ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
CRC	CRC-0005	TCF7L2	SNP	Splice_site	10	114912201	T	C	57	90
DLBCL	DLBCL-Ls3200	TCF7L2	SNP	Silent	10	114925524	G	A	38	52
LUAD	LUAD-B02515	TCF7L2	SNP	Missense_Mutation	10	114925341	A	G	14	70
LUAD	LUAD-CHTN-3090346	TCF7L2	SNP	Missense_Mutation	10	114912191	G	T	41	98
LUAD	LUAD-S01306	TCF7L2	SNP	Missense_Mutation	10	114925546	G	A	45	67
MEL	MEL-Ma-Mel-114	TCF7L2	SNP	Missense_Mutation	10	114912128	T	C	53	90
MM	MM-0488	TCF7L2	SNP	Missense_Mutation	10	114903763	C	T	23	100
LUAD	TCGA-05-4396	TCF7L2	SNP	Silent	10	114912184	C	A	23	49
LUAD	TCGA-05-4396	TCF7L2	SNP	Missense_Mutation	10	114920402	G	T	39	95
OV	TCGA-13-0760	TCF7L2	SNP	Missense_Mutation	10	114849161	C	G	26	53
LUAD	TCGA-17-Z020	TCF7L2	SNP	Nonsense_Mutation	10	114925376	C	G	29	100
GBM	TCGA-32-4213	TCF7L2	SNP	Missense_Mutation	10	114711317	T	C	55	80
LUAD	TCGA-44-2656	TCF7L2	SNP	Silent	10	114912190	G	T	43	69
LUAD	TCGA-55-1592	TCF7L2	SNP	Missense_Mutation	10	114925681	G	T	42	58
OV	TCGA-61-2002	TCF7L2	SNP	Missense_Mutation	10	114905822	C	A	22	100
LUSC	TCGA-66-2734	TCF7L2	SNP	Missense_Mutation	10	114911628	G	T	33	71
LUSC	TCGA-66-2768	TCF7L2	SNP	Silent	10	114724335	C	T	25	78
CRC	TCGA-A6-2676	TCF7L2	SNP	Missense_Mutation	10	114925320	A	G	1	76
BRCA	TCGA-A8-A09B	TCF7L2	SNP	Missense_Mutation	10	114849277	T	C	60	71
CRC	TCGA-AA-3530	TCF7L2	INS	Frame_Shift_Ins	10	114925317	-	A	9	57
CRC	TCGA-AA-3672	TCF7L2	DEL	Frame_Shift_Del	10	114849161	C	-	26	53
CRC	TCGA-AA-3673	TCF7L2	SNP	Missense_Mutation	10	114925334	G	A	38	83
CRC	TCGA-AA-3695	TCF7L2	SNP	Nonsense_Mutation	10	114901015	G	T	45	100
CRC	TCGA-AA-3710	TCF7L2	SNP	Silent	10	114911613	C	T	27	49
CRC	TCGA-AA-3845	TCF7L2	SNP	Silent	10	114925476	G	A	38	56
CRC	TCGA-AA-3955	TCF7L2	SNP	Nonsense_Mutation	10	114912149	C	T	27	74
CRC	TCGA-AA-3977	TCF7L2	SNP	Missense_Mutation	10	114911553	C	A	29	83
CRC	TCGA-AA-3977	TCF7L2	SNP	Missense_Mutation	10	114912120	C	T	27	98
CRC	TCGA-AA-3977	TCF7L2	SNP	Missense_Mutation	10	114925333	C	T	31	100
CRC	TCGA-AA-3984	TCF7L2	SNP	Missense_Mutation	10	114911560	T	C	57	91
CRC	TCGA-AA-A00K	TCF7L2	SNP	Missense_Mutation	10	114911545	A	G	13	91
CRC	TCGA-AA-A010	TCF7L2	SNP	Missense_Mutation	10	114925318	A	C	1	92
