Pharyngeal Neoplasm — Genomics

Pharyngeal Neoplasm — 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.

Nasopharyngeal Carcinoma (Singapore, Nat Genet 2014) npc_nusingaporeSingapore

56 cases with simple somatic mutation data · 56 cases total · 2026-01-08 · mapped to Nasopharyngeal Carcinoma EXACT_IDENTIFIER

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

#	Gene	Alteration	Affected (n)	Profiled (n)	Frequency (%)	Source
1	TP53	Ssm	7	56	12.5%	cbioportal
2	TTN	Ssm	5	56	8.9%	cbioportal
4	SYNE1	Ssm	4	56	7.1%	cbioportal
3	MUC17	Ssm	4	56	7.1%	cbioportal
13	RYR2	Ssm	3	56	5.4%	cbioportal
11	KMT2D	Ssm	3	56	5.4%	cbioportal
15	TET2	Ssm	3	56	5.4%	cbioportal
17	ZNF462

Data updated 22 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.