ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-0590	TGFBR2	SNP	Missense_Mutation	3	30713886	T	G	55	88
HNSC	HN_00338	TGFBR2	SNP	Missense	3	30732942	G	A	45	88
HNSC	HN_63058	TGFBR2	SNP	Missense	3	30713856	G	T	46	95
LUAD	LUAD-S01315	TGFBR2	DNP	Nonsense_Mutation	3	30733046	GG	TT	39	19
LUAD	LUAD-YINHD	TGFBR2	SNP	Missense_Mutation	3	30713906	G	T	41	83
MEL	MEL-JWCI-WGS-13	TGFBR2	SNP	Missense_Mutation	3	30713774	C	T	30	73
MEL	MEL-JWCI-WGS-34	TGFBR2	SNP	Missense_Mutation	3	30713217	C	T	32	80
MEL	MEL-JWCI-WGS-34	TGFBR2	SNP	Missense_Mutation	3	30713733	C	T	30	98
MEL	MEL-Ma-Mel-48	TGFBR2	SNP	Nonsense_Mutation	3	30648460	C	T	29	69
MM	MM-0546	TGFBR2	SNP	Silent	3	30713185	C	T	29	55
MM	MM-0547	TGFBR2	SNP	Nonsense_Mutation	3	30648460	C	T	29	69
GBM	TCGA-06-0649	TGFBR2	SNP	Missense_Mutation	3	30691812	A	T	3	47
GBM	TCGA-06-0875	TGFBR2	SNP	Missense_Mutation	3	30732972	C	T	32	100
OV	TCGA-13-0791	TGFBR2	SNP	Missense_Mutation	3	30729881	A	C	1	91
LUAD	TCGA-17-Z043	TGFBR2	SNP	Missense_Mutation	3	30686295	T	C	59	81
OV	TCGA-24-1556	TGFBR2	SNP	Missense_Mutation	3	30713461	G	C	34	64
LUSC	TCGA-43-5668	TGFBR2	SNP	Missense_Mutation	3	30713504	A	G	5	91
LUAD	TCGA-44-2668	TGFBR2	SNP	Missense_Mutation	3	30732969	C	T	23	100
LUSC	TCGA-51-4079	TGFBR2	SNP	Nonsense_Mutation	3	30713591	C	T	21	99
OV	TCGA-61-2009	TGFBR2	SNP	Missense_Mutation	3	30729915	G	A	39	87
LUSC	TCGA-63-6202	TGFBR2	SNP	Silent	3	30713392	A	G	7	34
LUSC	TCGA-66-2789	TGFBR2	SNP	Silent	3	30713401	G	A	46	85
LUSC	TCGA-66-2791	TGFBR2	SNP	Nonsense_Mutation	3	30713559	C	G	29	84
CRC	TCGA-A6-3808	TGFBR2	SNP	Missense_Mutation	3	30715664	C	T	30	100
CRC	TCGA-AA-3514	TGFBR2	SNP	Missense_Mutation	3	30715624	G	A	33	100
CRC	TCGA-AA-3558	TGFBR2	SNP	Silent	3	30732980	C	A	22	44
CRC	TCGA-AA-A010	TGFBR2	SNP	Silent	3	30686246	C	T	19	37
CRC	TCGA-AA-A010	TGFBR2	SNP	Nonsense_Mutation	3	30729968	C	T	27	73
CRC	TCGA-AA-A01R	TGFBR2	SNP	Missense_Mutation	3	30715678	G	A	37	100
CRC	TCGA-AA-A029	TGFBR2	SNP	Missense_Mutation	3	30732957	G	A	37	100
CRC	TCGA-AA-A03F	TGFBR2	SNP	Missense_Mutation	3	30713643	T	C	55	90
AML	TCGA-AB-2828	TGFBR2	SNP	Missense_Mutation	3	30729900	T	A	64	92