CRC	TCGA-AA-A01I	TCF7L2	SNP	Nonsense_Mutation	10	114903722	T	G	52	54
CRC	TCGA-AA-A01T	TCF7L2	SNP	Nonsense_Mutation	10	114920448	C	A	25	96
CRC	TCGA-AA-A022	TCF7L2	SNP	Missense_Mutation	10	114925715	C	A	18	97
CRC	TCGA-AF-2692	TCF7L2	INS	Frame_Shift_Ins	10	114901049	-	A	61	92
CRC	TCGA-AG-3582	TCF7L2	SNP	Missense_Mutation	10	114912186	C	T	27	98
CRC	TCGA-AG-3726	TCF7L2	DNP	Missense_Mutation	10	114901010	GC	TT	34	100
CRC	TCGA-AG-3882	TCF7L2	SNP	Missense_Mutation	10	114925333	C	T	31	100
CRC	TCGA-AG-3898	TCF7L2	SNP	Splice_site	10	114901075	G	A	35	100
CRC	TCGA-AG-4007	TCF7L2	SNP	Missense_Mutation	10	114920390	C	A	21	95
CRC	TCGA-AG-A002	TCF7L2	SNP	Silent	10	114912121	G	A	37	42
CRC	TCGA-AG-A016	TCF7L2	INS	Frame_Shift_Ins	10	114925317	-	A	9	57
CRC	TCGA-AG-A02N	TCF7L2	INS	Frame_Shift_Ins	10	114925317	-	A	9	57
CRC	TCGA-AG-A032	TCF7L2	SNP	Nonsense_Mutation	10	114912149	C	T	27	74
BRCA	TCGA-AN-A0XL	TCF7L2	SNP	Silent	10	114849224	T	C	55	59
UCEC	TCGA-AP-A0LM	TCF7L2	SNP	Missense_Mutation	10	114710667	A	G	9	86
UCEC	TCGA-AP-A0LM	TCF7L2	SNP	Splice_site	10	114724315	C	T	28	78
UCEC	TCGA-AX-A05S	TCF7L2	SNP	Silent	10	114901026	G	A	38	51
UCEC	TCGA-AX-A05Z	TCF7L2	SNP	Missense_Mutation	10	114925397	C	T	31	86
UCEC	TCGA-AX-A063	TCF7L2	SNP	Missense_Mutation	10	114901060	G	A	40	76
UCEC	TCGA-AX-A0J1	TCF7L2	SNP	Missense_Mutation	10	114919708	C	T	27	97
UCEC	TCGA-B5-A0JY	TCF7L2	SNP	Silent	10	114910865	C	T	31	52
UCEC	TCGA-B5-A0JY	TCF7L2	SNP	Splice_site	10	114910882	C	T	31	96
HNSC	TCGA-BA-4078	TCF7L2	SNP	Silent	10	114910775	C	T	30	61
BRCA	TCGA-BH-A1FC	TCF7L2	SNP	Missense_Mutation	10	114912185	G	A	38	98
UCEC	TCGA-BS-A0U8	TCF7L2	DEL	In_Frame_Del	10	114710595	AGG	-	7	86
UCEC	TCGA-BS-A0UJ	TCF7L2	SNP	Missense_Mutation	10	114911632	C	T	24	83
UCEC	TCGA-BS-A0UV	TCF7L2	SNP	Missense_Mutation	10	114901057	G	A	37	100
UCEC	TCGA-BS-A0UV	TCF7L2	SNP	Missense_Mutation	10	114911553	C	A	29	83
BRCA	TCGA-C8-A1HI	TCF7L2	SNP	Missense_Mutation	10	114910812	C	T	25	96
KIRC	TCGA-CW-5591	TCF7L2	SNP	Missense_Mutation	10	114901063	G	T	33	100
UCEC	TCGA-D1-A103	TCF7L2	SNP	Silent	10	114912130	C	T	19	51
UCEC	TCGA-D1-A15X	TCF7L2	SNP	Missense_Mutation	10	114910866	G	A	39	72
CARC	Carc-BWH2	TCF7L2	SNP	Missense_Mutation	10	114710634	A	C	12	86