SDHAF2 NM_017841.4(SDHAF2):c.215_216del (p.Leu71_Tyr72insTer) — variant · CancerIndex

Variant · Deletion

SDHAF2 NM_017841.4(SDHAF2):c.215_216del (p.Leu71_Tyr72insTer)

CI-VAR-00366951Explore in graph →p.Leu71_Tyr72insTerNM_017841.4:c.215_216delClinVar 3646144

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
3646144	Pathogenic	criteria provided, single submitter	1	Hereditary pheochromocytoma and paraganglioma	germline	1	Mar 16, 2024	clinvar