ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-0025	EPHA2	SNP	Missense_Mutation	1	16474993	C	A	19	64
ESO	ESO-187	EPHA2	SNP	Missense_Mutation	1	16475287	G	A	38	68
ESO	ESO-610	EPHA2	SNP	Nonsense_Mutation	1	16475530	G	A	46	96
HNSC	HN_0-064	EPHA2	SNP	Nonsense	1	16461597	G	A	47	69
HNSC	HN_62237	EPHA2	SNP	Nonsense	1	16459759	G	A	38	53
HNSC	HN_62421	EPHA2	SNP	Missense	1	16459741	C	T	31	98
LUAD	LUAD-B01246	EPHA2	SNP	Missense_Mutation	1	16464856	A	C	7	73
LUAD	LUAD-D02326	EPHA2	SNP	Missense_Mutation	1	16475256	G	A	43	95
LUAD	LUAD-F00170	EPHA2	SNP	Missense_Mutation	1	16461027	C	T	23	72
LUAD	LUAD-F00282	EPHA2	DNP	Missense_Mutation	1	16475077	CC	AA	22	48
LUAD	LUAD-RT-S01477	EPHA2	SNP	Missense_Mutation	1	16464866	C	T	29	65
LUAD	LUAD-S01315	EPHA2	SNP	Missense_Mutation	1	16456862	G	A	43	99
LUAD	LUAD_E00522	EPHA2	SNP	Missense_Mutation	1	16464913	C	G	30	95
MEL	ME020	EPHA2	SNP	Missense_Mutation	1	16475298	T	C	60	66
MEL	MEL-JWCI-WGS-1	EPHA2	SNP	Missense_Mutation	1	16451796	C	T	18	83
MEL	MEL-JWCI-WGS-1	EPHA2	SNP	Missense_Mutation	1	16456881	G	T	43	99
MEL	MEL-JWCI-WGS-1	EPHA2	SNP	Silent	1	16462261	G	A	43	58
MEL	MEL-JWCI-WGS-34	EPHA2	SNP	Missense_Mutation	1	16461053	C	T	30	62
MEL	MEL-JWCI-WGS-34	EPHA2	SNP	Splice_site	1	16461061	G	A	43	51
MEL	MEL-Ma-Mel-119	EPHA2	SNP	Missense_Mutation	1	16464548	G	A	43	84
MEL	MEL-Ma-Mel-35	EPHA2	SNP	Silent	1	16458879	G	A	41	60
MEL	MEL-Ma-Mel-53	EPHA2	SNP	Silent	1	16456798	G	A	37	50
LUAD	TCGA-05-4397	EPHA2	SNP	Missense_Mutation	1	16462249	C	A	26	47
LUAD	TCGA-05-4420	EPHA2	SNP	Silent	1	16464843	C	T	24	61
LUSC	TCGA-18-3409	EPHA2	SNP	Missense_Mutation	1	16456870	C	T	21	100
LUSC	TCGA-18-3411	EPHA2	SNP	Missense_Mutation	1	16458597	C	T	19	99
LUSC	TCGA-22-5472	EPHA2	SNP	Silent	1	16456843	G	T	45	49
OV	TCGA-24-1103	EPHA2	SNP	Missense_Mutation	1	16456018	C	G	26	99
OV	TCGA-24-1419	EPHA2	SNP	Missense_Mutation	1	16451772	G	A	38	78
LUAD	TCGA-38-4631	EPHA2	SNP	Missense_Mutation	1	16464386	C	A	27	67
KIRC	TCGA-A3-3367	EPHA2	SNP	Silent	1	16458586	G	A	40	43
UCEC	TCGA-A5-A0GI	EPHA2	SNP	Missense_Mutation	1	16464530	C	A	22	56
CRC	TCGA-A6-2672	EPHA2	SNP	Silent	1	16462195	C	T	27	46
CRC	TCGA-AA-3715	EPHA2	SNP	Missense_Mutation	1	16459788	G	A	40	98
CRC	TCGA-AA-3821	EPHA2	DEL	Frame_Shift_Del	1	16462199	G	-	39	45
CRC	TCGA-AA-3952	EPHA2	SNP	Silent	1	16477403	C	T	19	27
CRC	TCGA-AA-3966	EPHA2	DEL	Frame_Shift_Del	1	16474977	C	-	18	58
