ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-MEX-191	FGFR3	SNP	Silent	4	1807598	C	T	29	51
DLBCL	DLBCL-LS4616	FGFR3	SNP	Missense_Mutation	4	1808304	T	G	56	89
HNSC	HN_62686	FGFR3	SNP	Missense	4	1806139	C	G	29	72
LUAD	LUAD-F00365	FGFR3	SNP	Missense_Mutation	4	1806177	G	A	38	56
LUAD	LUAD-S01302	FGFR3	SNP	Missense_Mutation	4	1803661	A	G	10	87
MED	MD-146	FGFR3	SNP	Silent	4	1807640	G	A	43	55
MEL	MEL-JWCI-WGS-7	FGFR3	SNP	Missense_Mutation	4	1808382	G	A	41	97
MEL	MEL-Ma-Mel-35	FGFR3	SNP	Missense_Mutation	4	1803461	G	A	41	95
MM	MM-0433	FGFR3	SNP	Splice_site	4	1808988	G	C	45	60
MM	MM-0478	FGFR3	SNP	Splice_site	4	1808988	G	C	45	60
MM	MM-0484	FGFR3	SNP	Missense_Mutation	4	1807890	A	C	3	76
MM	MM-0526	FGFR3	SNP	Splice_site	4	1803564	C	T	27	65
MM	MM-0557	FGFR3	SNP	Missense_Mutation	4	1801170	C	T	30	82
NB	NB-0433	FGFR3	DEL	Frame_Shift_Del	4	1803593	G	-	39	25
NB	NB-0974	FGFR3	DEL	Frame_Shift_Del	4	1804701	C	-	27	57
LUAD	TCGA-05-4396	FGFR3	SNP	Missense_Mutation	4	1806227	C	A	23	67
LUAD	TCGA-05-4417	FGFR3	SNP	Missense_Mutation	4	1803633	G	A	40	95
GBM	TCGA-06-0168	FGFR3	SNP	Missense_Mutation	4	1807889	A	G	9	89
GBM	TCGA-06-0644	FGFR3	INS	Frame_Shift_Ins	4	1808950	-	C	46	59
GBM	TCGA-19-1790	FGFR3	SNP	Missense_Mutation	4	1807639	G	A	39	96
LUSC	TCGA-21-1078	FGFR3	SNP	Missense_Mutation	4	1803564	C	T	27	65
OV	TCGA-31-1959	FGFR3	SNP	Missense_Mutation	4	1807576	G	T	46	83
GBM	TCGA-32-2498	FGFR3	DEL	Frame_Shift_Del	4	1806181	C	-	26	50
LUSC	TCGA-34-2600	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
LUSC	TCGA-51-4079	FGFR3	SNP	Missense_Mutation	4	1808386	A	T	3	69
LUSC	TCGA-66-2770	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
BRCA	TCGA-A8-A07G	FGFR3	SNP	Missense_Mutation	4	1808375	C	T	18	57
CRC	TCGA-AA-3939	FGFR3	SNP	Missense_Mutation	4	1806176	C	T	27	61
CRC	TCGA-AA-A01R	FGFR3	SNP	Splice_site	4	1808053	G	A	40	97
KIRC	TCGA-AK-3445	FGFR3	SNP	Missense_Mutation	4	1808389	C	A	22	97
UCEC	TCGA-AP-A059	FGFR3	SNP	Missense_Mutation	4	1804671	G	A	40	80
UCEC	TCGA-AP-A059	FGFR3	SNP	Silent	4	1807311	G	A	39	34
UCEC	TCGA-AP-A059	FGFR3	SNP	Missense_Mutation	4	1808652	G	A	40	31
KIRC	TCGA-B0-5109	FGFR3	SNP	Nonsense_Mutation	4	1804696	C	A	31	80
KIRC	TCGA-B2-4101	FGFR3	SNP	Missense_Mutation	4	1808389	C	A	22	97
UCEC	TCGA-B5-A11E	FGFR3	SNP	Missense_Mutation	4	1806243	G	A	37	94
HNSC	TCGA-BB-7872	FGFR3	SNP	Missense_Mutation	4	1807820	G	A	37	96
UCEC	TCGA-BG-A0YV	FGFR3	SNP	Missense_Mutation	4	1808929	C	T	23	31
UCEC	TCGA-BS-A0TA	FGFR3	SNP	Silent	4	1806634	G	A	38	56
UCEC	TCGA-BS-A0UF	FGFR3	SNP	Missense_Mutation	4	1806650	G	A	37	95
UCEC	TCGA-BS-A0UV	FGFR3	SNP	Missense_Mutation	4	1806134	C	A	24	65
BLCA	TCGA-BT-A0S7	FGFR3	SNP	Missense_Mutation	4	1803564	C	T	27	65
BLCA	TCGA-BT-A20T	FGFR3	SNP	Missense_Mutation	4	1806119	G	A	39	81
BLCA	TCGA-BT-A3PK	FGFR3	SNP	Silent	4	1807559	C	T	20	58
BLCA	TCGA-CF-A27C	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
KIRC	TCGA-CJ-4908	FGFR3	SNP	Missense_Mutation	4	1807850	G	T	39	97
HNSC	TCGA-CR-6481	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
HNSC	TCGA-CV-5442	FGFR3	SNP	Missense_Mutation	4	1808852	G	C	41	97
HNSC	TCGA-CV-5442	FGFR3	SNP	Missense_Mutation	4	1808924	G	A	37	98
HNSC	TCGA-CV-6941	FGFR3	SNP	Missense_Mutation	4	1801019	G	A	44	56
HNSC	TCGA-CX-7085	FGFR3	SNP	Missense_Mutation	4	1801486	C	T	31	70
KIRC	TCGA-CZ-4858	FGFR3	SNP	Silent	4	1806217	C	T	17	60
UCEC	TCGA-D1-A167	FGFR3	SNP	Silent	4	1807389	G	A	38	48
UCEC	TCGA-D1-A167	FGFR3	SNP	Missense_Mutation	4	1808391	G	A	38	83
BLCA	TCGA-DK-A1AG	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
BLCA	TCGA-DK-A3IS	FGFR3	SNP	Missense_Mutation	4	1803377	G	A	41	80
BLCA	TCGA-DK-A3IS	FGFR3	SNP	Missense_Mutation	4	1803395	G	A	41	94
BLCA	TCGA-DK-A3IS	FGFR3	SNP	Missense_Mutation	4	1803435	G	A	42	82
BLCA	TCGA-DK-A3IS	FGFR3	DEL	Frame_Shift_Del	4	1808937	C	-	26	98
BLCA	TCGA-E5-A2PC	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95
BLCA	TCGA-G2-A2EO	FGFR3	SNP	Missense_Mutation	4	1806119	G	A	39	81
BLCA	TCGA-H4-A2HQ	FGFR3	SNP	Missense_Mutation	4	1803568	C	G	30	95