ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-Ls2367	INTS12	SNP	Missense_Mutation	4	106604396	C	G	28	98
LUAD	LUAD-S01478	INTS12	SNP	Missense_Mutation	4	106614616	C	G	29	99
MM	MM-0389	INTS12	SNP	Missense	4	106603944	C	T	29	100
MM	MM-0578	INTS12	SNP	Splice_site	4	106621162	T	C	52	90
MM	MM-0633	INTS12	SNP	Splice_site	4	106621162	T	C	52	90
LUAD	TCGA-05-4396	INTS12	SNP	Missense_Mutation	4	106614593	C	A	21	55
GBM	TCGA-28-2502	INTS12	SNP	Missense_Mutation	4	106604288	C	T	17	74
LUAD	TCGA-38-4629	INTS12	SNP	Splice_site	4	106621161	A	G	8	90
LUAD	TCGA-64-1677	INTS12	SNP	Splice_site	4	106616825	C	G	30	90
LUAD	TCGA-80-5611	INTS12	SNP	Missense_Mutation	4	106603997	G	A	41	49
BRCA	TCGA-A8-A07L	INTS12	SNP	Missense_Mutation	4	106613283	C	T	21	22
CRC	TCGA-AA-3672	INTS12	SNP	Splice_site	4	106607849	C	A	24	100
CRC	TCGA-AA-A00R	INTS12	SNP	Missense_Mutation	4	106604196	T	G	60	53
UCEC	TCGA-AP-A059	INTS12	SNP	Missense_Mutation	4	106607985	G	T	36	88
UCEC	TCGA-AX-A05Z	INTS12	SNP	Missense_Mutation	4	106607862	C	A	32	100
UCEC	TCGA-AX-A0J0	INTS12	SNP	Nonsense_Mutation	4	106614540	A	C	13	91
HNSC	TCGA-BA-6872	INTS12	DEL	Frame_Shift_Del	4	106604428	G	-	37	98
UCEC	TCGA-BS-A0UF	INTS12	SNP	Silent	4	106613190	C	T	31	56
BLCA	TCGA-BT-A20J	INTS12	SNP	Missense_Mutation	4	106614616	C	G	29	99
HNSC	TCGA-CN-5363	INTS12	SNP	Missense_Mutation	4	106604207	C	T	17	62
HNSC	TCGA-CN-6010	INTS12	SNP	Missense_Mutation	4	106621142	C	A	21	75
HNSC	TCGA-CQ-6224	INTS12	SNP	Missense_Mutation	4	106621141	C	T	30	99
UCEC	TCGA-D1-A160	INTS12	SNP	Missense_Mutation	4	106616710	T	C	56	84
UCEC	TCGA-D1-A17U	INTS12	SNP	Missense_Mutation	4	106604429	A	T	11	75
BRCA	TCGA-D8-A1JS	INTS12	SNP	Silent	4	106604454	T	A	62	54
BLCA	TCGA-DK-A3IS	INTS12	SNP	Silent	4	106603932	C	T	32	56
HNSC	TCGA-DQ-7595	INTS12	SNP	Missense_Mutation	4	106604042	T	G	53	55
BRCA	TCGA-E9-A22E	INTS12	SNP	Missense_Mutation	4	106614625	C	T	29	81
BLCA	TCGA-GD-A3OP	INTS12	SNP	Missense_Mutation	4	106614625	C	T	29	81