ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0043	RBM11	SNP	Nonsense_Mutation	21	15599435	G	T	45	75
BRCA	BR-MEX-095	RBM11	SNP	Silent	21	15599275	C	G	23	42
ESO	ESO-051	RBM11	SNP	Missense_Mutation	21	15599429	G	A	33	57
HNSC	HN_62646	RBM11	SNP	Missense	21	15599508	G	A	37	63
LUAD	LUAD-B00416	RBM11	SNP	Silent	21	15588565	C	A	23	64
MEL	MEL-JWCI-14	RBM11	SNP	Splice_site	21	15593418	G	A	43	80
MEL	MEL-JWCI-WGS-4	RBM11	SNP	Missense_Mutation	21	15599294	C	T	29	60
MEL	MEL-Ma-Mel-119	RBM11	SNP	Missense_Mutation	21	15596808	C	T	30	60
MEL	MEL-UKRV-Mel-6	RBM11	SNP	Missense_Mutation	21	15599501	A	G	9	63
LUAD	TCGA-17-Z033	RBM11	SNP	Missense_Mutation	21	15599378	G	T	34	55
LUSC	TCGA-34-5236	RBM11	SNP	Missense_Mutation	21	15599537	G	C	45	70
LUSC	TCGA-43-6770	RBM11	SNP	Silent	21	15591904	G	C	45	58
LUAD	TCGA-44-6779	RBM11	SNP	Splice_Site	21	15596757	A	C	3	75
LUSC	TCGA-60-2698	RBM11	SNP	Missense_Mutation	21	15599481	A	G	10	75
LUSC	TCGA-66-2759	RBM11	SNP	Missense_Mutation	21	15591942	T	C	64	82
LUSC	TCGA-70-6722	RBM11	SNP	Missense_Mutation	21	15599595	A	G	3	76
AML	TCGA-AB-2806	RBM11	SNP	Missense_Mutation	21	15599511	A	T	3	77
KIRC	TCGA-AK-3436	RBM11	SNP	Missense_Mutation	21	15592035	A	T	7	70
UCEC	TCGA-AP-A051	RBM11	SNP	Missense_Mutation	21	15599204	T	C	59	58
UCEC	TCGA-AP-A051	RBM11	SNP	Missense_Mutation	21	15599549	G	T	33	82
UCEC	TCGA-AP-A056	RBM11	SNP	Missense_Mutation	21	15599384	C	T	20	74
UCEC	TCGA-AP-A059	RBM11	SNP	Missense_Mutation	21	15591978	C	A	32	89
UCEC	TCGA-AX-A05Z	RBM11	SNP	Missense_Mutation	21	15599387	C	A	30	52
KIRC	TCGA-B0-5705	RBM11	SNP	Nonsense_Mutation	21	15599585	C	T	23	55
BLCA	TCGA-BT-A20R	RBM11	SNP	Missense_Mutation	21	15588577	G	A	33	87
HNSC	TCGA-CV-6945	RBM11	SNP	Missense_Mutation	21	15599316	G	C	41	67
HNSC	TCGA-CV-6945	RBM11	SNP	Missense_Mutation	21	15599442	G	C	41	68
HNSC	TCGA-CV-6945	RBM11	SNP	Missense_Mutation	21	15599531	G	A	45	82
HNSC	TCGA-CV-6945	RBM11	SNP	Nonsense_Mutation	21	15599567	G	T	37	70
HNSC	TCGA-CV-6945	RBM11	SNP	Silent	21	15599599	G	A	33	49
UCEC	TCGA-D1-A16F	RBM11	SNP	Missense_Mutation	21	15588530	C	T	26	67
UCEC	TCGA-D1-A16N	RBM11	SNP	Nonsense_Mutation	21	15599471	C	T	17	76
BLCA	TCGA-DK-A1AC	RBM11	SNP	Silent	21	15599290	G	A	45	41
BLCA	TCGA-DK-A1AC	RBM11	SNP	Silent	21	15599416	G	A	45	42