Meningioma — Genomics

Meningioma — Genomics · CancerIndex

Genomics

Gene alteration frequencies by cohort

1 cohort mapped to this entity or its descendants. Each frequency is affected / profiled within one cohort; cohorts are shown separately because case selection, sequencing depth and definitions differ. By default the cohort with the most cases profiled is shown.

Meningioma (University of Toronto, Nature 2021) mng_utoronto_2021University of Toronto

115 cases with simple somatic mutation data · 121 cases total · 2026-01-08 · mapped to Meningioma EXACT_IDENTIFIER

cbioportalObserved30 genes · frequency = affected / profiled, as published by the cohort.

#	Gene	Alteration	Affected (n)	Profiled (n)	Frequency (%)	Source
1	NF2	Ssm	64	115	55.7%	cbioportal
2	TTN	Ssm	23	115	20%	cbioportal
3	OBSCN	Ssm	12	115	10.4%	cbioportal
4	FLG	Ssm	10	115	8.7%	cbioportal
5	TRAF7	Ssm	8	115	7%	cbioportal
6	PLEC	Ssm	7	115	6.1%	cbioportal
13	SALL3	Ssm	6	115	5.2%	cbioportal
14	SMARCB1

Data updated 21 days agoSource updated 2026-01-08

Cohorts mapped to a descendant (e.g. a subtype) are included because their cases belong to this entity by definition; the mapping and its match type are shown per cohort.