ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-MEX-192	IPO7	SNP	Missense_Mutation	11	9446513	T	G	61	65
CRC	CRC-0010	IPO7	SNP	Missense	11	9463705	G	T	41	99
ESO	ESO-189	IPO7	SNP	Missense_Mutation	11	9444656	T	C	54	91
HNSC	HN_62854	IPO7	SNP	Nonsense	11	9450635	C	T	29	89
LUAD	LUAD-F00257	IPO7	SNP	Missense_Mutation	11	9456526	C	T	17	87
LUAD	LUAD-RT-S01774	IPO7	SNP	Nonsense_Mutation	11	9450116	C	A	17	48
LUAD	LUAD-S01356	IPO7	SNP	Missense_Mutation	11	9451304	A	T	14	93
MEL	ME009	IPO7	SNP	Missense_Mutation	11	9430125	G	A	33	100
MEL	ME045	IPO7	SNP	Silent	11	9455287	C	T	32	56
MEL	ME049	IPO7	SNP	Missense_Mutation	11	9445348	C	T	30	100
MEL	MEL-Ma-Mel-119	IPO7	DNP	Missense_Mutation	11	9450711	CC	TT	26	100
NB	NB-0433	IPO7	SNP	Silent	11	9459435	A	G	15	66
LUAD	TCGA-05-4396	IPO7	SNP	Missense_Mutation	11	9442240	C	A	21	99
LUAD	TCGA-05-4396	IPO7	SNP	Nonsense_Mutation	11	9459748	G	T	39	83
LUAD	TCGA-05-4427	IPO7	SNP	Missense_Mutation	11	9466700	A	T	3	69
LUAD	TCGA-17-Z031	IPO7	SNP	Missense_Mutation	11	9435846	A	T	7	80
LUAD	TCGA-44-2655	IPO7	SNP	Missense_Mutation	11	9463643	A	G	4	90
LUAD	TCGA-44-6774	IPO7	SNP	Missense_Mutation	11	9438673	T	C	60	79
LUAD	TCGA-64-5778	IPO7	SNP	Missense_Mutation	11	9459724	C	T	26	97
LUAD	TCGA-91-6829	IPO7	SNP	Missense_Mutation	11	9455345	C	T	18	99
CRC	TCGA-AA-3518	IPO7	SNP	Silent	11	9457898	G	A	42	50
CRC	TCGA-AA-3977	IPO7	SNP	Missense_Mutation	11	9456557	G	T	45	68
CRC	TCGA-AA-A00N	IPO7	SNP	Nonsense_Mutation	11	9450680	G	T	33	100
CRC	TCGA-AA-A01G	IPO7	SNP	Missense_Mutation	11	9456484	T	C	51	92
CRC	TCGA-AA-A01R	IPO7	SNP	Missense_Mutation	11	9431628	T	A	52	70
AML	TCGA-AB-2820	IPO7	SNP	Missense_Mutation	11	9455150	G	A	44	100
AML	TCGA-AB-2828	IPO7	SNP	Missense_Mutation	11	9442196	A	T	4	78
CRC	TCGA-AG-A002	IPO7	SNP	Silent	11	9459657	A	G	10	54
UCEC	TCGA-AP-A059	IPO7	SNP	Missense_Mutation	11	9462065	C	A	28	100
KIRC	TCGA-B0-4841	IPO7	SNP	Missense_Mutation	11	9424852	A	C	9	69
KIRC	TCGA-B0-5109	IPO7	SNP	Missense_Mutation	11	9446754	G	A	37	100
KIRC	TCGA-B0-5691	IPO7	SNP	Missense_Mutation	11	9459375	G	A	48	98
UCEC	TCGA-B5-A0JY	IPO7	SNP	Silent	11	9455362	C	A	32	56
UCEC	TCGA-BG-A0MI	IPO7	SNP	Missense_Mutation	11	9457843	A	C	12	90
UCEC	TCGA-BS-A0UJ	IPO7	SNP	Silent	11	9457907	T	C	63	53
UCEC	TCGA-BS-A0UJ	IPO7	SNP	Missense_Mutation	11	9459506	T	C	60	77
UCEC	TCGA-BS-A0UV	IPO7	SNP	Splice_Site	11	9455267	G	T	33	99
BLCA	TCGA-BT-A20J	IPO7	SNP	Missense_Mutation	11	9450660	G	A	33	69
BLCA	TCGA-BT-A3PH	IPO7	SNP	Missense_Mutation	11	9455272	C	G	32	77
BLCA	TCGA-BT-A3PJ	IPO7	SNP	Missense_Mutation	11	9435902	G	A	45	68
HNSC	TCGA-CN-4734	IPO7	SNP	Missense_Mutation	11	9430055	G	C	45	100
HNSC	TCGA-CQ-5331	IPO7	SNP	Silent	11	9456494	C	T	30	48
HNSC	TCGA-CR-5250	IPO7	SNP	Missense_Mutation	11	9466668	G	C	41	100
HNSC	TCGA-CR-7372	IPO7	SNP	Missense_Mutation	11	9445348	C	A	30	100
HNSC	TCGA-CV-7245	IPO7	SNP	Silent	11	9466672	A	C	12	51
HNSC	TCGA-CV-7440	IPO7	SNP	Splice_site	11	9459832	G	A	39	95
HNSC	TCGA-CX-7219	IPO7	SNP	Silent	11	9435863	C	T	32	66
UCEC	TCGA-DI-A0WH	IPO7	SNP	Missense_Mutation	11	9406315	A	G	10	88
BLCA	TCGA-DK-A1AC	IPO7	SNP	Silent	11	9424908	G	C	45	55
UCEC	TCGA-E6-A1LZ	IPO7	SNP	Missense_Mutation	11	9451265	C	G	32	88
BLCA	TCGA-G2-A2EO	IPO7	SNP	Nonsense_Mutation	11	9435956	C	T	29	100
BLCA	TCGA-GV-A3QI	IPO7	SNP	Missense_Mutation	11	9450663	G	A	48	100