ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0025	RSBN1L	SNP	Missense_Mutation	7	77378947	G	A	40	54
ESO	ESO-837	RSBN1L	SNP	Missense_Mutation	7	77378927	A	G	4	45
HNSC	HN_62426	RSBN1L	SNP	Synonymous	7	77325904	C	T	32	55
LUAD	LUAD-74TBW	RSBN1L	SNP	Missense_Mutation	7	77326163	G	C	38	72
LUAD	LUAD-NYU408	RSBN1L	SNP	Missense_Mutation	7	77394879	C	G	25	87
MEL	ME011	RSBN1L	SNP	Missense_Mutation	7	77408344	T	G	63	49
MEL	ME014	RSBN1L	SNP	Silent	7	77379123	C	T	30	56
MEL	MEL-JWCI-WGS-11	RSBN1L	SNP	Missense_Mutation	7	77402516	C	T	23	86
LUAD	TCGA-05-4382	RSBN1L	SNP	Silent	7	77402527	C	G	32	51
LUAD	TCGA-05-4396	RSBN1L	SNP	Missense_Mutation	7	77378834	G	T	39	82
GBM	TCGA-06-0219	RSBN1L	SNP	Nonsense_Mutation	7	77408002	G	A	42	99
GBM	TCGA-06-0881	RSBN1L	SNP	Missense_Mutation	7	77378833	C	T	19	58
LUAD	TCGA-17-Z022	RSBN1L	SNP	Missense_Mutation	7	77398052	G	T	48	87
GBM	TCGA-19-1790	RSBN1L	SNP	Missense_Mutation	7	77402516	C	T	23	86
OV	TCGA-24-2288	RSBN1L	SNP	Missense_Mutation	7	77407993	T	A	60	59
OV	TCGA-25-1329	RSBN1L	SNP	Missense_Mutation	7	77325800	C	T	23	56
LUSC	TCGA-39-5028	RSBN1L	SNP	Missense_Mutation	7	77325886	C	T	23	53
LUSC	TCGA-39-5028	RSBN1L	SNP	Nonsense_Mutation	7	77407731	C	T	25	100
LUAD	TCGA-44-2657	RSBN1L	INS	Frame_Shift_Ins	7	77325829	-	C	42	65
LUSC	TCGA-60-2698	RSBN1L	SNP	Missense_Mutation	7	77408043	C	T	32	63
LUSC	TCGA-66-2744	RSBN1L	SNP	Silent	7	77325946	C	A	27	54
LUAD	TCGA-75-6211	RSBN1L	SNP	Silent	7	77378976	T	C	51	61
CRC	TCGA-AG-A002	RSBN1L	SNP	Missense_Mutation	7	77365830	G	T	33	60
CRC	TCGA-AG-A002	RSBN1L	SNP	Missense_Mutation	7	77379339	G	T	33	70
UCEC	TCGA-AP-A051	RSBN1L	SNP	Missense_Mutation	7	77397997	C	T	19	78
UCEC	TCGA-AP-A056	RSBN1L	SNP	Missense_Mutation	7	77365776	A	C	1	36
UCEC	TCGA-AP-A056	RSBN1L	SNP	Missense_Mutation	7	77394819	G	T	33	100
UCEC	TCGA-AP-A056	RSBN1L	SNP	Missense_Mutation	7	77402502	G	A	37	100
UCEC	TCGA-AX-A05Z	RSBN1L	SNP	Missense_Mutation	7	77408468	G	A	37	91
UCEC	TCGA-AX-A060	RSBN1L	DEL	In_Frame_Del	7	77394895	AGG	-	15	56
UCEC	TCGA-AX-A0J0	RSBN1L	SNP	Nonsense_Mutation	7	77325856	G	T	33	63
UCEC	TCGA-AX-A0J0	RSBN1L	SNP	Silent	7	77365791	A	G	3	67
UCEC	TCGA-AX-A0J0	RSBN1L	SNP	Missense_Mutation	7	77394819	G	T	33	100
KIRC	TCGA-B0-5115	RSBN1L	DEL	Frame_Shift_Del	7	77379172	A	-	11	68
UCEC	TCGA-B5-A0K9	RSBN1L	SNP	Missense_Mutation	7	77326312	G	A	42	55
UCEC	TCGA-B5-A11E	RSBN1L	SNP	Missense_Mutation	7	77408007	T	A	52	90
UCEC	TCGA-BG-A0M0	RSBN1L	SNP	Missense_Mutation	7	77325866	G	A	42	57
UCEC	TCGA-BS-A0TC	RSBN1L	SNP	Missense_Mutation	7	77379139	G	A	37	83
UCEC	TCGA-BS-A0U9	RSBN1L	DEL	In_Frame_Del	7	77394883	TGA	-	63	51
UCEC	TCGA-BS-A0UF	RSBN1L	SNP	Nonsense_Mutation	7	77365774	G	T	33	71
UCEC	TCGA-BS-A0UV	RSBN1L	SNP	Nonsense_Mutation	7	77365774	G	T	33	71
UCEC	TCGA-BS-A0UV	RSBN1L	SNP	Missense_Mutation	7	77365822	G	A	33	71
UCEC	TCGA-BS-A0UV	RSBN1L	SNP	Missense_Mutation	7	77379139	G	A	37	83
BLCA	TCGA-BT-A3PK	RSBN1L	SNP	Missense_Mutation	7	77326204	C	T	29	59
UCEC	TCGA-D1-A15X	RSBN1L	SNP	Missense_Mutation	7	77325866	G	A	42	57
BLCA	TCGA-DK-A1AB	RSBN1L	SNP	Missense_Mutation	7	77408178	C	G	32	90