ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-LS4616	WT1	SNP	Missense_Mutation	11	32439142	A	C	3	53
ESO	ESO-185	WT1	SNP	Missense_Mutation	11	32456375	C	T	23	73
LUAD	LUAD-S01315	WT1	SNP	Missense_Mutation	11	32450124	G	A	45	98
LUAD	LUAD-TLLGS	WT1	SNP	Splice_site	11	32421496	G	A	45	99
MEL	MEL-JWCI-WGS-1	WT1	DNP	Missense_Mutation	11	32417914	GT	CG	40	59
MEL	MEL-JWCI-WGS-6	WT1	SNP	Missense_Mutation	11	32439146	C	T	29	88
MEL	MEL-Ma-Mel-67	WT1	SNP	Nonsense_Mutation	11	32413596	G	A	47	88
MEL	MEL-Ma-Mel-67	WT1	SNP	Missense_Mutation	11	32417853	T	C	56	94
MEL	MEL-Ma-Mel-94	WT1	SNP	Missense_Mutation	11	32438075	C	T	22	76
MM	MM-0501	WT1	DNP	Splice_Site	11	32439122	CC	TA	18	88
NB	NB-1942	WT1	SNP	Missense_Mutation	11	32410674	C	G	23	100
LUAD	TCGA-05-4382	WT1	SNP	Missense_Mutation	11	32413568	G	A	41	89
LUAD	TCGA-05-4396	WT1	SNP	Silent	11	32413566	G	T	39	70
LUAD	TCGA-05-5425	WT1	SNP	Missense_Mutation	11	32456435	C	T	31	88
GBM	TCGA-12-0615	WT1	SNP	Missense_Mutation	11	32450114	G	A	37	98
LUAD	TCGA-17-Z030	WT1	SNP	Splice_Site	11	32413611	C	A	24	100
LUAD	TCGA-17-Z055	WT1	SNP	Silent	11	32414252	A	G	11	60
GBM	TCGA-27-2528	WT1	SNP	Nonsense_Mutation	11	32413578	G	A	38	67
LUSC	TCGA-34-2596	WT1	SNP	Missense_Mutation	11	32456334	G	C	42	61
LUSC	TCGA-34-5232	WT1	SNP	Silent	11	32450095	G	A	41	50
LUSC	TCGA-43-6647	WT1	SNP	Silent	11	32439176	G	T	43	52
LUSC	TCGA-46-3769	WT1	SNP	Silent	11	32417924	C	A	31	27
LUSC	TCGA-46-3769	WT1	SNP	Missense_Mutation	11	32450097	A	G	2	63
LUAD	TCGA-49-4487	WT1	SNP	Missense_Mutation	11	32450106	C	A	25	64
LUAD	TCGA-49-4505	WT1	SNP	Missense_Mutation	11	32414287	G	T	47	100
LUAD	TCGA-50-5941	WT1	SNP	Missense_Mutation	11	32413601	G	T	47	100
LUAD	TCGA-55-1592	WT1	SNP	Splice_site	11	32413610	C	A	18	100
LUSC	TCGA-60-2719	WT1	SNP	Missense_Mutation	11	32421532	A	C	16	91
LUAD	TCGA-64-5775	WT1	SNP	Missense_Mutation	11	32414272	C	A	30	100
LUAD	TCGA-64-5781	WT1	SNP	Missense_Mutation	11	32413565	C	A	23	100
LUSC	TCGA-66-2727	WT1	SNP	Missense_Mutation	11	32439126	T	G	56	82
GBM	TCGA-76-6660	WT1	SNP	Silent	11	32421505	T	G	55	64
LUAD	TCGA-86-6562	WT1	SNP	Silent	11	32456382	G	C	46	68
KIRC	TCGA-A3-3326	WT1	SNP	Missense_Mutation	11	32421532	A	T	16	91
CRC	TCGA-A6-2672	WT1	SNP	Missense_Mutation	11	32413565	C	T	23	100
CRC	TCGA-AA-3544	WT1	SNP	Missense_Mutation	11	32421519	G	A	40	99
CRC	TCGA-AA-3710	WT1	SNP	Silent	11	32410610	C	T	27	48
CRC	TCGA-AA-3715	WT1	SNP	Missense_Mutation	11	32413574	T	G	56	72
CRC	TCGA-AA-3930	WT1	SNP	Missense_Mutation	11	32410683	T	C	56	93
CRC	TCGA-AA-3941	WT1	SNP	Silent	11	32421569	G	A	38	40
AML	TCGA-AB-2839	WT1	INS	Frame_Shift_Ins	11	32417908	-	CCGA	26	63
AML	TCGA-AB-2844	WT1	INS	Frame_Shift_Ins	11	32417910	-	ACCGTACA	37	96
AML	TCGA-AB-2846	WT1	INS	Frame_Shift_Ins	11	32417909	-	A	23	24
AML	TCGA-AB-2874	WT1	SNP	Missense_Mutation	11	32413566	G	A	39	70
AML	TCGA-AB-2905	WT1	INS	Frame_Shift_Ins	11	32417922	-	TCGGGGCTAC	36	88
AML	TCGA-AB-2913	WT1	SNP	Splice_Site	11	32417802	C	G	18	100
AML	TCGA-AB-2919	WT1	SNP	Missense_Mutation	11	32413557	G	A	47	100
AML	TCGA-AB-2930	WT1	INS	Frame_Shift_Ins	11	32417941	-	A	17	100
AML	TCGA-AB-2970	WT1	SNP	Splice_Site	11	32413611	C	T	24	100
AML	TCGA-AB-2976	WT1	INS	Frame_Shift_Ins	11	32417909	-	GACCG	23	24
AML	TCGA-AB-2989	WT1	DEL	Frame_Shift_Del	11	32417846	AT	-	4	51
AML	TCGA-AB-3009	WT1	INS	Frame_Shift_Ins	11	32417909	-	GACCG	23	24
CRC	TCGA-AF-2692	WT1	SNP	Silent	11	32421575	G	A	40	44
CRC	TCGA-AG-A002	WT1	SNP	Missense_Mutation	11	32421570	C	T	28	63
CRC	TCGA-AG-A02N	WT1	SNP	Missense_Mutation	11	32450156	G	A	40	84
UCEC	TCGA-AP-A051	WT1	SNP	Silent	11	32450098	C	T	20	76
BRCA	TCGA-AR-A1AJ	WT1	SNP	Silent	11	32450119	C	T	27	51
UCEC	TCGA-B5-A11E	WT1	SNP	Silent	11	32421518	C	T	27	42
UCEC	TCGA-BG-A0VW	WT1	SNP	Missense_Mutation	11	32410656	C	T	27	100
BRCA	TCGA-BH-A18P	WT1	SNP	Missense_Mutation	11	32414250	C	T	19	100
KIRC	TCGA-BP-4803	WT1	DEL	Frame_Shift_Del	11	32456513	CC	-	26	54
KIRC	TCGA-BP-5175	WT1	SNP	Missense_Mutation	11	32417899	T	A	58	62
UCEC	TCGA-BS-A0UV	WT1	SNP	Missense_Mutation	11	32417914	G	A	40	59
BLCA	TCGA-BT-A2LB	WT1	SNP	Splice_site	11	32410605	C	G	29	62
BRCA	TCGA-C8-A27B	WT1	SNP	Missense_Mutation	11	32410657	G	A	39	100
HNSC	TCGA-CV-7427	WT1	SNP	Silent	11	32417879	G	A	45	70
UCEC	TCGA-D1-A167	WT1	SNP	Missense_Mutation	11	32413565	C	A	23	100