheochromocytoma and paraganglioma; Leigh syndrome; Gastric cancer; Ovarian serous cystadenocarcinoma	germline	18	Jun 01, 2026	clinvar