ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-MAYO_DLBCL_234	RBM26	SNP	Missense_Mutation	13	79916873	T	C	57	76
ESO	ESO-0079	RBM26	SNP	Missense_Mutation	13	79951570	C	T	24	81
ESO	ESO-0176	RBM26	SNP	Nonsense_Mutation	13	79945089	G	A	40	70
HNSC	HN_62854	RBM26	SNP	Splice_site	13	79928576	G	C	45	90
LUAD	LUAD-E01278	RBM26	SNP	Missense_Mutation	13	79939719	G	T	44	96
LUAD	LUAD-NYU669	RBM26	SNP	Missense_Mutation	13	79908548	T	A	56	75
LUAD	LUAD-NYU776	RBM26	SNP	Silent	13	79932421	C	T	21	58
LUAD	LUAD-NYU776	RBM26	SNP	Missense_Mutation	13	79940801	C	A	24	83
MEL	ME009	RBM26	SNP	Missense_Mutation	13	79918911	C	T	21	94
MEL	MEL-Ma-Mel-35	RBM26	SNP	Silent	13	79933760	G	A	47	43
MM	MM-0579	RBM26	SNP	Missense_Mutation	13	79911400	C	G	32	95
LUAD	TCGA-05-4410	RBM26	SNP	Silent	13	79929484	G	A	41	54
OV	TCGA-13-1499	RBM26	SNP	Silent	13	79933778	T	G	55	62
LUAD	TCGA-17-Z014	RBM26	SNP	Missense_Mutation	13	79942937	G	A	45	100
LUSC	TCGA-21-1070	RBM26	SNP	Silent	13	79940805	C	T	27	50
LUSC	TCGA-39-5022	RBM26	SNP	Silent	13	79979847	G	C	37	58
LUSC	TCGA-66-2792	RBM26	SNP	Nonsense_Mutation	13	79946001	G	C	45	94
BRCA	TCGA-A1-A0SE	RBM26	INS	Frame_Shift_Ins	13	79945989	-	A	57	86
UCEC	TCGA-A5-A0VP	RBM26	SNP	Missense_Mutation	13	79943050	G	A	37	82
BRCA	TCGA-A8-A09N	RBM26	SNP	Missense_Mutation	13	79932554	C	G	32	72
CRC	TCGA-AA-3977	RBM26	SNP	Nonsense_Mutation	13	79929465	C	A	32	99
CRC	TCGA-AA-A004	RBM26	SNP	Missense_Mutation	13	79894769	G	C	33	94
CRC	TCGA-AA-A010	RBM26	SNP	Splice_site	13	79894757	C	A	29	94
CRC	TCGA-AG-3883	RBM26	SNP	Missense_Mutation	13	79932499	C	A	28	62
CRC	TCGA-AG-4005	RBM26	SNP	Nonsense_Mutation	13	79911344	G	A	38	65
CRC	TCGA-AG-A002	RBM26	SNP	Missense_Mutation	13	79932564	T	G	64	89
BRCA	TCGA-AN-A0FL	RBM26	SNP	Missense_Mutation	13	79928636	G	C	41	98
UCEC	TCGA-AP-A051	RBM26	SNP	Missense_Mutation	13	79952962	G	A	46	100
UCEC	TCGA-AP-A0LM	RBM26	SNP	Missense_Mutation	13	79945124	C	A	32	94
UCEC	TCGA-AP-A0LM	RBM26	SNP	Missense_Mutation	13	79945144	C	A	32	55
UCEC	TCGA-AP-A0LT	RBM26	SNP	Missense_Mutation	13	79940321	G	T	35	99
UCEC	TCGA-AX-A05Y	RBM26	SNP	Missense_Mutation	13	79945232	C	T	31	95
UCEC	TCGA-AX-A05Z	RBM26	SNP	Nonsense_Mutation	13	79951537	C	A	32	83
UCEC	TCGA-AX-A0J0	RBM26	SNP	Missense_Mutation	13	79911337	C	T	31	95
UCEC	TCGA-B5-A11E	RBM26	SNP	Missense_Mutation	13	79911257	C	A	32	83