BRCA	TCGA-AN-A0G0	TGFBR2	SNP	Nonsense_Mutation	3	30732950	G	A	43	88
UCEC	TCGA-AP-A051	TGFBR2	SNP	Silent	3	30686366	C	A	24	37
UCEC	TCGA-AP-A059	TGFBR2	SNP	Silent	3	30713602	G	T	39	28
BRCA	TCGA-AR-A1AP	TGFBR2	SNP	Missense_Mutation	3	30729932	G	A	37	100
UCEC	TCGA-AX-A0J0	TGFBR2	SNP	Missense_Mutation	3	30691875	A	C	1	61
UCEC	TCGA-B5-A11H	TGFBR2	SNP	Missense_Mutation	3	30686373	T	C	55	81
UCEC	TCGA-B5-A11U	TGFBR2	SNP	Silent	3	30729913	G	A	46	71
UCEC	TCGA-BG-A0M0	TGFBR2	SNP	Missense_Mutation	3	30713742	G	A	39	98
BRCA	TCGA-BH-A0B5	TGFBR2	SNP	Missense_Mutation	3	30691805	G	A	45	73
KIRC	TCGA-BP-4169	TGFBR2	SNP	Missense_Mutation	3	30732950	G	T	43	88
UCEC	TCGA-BS-A0UF	TGFBR2	SNP	Missense_Mutation	3	30713506	G	T	33	86
UCEC	TCGA-BS-A0UJ	TGFBR2	SNP	Silent	3	30713624	T	C	60	51
HNSC	TCGA-CN-4731	TGFBR2	DEL	In_Frame_Del	3	30691918	TGA	-	55	25
HNSC	TCGA-CR-7376	TGFBR2	SNP	Nonsense_Mutation	3	30713559	C	G	29	84
HNSC	TCGA-CR-7402	TGFBR2	SNP	Missense_Mutation	3	30691784	A	G	2	84
HNSC	TCGA-CV-5444	TGFBR2	SNP	Splice_Site	3	30729875	G	A	33	99
HNSC	TCGA-CV-5444	TGFBR2	SNP	Missense_Mutation	3	30729917	G	A	41	87
HNSC	TCGA-CV-6936	TGFBR2	SNP	Silent	3	30713698	C	T	29	55
HNSC	TCGA-CV-6943	TGFBR2	SNP	Nonsense_Mutation	3	30691947	C	G	29	66
HNSC	TCGA-CV-6954	TGFBR2	SNP	Nonsense_Mutation	3	30732963	G	T	33	100
HNSC	TCGA-CV-6955	TGFBR2	SNP	Missense_Mutation	3	30715720	C	T	31	82
HNSC	TCGA-CV-6961	TGFBR2	SNP	Nonsense_Mutation	3	30691947	C	G	29	66
HNSC	TCGA-CV-7252	TGFBR2	SNP	Nonsense_Mutation	3	30713559	C	G	29	84
HNSC	TCGA-CV-7411	TGFBR2	SNP	Missense_Mutation	3	30715717	T	C	50	93
UCEC	TCGA-D1-A103	TGFBR2	SNP	Silent	3	30691813	G	A	34	46
UCEC	TCGA-D1-A16F	TGFBR2	SNP	Missense_Mutation	3	30713718	G	A	38	62
UCEC	TCGA-D1-A17Q	TGFBR2	SNP	Missense_Mutation	3	30715678	G	A	37	100
BRCA	TCGA-EW-A1IZ	TGFBR2	SNP	Silent	3	30713659	C	T	19	38
BLCA	TCGA-G2-A2ES	TGFBR2	INS	Frame_Shift_Ins	3	30713456	-	C	42	100
BLCA	TCGA-G2-A3IB	TGFBR2	SNP	Missense_Mutation	3	30715617	G	T	47	100
BLCA	TCGA-GC-A3I6	TGFBR2	SNP	Missense_Mutation	3	30713543	G	A	33	99
CARC	Carc-BWH17	TGFBR2	DEL	Frame_Shift_Del	3	30691872	A	-	9	84
CARC	Carc-DFCI-136	TGFBR2	SNP	Missense_Mutation	3	30729896	C	T	30	100