SDHD NM_003002.4(SDHD):c.204C>T (p.Ser68=)

CI-VAR-00008570Explore in graph →p.Ser68=NM_003002.4:c.204C>TClinVar 44650 rs9919552

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
44650	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Pheochromocytoma; Mitochondrial complex 2 deficiency, nuclear type 3; Pheochromocytoma/paraganglioma syndrome 1; Carney-Stratakis syndrome; Cowden syndrome 3; Paragangliomas with sensorineural hearing loss; Pheochromocytoma/paraganglioma syndrome 3; Hereditary pheochromocytoma and paraganglioma; Cholangiocarcinoma; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Sarcoma; Melanoma	germline	23	Feb 04, 2026	clinvar