UCEC	TCGA-B5-A11E	RBM26	SNP	Missense_Mutation	13	79933756	C	T	21	96
UCEC	TCGA-B5-A11E	RBM26	SNP	Missense_Mutation	13	79939715	C	A	32	96
UCEC	TCGA-B5-A11E	RBM26	SNP	Missense_Mutation	13	79945256	C	A	32	95
UCEC	TCGA-B5-A11N	RBM26	SNP	Missense_Mutation	13	79951531	C	A	32	100
BRCA	TCGA-B6-A0I9	RBM26	SNP	Silent	13	79911273	C	T	23	46
HNSC	TCGA-BA-4075	RBM26	SNP	Missense_Mutation	13	79911341	C	A	24	95
HNSC	TCGA-BA-5152	RBM26	SNP	Missense_Mutation	13	79911392	G	A	45	81
HNSC	TCGA-BA-5558	RBM26	SNP	Missense_Mutation	13	79933752	G	A	33	76
UCEC	TCGA-BG-A0LX	RBM26	SNP	Missense_Mutation	13	79952962	G	A	46	100
BRCA	TCGA-BH-A203	RBM26	SNP	Silent	13	79896574	G	A	45	63
BLCA	TCGA-BL-A3JM	RBM26	SNP	Missense_Mutation	13	79942951	C	A	20	85
KIRC	TCGA-BP-5010	RBM26	SNP	Missense_Mutation	13	79911406	C	G	23	95
UCEC	TCGA-BS-A0UF	RBM26	SNP	Missense_Mutation	13	79896579	G	A	37	89
UCEC	TCGA-BS-A0UF	RBM26	SNP	Missense_Mutation	13	79929432	C	A	20	99
UCEC	TCGA-BS-A0UF	RBM26	SNP	Missense_Mutation	13	79939776	C	T	20	96
UCEC	TCGA-BS-A0UJ	RBM26	SNP	Silent	13	79940775	A	G	7	63
BLCA	TCGA-BT-A20R	RBM26	SNP	Missense_Mutation	13	79939829	T	C	52	88
BLCA	TCGA-BT-A2LA	RBM26	SNP	Missense_Mutation	13	79894806	C	G	32	94
BLCA	TCGA-BT-A3PJ	RBM26	SNP	Missense_Mutation	13	79943007	C	G	29	57
BLCA	TCGA-CF-A27C	RBM26	SNP	Nonsense_Mutation	13	79916956	G	C	45	84
KIRC	TCGA-CJ-4912	RBM26	SNP	Missense_Mutation	13	79940847	A	C	9	70
HNSC	TCGA-CN-4742	RBM26	DEL	Frame_Shift_Del	13	79943084	CTGTTCTA	-	32	96
HNSC	TCGA-CN-6011	RBM26	SNP	Splice_Site	13	79911235	A	G	14	88
HNSC	TCGA-CN-6013	RBM26	SNP	Missense_Mutation	13	79894788	C	T	32	94
HNSC	TCGA-CN-6024	RBM26	SNP	Silent	13	79945213	G	A	44	49
HNSC	TCGA-CQ-5326	RBM26	SNP	Missense_Mutation	13	79940220	G	A	41	84
HNSC	TCGA-CR-6481	RBM26	SNP	Missense_Mutation	13	79952987	C	G	32	100
HNSC	TCGA-CV-6954	RBM26	SNP	Missense_Mutation	13	79896555	G	C	36	62
UCEC	TCGA-D1-A16E	RBM26	SNP	Nonsense_Mutation	13	79911350	G	A	38	59
BLCA	TCGA-DK-A2HX	RBM26	SNP	Missense_Mutation	13	79945293	G	A	39	65
BLCA	TCGA-DK-A2I4	RBM26	SNP	Missense_Mutation	13	79942973	G	T	45	98
BLCA	TCGA-DK-A2I4	RBM26	SNP	Missense_Mutation	13	79943032	G	C	33	98
UCEC	TCGA-E6-A1LZ	RBM26	SNP	Missense_Mutation	13	79940204	G	C	33	94
BLCA	TCGA-FD-A3B5	RBM26	SNP	Missense_Mutation	13	79945269	G	A	37	95