ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-0029	ITGB7	SNP	Silent	12	53589828	C	T	20	52
LUAD	LUAD-S01315	ITGB7	SNP	Missense_Mutation	12	53588053	C	T	29	60
MEL	MEL-Ma-Mel-119	ITGB7	SNP	Silent	12	53588060	G	A	43	52
MEL	MEL-Ma-Mel-63	ITGB7	SNP	Missense_Mutation	12	53587995	C	T	31	49
LUAD	TCGA-05-4426	ITGB7	SNP	Missense_Mutation	12	53586306	C	A	21	51
GBM	TCGA-06-0882	ITGB7	SNP	Missense_Mutation	12	53590514	C	T	27	51
GBM	TCGA-12-5295	ITGB7	SNP	Missense_Mutation	12	53585372	G	A	37	51
OV	TCGA-13-0717	ITGB7	SNP	Missense	12	53591327	C	G	22	95
OV	TCGA-13-0923	ITGB7	SNP	Missense_Mutation	12	53591298	C	T	20	62
LUSC	TCGA-22-5472	ITGB7	SNP	Silent	12	53585733	C	A	21	54
OV	TCGA-23-1023	ITGB7	SNP	Missense_Mutation	12	53585702	A	G	15	74
OV	TCGA-25-1318	ITGB7	SNP	Missense	12	53591327	C	G	22	95
GBM	TCGA-32-2638	ITGB7	SNP	Missense_Mutation	12	53590523	C	T	23	64
LUSC	TCGA-33-6737	ITGB7	SNP	Missense_Mutation	12	53589169	C	T	30	74
LUSC	TCGA-60-2698	ITGB7	SNP	Silent	12	53590369	G	T	33	57
OV	TCGA-61-2097	ITGB7	SNP	Silent	12	53589942	G	A	45	61
CRC	TCGA-AA-3542	ITGB7	SNP	Missense_Mutation	12	53591327	C	G	22	95
CRC	TCGA-AA-3864	ITGB7	SNP	Missense_Mutation	12	53586536	C	T	23	82
CRC	TCGA-AA-3864	ITGB7	SNP	Silent	12	53588114	G	A	39	30
CRC	TCGA-AA-3869	ITGB7	SNP	Silent	12	53586154	G	A	40	43
CRC	TCGA-AA-3984	ITGB7	SNP	Missense_Mutation	12	53594136	G	T	42	59
CRC	TCGA-AA-A01Q	ITGB7	SNP	Missense_Mutation	12	53586224	A	G	12	50
AML	TCGA-AB-2863	ITGB7	SNP	Silent	12	53594183	G	A	46	55
UCEC	TCGA-AP-A051	ITGB7	SNP	Missense_Mutation	12	53585680	C	T	27	77
KIRC	TCGA-B0-4691	ITGB7	SNP	Missense_Mutation	12	53586257	G	C	42	58
KIRC	TCGA-B0-4814	ITGB7	SNP	Missense_Mutation	12	53591327	C	G	22	95
UCEC	TCGA-B5-A0JY	ITGB7	SNP	Missense_Mutation	12	53587995	C	T	31	49
UCEC	TCGA-B5-A11E	ITGB7	SNP	Missense_Mutation	12	53594184	C	T	28	81
BRCA	TCGA-BH-A0DK	ITGB7	SNP	Silent	12	53587622	G	T	39	59
HNSC	TCGA-CR-7367	ITGB7	SNP	Missense_Mutation	12	53590515	G	A	38	57
KIRC	TCGA-CZ-5467	ITGB7	SNP	Silent	12	53594099	C	T	18	46
UCEC	TCGA-D1-A103	ITGB7	SNP	Missense_Mutation	12	53585680	C	T	27	77
UCEC	TCGA-D1-A103	ITGB7	SNP	Missense_Mutation	12	53589872	G	A	46	77
HNSC	TCGA-D6-6516	ITGB7	SNP	Silent	12	53589185	C	T	21	59