ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
LUAD	LUAD-F00018	APOL2	SNP	Missense_Mutation	22	36623740	G	A	44	37
MEL	ME009	APOL2	SNP	Nonsense_Mutation	22	36624241	G	A	47	62
LUAD	TCGA-05-4410	APOL2	INS	In_Frame_Ins	22	36623735	-	GGG	27	52
LUSC	TCGA-39-5035	APOL2	SNP	Missense_Mutation	22	36624152	C	A	24	43
CRC	TCGA-AA-A010	APOL2	SNP	Silent	22	36624107	C	G	17	49
CRC	TCGA-AG-A002	APOL2	SNP	Nonsense_Mutation	22	36627418	C	T	30	70
BRCA	TCGA-AN-A0XW	APOL2	SNP	Missense_Mutation	22	36624084	G	C	33	69
UCEC	TCGA-AP-A051	APOL2	SNP	Missense_Mutation	22	36624081	C	T	26	69
UCEC	TCGA-AP-A056	APOL2	SNP	Missense_Mutation	22	36624250	C	T	31	48
UCEC	TCGA-AP-A0LD	APOL2	SNP	Missense_Mutation	22	36624081	C	T	26	69
BRCA	TCGA-B6-A0I6	APOL2	SNP	Missense_Mutation	22	36623937	C	A	23	46
HNSC	TCGA-CR-7388	APOL2	SNP	Splice_Site	22	36629289	T	C	56	51
UCEC	TCGA-D1-A167	APOL2	SNP	Silent	22	36624251	G	A	40	39
BLCA	TCGA-DK-A1A5	APOL2	SNP	Missense_Mutation	22	36624218	C	G	29	59
BLCA	TCGA-DK-A1A5	APOL2	SNP	Silent	22	36624296	C	G	29	70
BLCA	TCGA-DK-A2I4	APOL2	SNP	Nonsense_Mutation	22	36623580	G	C	45	69
BLCA	TCGA-DK-A2I4	APOL2	SNP	Nonsense_Mutation	22	36623761	G	A	45	51
BLCA	TCGA-DK-A2I4	APOL2	DNP	Missense_Mutation	22	36624083	AG	TA	7	57
HNSC	TCGA-H7-7774	APOL2	SNP	Missense_Mutation	22	36623928	G	A	42	46