CRC	TCGA-AA-A00A	EPHA2	SNP	Missense_Mutation	1	16461660	G	A	38	91
CRC	TCGA-AA-A00J	EPHA2	SNP	Missense_Mutation	1	16475292	T	A	55	72
AML	TCGA-AB-2845	EPHA2	SNP	Missense_Mutation	1	16475259	G	A	38	95
UCEC	TCGA-AP-A051	EPHA2	SNP	Missense_Mutation	1	16460967	G	A	39	63
UCEC	TCGA-AP-A056	EPHA2	SNP	Missense_Mutation	1	16475362	C	T	27	69
UCEC	TCGA-AP-A0LM	EPHA2	SNP	Silent	1	16459817	C	A	30	53
UCEC	TCGA-AP-A0LM	EPHA2	SNP	Missense_Mutation	1	16460390	C	T	27	75
UCEC	TCGA-AX-A0J1	EPHA2	SNP	Silent	1	16459688	G	A	38	45
UCEC	TCGA-AX-A0J1	EPHA2	SNP	Splice_Site	1	16464769	C	T	19	95
UCEC	TCGA-B5-A0K6	EPHA2	SNP	Silent	1	16464460	G	A	38	45
HNSC	TCGA-BA-4077	EPHA2	SNP	Missense_Mutation	1	16458218	C	T	31	98
HNSC	TCGA-BA-5152	EPHA2	SNP	Splice_site	1	16461683	C	G	30	59
HNSC	TCGA-BA-5152	EPHA2	SNP	Nonsense_Mutation	1	16464404	G	C	45	95
HNSC	TCGA-BA-5152	EPHA2	SNP	Missense_Mutation	1	16475323	C	T	31	96
HNSC	TCGA-BA-6873	EPHA2	SNP	Nonsense_Mutation	1	16462185	G	A	39	92
BRCA	TCGA-BH-A0AV	EPHA2	SNP	Missense_Mutation	1	16475071	C	T	26	94
BLCA	TCGA-BT-A2LB	EPHA2	SNP	Missense_Mutation	1	16464519	C	T	26	57
BRCA	TCGA-C8-A1HL	EPHA2	SNP	Silent	1	16458583	G	A	44	80
HNSC	TCGA-CN-4726	EPHA2	INS	Frame_Shift_Ins	1	16461022	-	A	21	51
HNSC	TCGA-CN-4734	EPHA2	SNP	Nonsense_Mutation	1	16464404	G	C	45	95
HNSC	TCGA-CN-5355	EPHA2	SNP	Splice_site	1	16475542	A	C	6	88
HNSC	TCGA-CQ-5327	EPHA2	DEL	Frame_Shift_Del	1	16475129	CA	-	21	59
HNSC	TCGA-CQ-5334	EPHA2	SNP	Splice_Site	1	16464347	C	A	18	74
HNSC	TCGA-CV-7104	EPHA2	INS	Frame_Shift_Ins	1	16475417	-	CGCT	14	49
HNSC	TCGA-CV-7252	EPHA2	SNP	Nonsense_Mutation	1	16456829	C	T	21	99
HNSC	TCGA-CV-7252	EPHA2	INS	Frame_Shift_Ins	1	16475160	-	A	57	87
HNSC	TCGA-CV-7425	EPHA2	INS	Frame_Shift_Ins	1	16464477	-	G	59	65
HNSC	TCGA-CV-7438	EPHA2	DEL	In_Frame_Del	1	16475205	TTCAGC	-	60	87
HNSC	TCGA-CV-7440	EPHA2	SNP	Splice_Site	1	16477390	C	G	18	90
BLCA	TCGA-DK-A1A7	EPHA2	SNP	Missense_Mutation	1	16477395	T	C	64	65
BLCA	TCGA-DK-A2I6	EPHA2	SNP	Missense_Mutation	1	16475491	C	A	19	96
BRCA	TCGA-E2-A15A	EPHA2	SNP	Missense_Mutation	1	16464453	C	T	30	80
BRCA	TCGA-E9-A229	EPHA2	SNP	Missense_Mutation	1	16475203	C	T	19	61
BLCA	TCGA-FD-A3N5	EPHA2	SNP	Missense_Mutation	1	16456035	G	T	39	70
BLCA	TCGA-GV-A3QH	EPHA2	SNP	Missense_Mutation	1	16464437	T	C	57	87
BLCA	TCGA-H4-A2HQ	EPHA2	SNP	Nonsense_Mutation	1	16459810	C	A	30	98