ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-LS4616	GNPTAB	SNP	Missense_Mutation	12	102154918	G	A	39	98
ESO	ESO-0079	GNPTAB	SNP	Silent	12	102164241	C	A	26	49
LUAD	LUAD-F00170	GNPTAB	SNP	Missense_Mutation	12	102224401	T	C	49	65
LUAD	LUAD-RT-S01774	GNPTAB	SNP	Missense_Mutation	12	102158320	G	A	46	51
LUAD	LUAD-S00488	GNPTAB	SNP	Missense_Mutation	12	102158249	A	T	4	54
MEL	ME009	GNPTAB	SNP	Missense_Mutation	12	102158288	C	T	22	45
MEL	MEL-Ma-Mel-122	GNPTAB	SNP	Missense_Mutation	12	102153873	G	A	41	98
LUAD	TCGA-17-Z053	GNPTAB	SNP	Nonsense_Mutation	12	102153823	G	C	36	55
LUSC	TCGA-22-4593	GNPTAB	SNP	Silent	12	102155097	T	C	51	45
LUSC	TCGA-22-5489	GNPTAB	SNP	Splice_Site	12	102161813	A	G	14	77
OV	TCGA-24-1616	GNPTAB	SNP	Nonsense_Mutation	12	102153834	G	A	45	98
OV	TCGA-24-2298	GNPTAB	SNP	Missense	12	102155355	C	T	32	99
LUSC	TCGA-33-4547	GNPTAB	SNP	Nonsense_Mutation	12	102158641	G	C	45	64
LUAD	TCGA-35-5375	GNPTAB	SNP	Silent	12	102160038	A	C	6	32
LUAD	TCGA-44-4112	GNPTAB	SNP	Silent	12	102179940	G	A	35	68
LUAD	TCGA-50-5066	GNPTAB	SNP	Missense_Mutation	12	102164889	T	A	60	63
LUSC	TCGA-60-2698	GNPTAB	SNP	Missense_Mutation	12	102158651	C	A	29	51
LUAD	TCGA-64-1678	GNPTAB	SNP	Missense_Mutation	12	102183810	C	T	19	99
BRCA	TCGA-A1-A0SJ	GNPTAB	SNP	Missense_Mutation	12	102161847	G	A	45	85
BRCA	TCGA-A2-A04W	GNPTAB	SNP	Nonsense_Mutation	12	102158936	G	A	37	77
UCEC	TCGA-A5-A0GP	GNPTAB	SNP	Missense_Mutation	12	102151060	C	T	27	100
BRCA	TCGA-A8-A06Z	GNPTAB	SNP	Missense_Mutation	12	102179874	A	G	9	50
BRCA	TCGA-A8-A076	GNPTAB	SNP	Missense_Mutation	12	102159934	T	C	50	89
BRCA	TCGA-A8-A07B	GNPTAB	DEL	Frame_Shift_Del	12	102164928	A	-	5	90
CRC	TCGA-AA-3672	GNPTAB	SNP	Nonsense_Mutation	12	102158339	G	A	46	50
CRC	TCGA-AA-3845	GNPTAB	SNP	Silent	12	102158709	C	T	23	36
CRC	TCGA-AA-3977	GNPTAB	SNP	Missense_Mutation	12	102155433	G	T	33	67
CRC	TCGA-AA-3977	GNPTAB	SNP	Missense_Mutation	12	102161923	G	A	42	85
CRC	TCGA-AA-A00N	GNPTAB	SNP	Missense_Mutation	12	102155046	A	C	1	59
CRC	TCGA-AA-A010	GNPTAB	SNP	Missense_Mutation	12	102158747	C	T	31	48
AML	TCGA-AB-2813	GNPTAB	SNP	Silent	12	102179965	G	A	36	95
CRC	TCGA-AG-3894	GNPTAB	SNP	Missense_Mutation	12	102183810	C	T	19	99
CRC	TCGA-AG-A002	GNPTAB	SNP	Missense_Mutation	12	102159074	G	T	45	74
BRCA	TCGA-AN-A04D	GNPTAB	SNP	Missense_Mutation	12	102159023	G	C	41	86
BRCA	TCGA-AN-A0XW	GNPTAB	SNP	Missense_Mutation	12	102153831	C	T	30	98
UCEC	TCGA-AP-A056	GNPTAB	SNP	Nonsense_Mutation	12	102164827	C	A	32	99
UCEC	TCGA-AP-A056	GNPTAB	SNP	Missense_Mutation	12	102183810	C	T	19	99
UCEC	TCGA-AP-A056	GNPTAB	SNP	Missense_Mutation	12	102224395	A	C	11	62
UCEC	TCGA-AP-A059	GNPTAB	SNP	Missense_Mutation	12	102158799	C	A	24	50
UCEC	TCGA-AP-A059	GNPTAB	SNP	Missense_Mutation	12	102158940	T	C	61	49
UCEC	TCGA-AP-A059	GNPTAB	SNP	Splice_Site	12	102160073	C	A	24	74
