ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
HNSC	HN_62854	PBLD	SNP	Synonymous	10	70056072	G	T	33	56
LUAD	LUAD-CHTN-3090346	PBLD	SNP	Missense_Mutation	10	70066540	G	A	34	85
LUAD	LUAD-S01306	PBLD	SNP	Nonsense_Mutation	10	70048408	C	A	30	73
MEL	MEL-13561	PBLD	SNP	Silent	10	70051946	C	T	22	64
MEL	MEL-Ma-Mel-67	PBLD	SNP	Missense_Mutation	10	70044002	G	A	37	54
LUAD	TCGA-05-4249	PBLD	DEL	Frame_Shift_Del	10	70048359	CCTGTGTTTTCAACTTG	-	22	84
LUAD	TCGA-05-4396	PBLD	SNP	Silent	10	70048388	C	A	23	48
LUAD	TCGA-05-4396	PBLD	SNP	Missense_Mutation	10	70056663	G	T	39	87
LUAD	TCGA-05-4417	PBLD	SNP	Missense_Mutation	10	70056663	G	T	39	87
LUSC	TCGA-21-1070	PBLD	SNP	Missense_Mutation	10	70048725	G	C	47	58
LUSC	TCGA-39-5019	PBLD	SNP	Silent	10	70051922	G	T	37	38
LUAD	TCGA-50-5933	PBLD	SNP	Missense_Mutation	10	70048269	C	A	21	84
OV	TCGA-61-1995	PBLD	SNP	Missense_Mutation	10	70051944	G	T	42	72
LUSC	TCGA-66-2768	PBLD	SNP	Missense_Mutation	10	70043999	G	T	41	48
LUAD	TCGA-91-6829	PBLD	SNP	Silent	10	70056647	T	A	59	50
CRC	TCGA-AA-3543	PBLD	SNP	Missense_Mutation	10	70048302	G	T	46	52
CRC	TCGA-AA-A00A	PBLD	SNP	Silent	10	70043970	A	G	6	22
UCEC	TCGA-AP-A0LD	PBLD	SNP	Silent	10	70048415	C	T	19	45
UCEC	TCGA-AP-A0LM	PBLD	SNP	Silent	10	70051967	G	A	45	55
UCEC	TCGA-AX-A05Z	PBLD	SNP	Missense_Mutation	10	70045062	G	A	37	46
KIRC	TCGA-CJ-5671	PBLD	SNP	Missense_Mutation	10	70056040	A	C	6	67
HNSC	TCGA-CR-7390	PBLD	SNP	Missense_Mutation	10	70044029	G	C	39	74
UCEC	TCGA-D1-A101	PBLD	SNP	Missense_Mutation	10	70043987	C	T	18	75
UCEC	TCGA-DI-A0WH	PBLD	SNP	Splice_Site	10	70051885	C	G	18	72
BLCA	TCGA-DK-A1AE	PBLD	SNP	Missense_Mutation	10	70048339	G	C	33	58
BLCA	TCGA-DK-A3IS	PBLD	SNP	Nonsense_Mutation	10	70044041	G	A	45	87