ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-Ls148	CD79B	SNP	Missense_Mutation	17	62006799	A	C	15	68
DLBCL	DLBCL-Ls1583	CD79B	SNP	Missense_Mutation	17	62006799	A	G	15	68
DLBCL	DLBCL-Ls1683	CD79B	SNP	Missense_Mutation	17	62006799	A	C	15	68
DLBCL	DLBCL-Ls2264	CD79B	SNP	Missense_Mutation	17	62006644	A	G	6	67
DLBCL	DLBCL-Ls2367	CD79B	SNP	Missense_Mutation	17	62009596	A	G	6	50
DLBCL	DLBCL-Ls2596	CD79B	SNP	Missense_Mutation	17	62006799	A	G	15	68
DLBCL	DLBCL-Ls3809	CD79B	SNP	Nonsense_Mutation	17	62006655	A	T	8	37
DLBCL	DLBCL-Ls3809	CD79B	SNP	Missense_Mutation	17	62006798	T	G	57	68
ESO	ESO-0025	CD79B	SNP	Missense_Mutation	17	62006823	C	T	26	52
LUAD	LUAD-B01811	CD79B	SNP	Missense_Mutation	17	62006805	G	T	45	71
LUAD	LUAD-CHTN-3090415	CD79B	SNP	Silent	17	62007507	G	T	33	65
LUAD	LUAD-D01603	CD79B	SNP	Silent	17	62007543	G	A	45	60
LUAD	LUAD-NYU739	CD79B	SNP	Nonsense_Mutation	17	62007560	C	A	31	35
MEL	MEL-Ma-Mel-119	CD79B	SNP	Splice_site	17	62006796	C	T	31	71
MEL	MEL-Ma-Mel-119	CD79B	SNP	Splice_site	17	62006835	C	T	30	71
LUAD	TCGA-05-4417	CD79B	SNP	Missense_Mutation	17	62006601	G	T	44	55
LUSC	TCGA-51-4081	CD79B	SNP	Silent	17	62007148	G	T	33	58
GBM	TCGA-76-6191	CD79B	SNP	Silent	17	62007651	G	A	39	42
BRCA	TCGA-A2-A0YM	CD79B	SNP	Missense_Mutation	17	62007688	A	G	9	43
CRC	TCGA-AG-3726	CD79B	SNP	Missense_Mutation	17	62007479	T	C	59	36
UCEC	TCGA-AP-A056	CD79B	SNP	Missense_Mutation	17	62007698	T	G	62	73
KIRC	TCGA-BP-4983	CD79B	SNP	Silent	17	62009607	C	T	19	51
UCEC	TCGA-BS-A0UV	CD79B	SNP	Missense_Mutation	17	62007560	C	T	31	35
BLCA	TCGA-BT-A3PK	CD79B	SNP	Missense_Mutation	17	62007656	C	T	27	7
BRCA	TCGA-EW-A1J6	CD79B	SNP	Silent	17	62007651	G	A	39	42