Neoplasm by Site — Genomics

Neoplasm by Site — Genomics · CancerIndex

Genomics

Gene alteration frequencies by cohort

477 cohorts 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.

Refractory Cancers (RC) - Peripheral T-Cell Lymphoma (PTCL) RC-PTCLRC

58 cases with simple somatic mutation data · 58 cases total · Data Release 46.0 · mapped to Peripheral T-Cell Lymphoma, Not Otherwise Specified ONTOLOGY_EXACT

gdcObserved30 genes · frequency = affected / profiled, as published by the cohort.

#	Gene	Alteration	Affected (n)	Profiled (n)	Frequency (%)

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.

1	PRSS1	Ssm	42	58	72.4%	gdc
2	PRSS2	Ssm	41	58	70.7%	gdc
3	MTRNR2L6	Ssm	38	58	65.5%	gdc
5	OR11H12	Ssm	20	58	34.5%	gdc
4	POTEM	Ssm	20	58	34.5%	gdc
7	C8orf33	Ssm	18	58	31%	gdc
6	TPTE	Ssm	18	58	31%	gdc
14	POTEH	Ssm	17	58	29.3%	gdc
12	POTEG	Ssm	17	58	29.3%	gdc
8	GIMAP2	Ssm	17	58	29.3%	gdc
11	GIMAP4	Ssm	17	58	29.3%	gdc
10	GIMAP7	Ssm	17	58	29.3%	gdc
9	ACTR3C	Ssm	17	58	29.3%	gdc
13	GIMAP6	Ssm	17	58	29.3%	gdc
29	AC135068.4	Ssm	16	58	27.6%	gdc
18	SPATA31A5	Ssm	16	58	27.6%	gdc
15	ZBED6CL	Ssm	16	58	27.6%	gdc
16	CNTNAP3C	Ssm	16	58	27.6%	gdc
30	REPIN1	Ssm	16	58	27.6%	gdc
19	RARRES2	Ssm	16	58	27.6%	gdc
22	DPP6	Ssm	16	58	27.6%	gdc
35	ZNF775	Ssm	16	58	27.6%	gdc
28	FAM86B2	Ssm	16	58	27.6%	gdc
36	FASTK	Ssm	16	58	27.6%	gdc
17	AL391987.1	Ssm	16	58	27.6%	gdc
31	AL391987.2	Ssm	16	58	27.6%	gdc
26	GIMAP8	Ssm	16	58	27.6%	gdc
24	POTEB3	Ssm	16	58	27.6%	gdc
20	AC073111.3	Ssm	16	58	27.6%	gdc
38	ASIC3	Ssm	16	58	27.6%	gdc