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Gene/Event	Cancer Type	Patient	Variant	Mutation Level
PTPRT	Breast Cancer	p123_case9	p.S220fs	Trunk mutation
PTPRT	Colorectal Cancer	p001_PCRC03	Chr20:41101033:G>T	Trunk mutation
PTPRT	Colorectal Cancer	p001_PCRC15	Chr20:41420087:G>T	Branch mutation
PTPRT	Colorectal Cancer	p034_MSU2	Chr20:40944608:G>A	Trunk mutation
PTPRT	Colorectal Cancer	p034_MSU3	Chr20:40827893:G>A	Trunk mutation
PTPRT	Colorectal Cancer	p040_case3	Chr20:41514506:A>-	Private mutation
PTPRT	Colorectal Cancer	p040_case4	Chr20:40911143:C>T	Branch mutation
PTPRT	Colorectal Cancer	p040_case9	Chr20:41419958:G>A	Trunk mutation
PTPRT	Colorectal Cancer	p069_p06	p.R1395H	Private mutation
PTPRT	Colorectal Cancer	p069_p15	p.A731T	Private mutation
PTPRT	Colorectal Cancer	p104_CD02	p.A487D	Private mutation
PTPRT	Colorectal Cancer	p155_p229	p.D534E	Private mutation
PTPRT	Colorectal Cancer	p155_p252	p.K1033T	Private mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p008_ESCC06	p.D824N	Trunk mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p008_ESCC09	p.G818W	Private mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p008_ESCC12	p.R546Q	Trunk mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p124_ESCC012	p.P291S	Private mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p124_ESCC043	p.G369S	Trunk mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p124_ESCC043	p.R1344W	Branch mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p128_P03	Chr20:41076863:C>T	Private mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p128_P14	Chr20:40748578:C>T	Private mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p128_SP10	Chr20:41419986:G>A	Trunk mutation
PTPRT	Esophageal Squamous Cell Carcinoma	p128_SP28	Chr20:40713335:G>T	Private mutation
PTPRT	Gastric Adenocarcinoma	p011_MSS1	p.A533S	Private mutation
PTPRT	Gastric Adenocarcinoma	p011_MSS3	p.P963P	Private mutation
PTPRT	Gastric Adenocarcinoma	p011_MSI-H1	p.T879M	Private mutation
PTPRT	Gastric Adenocarcinoma	p011_MSI-H2	p.D353D	Trunk mutation
PTPRT	Gastric Carcinoma	p106_GC01	p.Q749Q	Trunk mutation
PTPRT	Gastric Carcinoma	p106_GC04	p.Q1147K	Private mutation
PTPRT	Gastric Carcinoma	p106_GC07	p.R1403R	Private mutation
PTPRT	Gastric Carcinoma	p106_GC09	p.V846I	Trunk mutation
PTPRT	Gastric Carcinoma	p106_GC09	p.T1268T	Private mutation
PTPRT	Glioblastoma	p113_case07	p.T443I	Private mutation
PTPRT	Glioma	p168_P01	p.T53I	Private mutation
PTPRT	Glioma	p168_P18	p.Q880Q	Private mutation
PTPRT	Hepatocellular Carcinoma	p061_P01	Chr20:40743933:G>T	Trunk mutation
PTPRT	Acute Myeloid Leukemia	p114_AML01	p.P1232L	Trunk mutation
PTPRT	Lung Cancer	p021_L002	p.E667K	Branch mutation
PTPRT	Lung Cancer	p021_L003	intronic	Private mutation
PTPRT	Medulloblastoma	p072_MB5	Chr20:41100976:C>A	Trunk mutation
PTPRT	Medulloblastoma	p072_MB6	Chr20:40790081:A>G	Private mutation
PTPRT	Melanoma	p043_A	p.S778F	Trunk mutation
PTPRT	Melanoma	p043_A	p.M747I	Trunk mutation
PTPRT	Melanoma	p043_C	p.Q162*	Trunk mutation
PTPRT	Melanoma	p043_D	p.V30I	Trunk mutation
PTPRT	Melanoma	p043_F	p.M600I	Trunk mutation
PTPRT	Melanoma	p043_F	p.S647L	Trunk mutation
PTPRT	Melanoma	p043_G	p.R533H	Trunk mutation
PTPRT	Melanoma	p043_H	p.P485L	Trunk mutation
PTPRT	Melanoma	p135_p04	Chr20:40735551:C>A	Private mutation
PTPRT	Melanoma	p135_p10	Chr20:40790091:G>A	Trunk mutation
PTPRT	Melanoma	p135_p12	Chr20:41076878:C>T	Trunk mutation
PTPRT	Melanoma	p135_p12	Chr20:41306622:T>C	Trunk mutation
PTPRT	Melanoma	p135_p18	Chr20:40709519:C>T	Trunk mutation
PTPRT	Melanoma	p135_p20	Chr20:40743863:G>A	Trunk mutation
PTPRT	Melanoma	p135_p25	Chr20:40730801:C>T	Trunk mutation
PTPRT	Melanoma	p135_p25	Chr20:40770576:G>A	Trunk mutation
PTPRT	Melanoma	p135_p28	Chr20:40790171:GG>AA	Trunk mutation
PTPRT	Ovarian Cancer	p144_AOCS064	p.L838F	Private mutation
PTPRT	Ovarian Cancer	p153_RJOC01	p.Q207H	Trunk mutation
PTPRT	Clear Cell Renal Cell Carcinoma	p019_RMH002	Chr20:41419958:p.N>K	Branch mutation
PTPRT	Renal Cell Carcinoma	p073_RCC1	Chr20:40714388:G>A	Branch mutation
PTPRT	Urothelial Carcinoma	p142_p21	-	Private mutation
PTPRT	Urothelial Carcinoma	p142_p36	-	Private mutation
PTPRT	Urothelial Carcinoma	p142_p37	-	Private mutation

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