UCEC	TCGA-AP-A0LM	GNPTAB	SNP	Missense_Mutation	12	102140955	C	T	31	62
UCEC	TCGA-AP-A0LM	GNPTAB	SNP	Missense_Mutation	12	102151044	C	T	19	100
UCEC	TCGA-AP-A0LM	GNPTAB	SNP	Nonsense_Mutation	12	102164297	G	A	38	54
UCEC	TCGA-AX-A05Z	GNPTAB	SNP	Missense_Mutation	12	102158702	G	T	35	52
UCEC	TCGA-AX-A0J0	GNPTAB	SNP	Missense_Mutation	12	102158935	C	T	31	99
UCEC	TCGA-AX-A0J0	GNPTAB	SNP	Splice_site	12	102224339	C	T	32	77
UCEC	TCGA-AX-A0J1	GNPTAB	SNP	Missense_Mutation	12	102147186	C	T	31	85
UCEC	TCGA-AX-A0J1	GNPTAB	SNP	Silent	12	102155100	C	T	19	28
KIRC	TCGA-B0-5695	GNPTAB	SNP	Missense_Mutation	12	102163955	A	T	4	50
KIRC	TCGA-B2-5641	GNPTAB	DEL	Frame_Shift_Del	12	102158580	T	-	56	55
UCEC	TCGA-B5-A0JY	GNPTAB	SNP	Silent	12	102155013	A	G	16	52
UCEC	TCGA-B5-A0JY	GNPTAB	SNP	Missense_Mutation	12	102174022	A	C	1	52
UCEC	TCGA-B5-A0K4	GNPTAB	SNP	Nonsense_Mutation	12	102164827	C	A	32	99
UCEC	TCGA-B5-A11E	GNPTAB	SNP	Missense_Mutation	12	102147161	C	A	28	60
UCEC	TCGA-B5-A11J	GNPTAB	SNP	Missense_Mutation	12	102183722	G	A	46	82
UCEC	TCGA-B5-A11N	GNPTAB	SNP	Missense_Mutation	12	102147186	C	T	31	85
UCEC	TCGA-B5-A11N	GNPTAB	SNP	Missense_Mutation	12	102161839	C	T	31	99
HNSC	TCGA-BA-4074	GNPTAB	SNP	Missense_Mutation	12	102151077	A	G	8	91
KIRC	TCGA-BP-4164	GNPTAB	SNP	Silent	12	102161789	C	T	19	44
UCEC	TCGA-BS-A0UF	GNPTAB	SNP	Nonsense_Mutation	12	102158198	C	A	32	59
UCEC	TCGA-BS-A0UF	GNPTAB	SNP	Nonsense_Mutation	12	102174052	C	A	32	99
UCEC	TCGA-BS-A0UJ	GNPTAB	SNP	Missense_Mutation	12	102140979	A	T	16	57
UCEC	TCGA-BS-A0UJ	GNPTAB	SNP	Splice_Site	12	102164365	T	C	55	93
UCEC	TCGA-BS-A0UV	GNPTAB	SNP	Missense_Mutation	12	102158081	C	T	19	51
UCEC	TCGA-BS-A0UV	GNPTAB	SNP	Nonsense_Mutation	12	102174052	C	A	32	99
KIRC	TCGA-CJ-4640	GNPTAB	SNP	Missense_Mutation	12	102151009	C	T	29	100
HNSC	TCGA-CN-5364	GNPTAB	SNP	Missense_Mutation	12	102158435	T	C	52	51
HNSC	TCGA-CQ-5331	GNPTAB	SNP	Nonsense_Mutation	12	102153834	G	A	45	98
HNSC	TCGA-CR-6471	GNPTAB	SNP	Missense_Mutation	12	102153816	G	A	41	98
HNSC	TCGA-CV-7235	GNPTAB	SNP	Missense_Mutation	12	102159938	C	G	27	84
HNSC	TCGA-CV-7253	GNPTAB	SNP	Missense_Mutation	12	102155370	G	C	39	75
KIRC	TCGA-CZ-4853	GNPTAB	SNP	Silent	12	102179968	T	C	59	38
UCEC	TCGA-D1-A0ZV	GNPTAB	SNP	Silent	12	102158901	G	A	41	52
UCEC	TCGA-D1-A101	GNPTAB	SNP	Silent	12	102183790	A	G	8	50
UCEC	TCGA-D1-A103	GNPTAB	SNP	Missense_Mutation	12	102141004	G	A	38	61
UCEC	TCGA-D1-A160	GNPTAB	SNP	Missense_Mutation	12	102164260	A	G	4	92
UCEC	TCGA-D1-A167	GNPTAB	SNP	Missense_Mutation	12	102158602	A	G	14	91
UCEC	TCGA-D1-A16X	GNPTAB	SNP	Missense_Mutation	12	102158935	C	T	31	99
UCEC	TCGA-D1-A17Q	GNPTAB	SNP	Missense_Mutation	12	102147186	C	T	31	85
UCEC	TCGA-DI-A1NN	GNPTAB	SNP	Missense_Mutation	12	102147163	C	T	29	98
BLCA	TCGA-DK-A3IK	GNPTAB	SNP	Nonsense_Mutation	12	102158444	G	A	45	54
BRCA	TCGA-EW-A1IX	GNPTAB	SNP	Missense_Mutation	12	102151069	C	T	32	100