ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0071	APAF1	SNP	Missense_Mutation	12	99117517	C	T	32	86
CRC	CRC-0009	APAF1	SNP	Missense	12	99065416	C	T	23	85
CLL	CW141	APAF1	SNP	Missense_Mutation	12	99071249	C	G	21	99
DLBCL	DLBCL-Ls3245	APAF1	SNP	Silent	12	99117446	A	G	1	51
HNSC	HN_00190	APAF1	SNP	Missense	12	99064850	A	G	16	60
LUAD	LUAD-5V8LT	APAF1	SNP	Missense_Mutation	12	99059437	G	T	41	69
MEL	ME002	APAF1	SNP	Splice_site	12	99126198	T	C	59	74
MM	MM-0514	APAF1	SNP	Missense_Mutation	12	99121087	A	G	16	57
RHAB	Rhabdoid-09-044	APAF1	SNP	Missense_Mutation	12	99061359	G	T	35	53
LUAD	TCGA-05-4396	APAF1	SNP	Silent	12	99119294	G	T	39	45
LUAD	TCGA-05-4396	APAF1	SNP	Missense_Mutation	12	99120994	C	A	23	64
LUAD	TCGA-05-4432	APAF1	SNP	Missense_Mutation	12	99074148	A	G	16	57
OV	TCGA-09-1665	APAF1	SNP	Missense_Mutation	12	99061363	G	A	33	95
OV	TCGA-13-0923	APAF1	SNP	Missense_Mutation	12	99043373	A	T	9	62
LUAD	TCGA-17-Z004	APAF1	SNP	Splice_Site	12	99109204	G	T	33	90
LUAD	TCGA-17-Z022	APAF1	SNP	Silent	12	99106159	C	T	28	52
LUAD	TCGA-17-Z046	APAF1	SNP	Splice_Site	12	99056233	G	T	35	98
LUSC	TCGA-22-4613	APAF1	SNP	Missense_Mutation	12	99042501	G	T	41	81
LUAD	TCGA-38-4625	APAF1	SNP	Missense_Mutation	12	99097167	A	T	15	55
LUSC	TCGA-39-5022	APAF1	SNP	Missense_Mutation	12	99077009	A	G	8	57
LUAD	TCGA-50-5044	APAF1	SNP	Silent	12	99056294	G	A	36	51
LUAD	TCGA-50-5045	APAF1	DEL	Frame_Shift_Del	12	99061359	G	-	35	53
LUSC	TCGA-66-2766	APAF1	SNP	Missense_Mutation	12	99056574	A	T	3	57
LUSC	TCGA-66-2788	APAF1	SNP	Missense_Mutation	12	99061383	C	G	20	51
LUAD	TCGA-67-4679	APAF1	SNP	Silent	12	99053024	C	A	19	82
LUSC	TCGA-85-6561	APAF1	SNP	Silent	12	99076989	C	T	26	61
LUAD	TCGA-91-6828	APAF1	SNP	Missense_Mutation	12	99097244	G	T	47	62
CRC	TCGA-A6-2676	APAF1	SNP	Silent	12	99071221	G	A	37	76
CRC	TCGA-AA-3548	APAF1	SNP	Silent	12	99061305	G	A	33	53
CRC	TCGA-AA-3715	APAF1	SNP	Missense_Mutation	12	99065359	G	A	41	99
CRC	TCGA-AA-3833	APAF1	SNP	Missense_Mutation	12	99097192	C	T	19	55
CRC	TCGA-AA-3877	APAF1	INS	Frame_Shift_Ins	12	99071207	-	A	5	78
CRC	TCGA-AA-3977	APAF1	SNP	Missense_Mutation	12	99093220	G	T	34	65
CRC	TCGA-AA-3977	APAF1	SNP	Splice_site	12	99097277	G	A	35	89
CRC	TCGA-AA-3984	APAF1	SNP	Silent	12	99071221	G	A	37	76
CRC	TCGA-AA-A00N	APAF1	SNP	Missense_Mutation	12	99064795	A	C	1	55
CRC	TCGA-AA-A010	APAF1	SNP	Missense_Mutation	12	99056319	G	T	33	82
CRC	TCGA-AA-A010	APAF1	SNP	Missense_Mutation	12	99060074	G	A	40	43
UCEC	TCGA-AP-A051	APAF1	SNP	Nonsense_Mutation	12	99074073	G	T	35	97
UCEC	TCGA-AP-A054	APAF1	SNP	Splice_Site	12	99080653	T	C	57	87
UCEC	TCGA-AP-A056	APAF1	SNP	Missense_Mutation	12	99064761	C	A	28	65
UCEC	TCGA-AX-A05Z	APAF1	SNP	Missense_Mutation	12	99059507	G	T	33	70
UCEC	TCGA-B5-A0JR	APAF1	SNP	Missense_Mutation	12	99117070	T	C	58	66
UCEC	TCGA-B5-A0JY	APAF1	SNP	Missense_Mutation	12	99059430	G	T	33	86
UCEC	TCGA-B5-A0JY	APAF1	SNP	Splice_Site	12	99093185	G	T	34	88
UCEC	TCGA-B5-A11E	APAF1	SNP	Missense_Mutation	12	99053025	G	A	39	97
UCEC	TCGA-B5-A11E	APAF1	SNP	Nonsense_Mutation	12	99126246	G	T	47	94
UCEC	TCGA-BG-A0MS	APAF1	SNP	Missense_Mutation	12	99053093	C	T	23	82
BRCA	TCGA-BH-A0HP	APAF1	SNP	Missense_Mutation	12	99042512	C	T	32	65
BRCA	TCGA-BH-A1FC	APAF1	SNP	Missense_Mutation	12	99074109	G	A	45	97
UCEC	TCGA-BS-A0UF	APAF1	SNP	Missense_Mutation	12	99052985	A	G	5	75
UCEC	TCGA-BS-A0UF	APAF1	SNP	Missense_Mutation	12	99074172	A	C	1	76
UCEC	TCGA-BS-A0UF	APAF1	SNP	Nonsense_Mutation	12	99102435	G	T	33	70
UCEC	TCGA-BS-A0UJ	APAF1	SNP	Missense_Mutation	12	99042441	T	C	51	53
UCEC	TCGA-BS-A0UV	APAF1	SNP	Missense_Mutation	12	99043444	G	T	33	84
BLCA	TCGA-BT-A3PK	APAF1	SNP	Silent	12	99076995	C	T	29	49
HNSC	TCGA-CN-4723	APAF1	SNP	Missense_Mutation	12	99077046	C	A	30	52
HNSC	TCGA-CN-4739	APAF1	SNP	Missense_Mutation	12	99056498	A	G	1	89
HNSC	TCGA-CN-6019	APAF1	SNP	Nonsense_Mutation	12	99065373	C	T	19	76
HNSC	TCGA-CN-6024	APAF1	SNP	Missense_Mutation	12	99060113	A	G	11	88
HNSC	TCGA-CN-6995	APAF1	SNP	Missense_Mutation	12	99056319	G	T	33	82
HNSC	TCGA-CR-6484	APAF1	SNP	Missense_Mutation	12	99093306	G	A	45	89
HNSC	TCGA-CV-6954	APAF1	SNP	Missense_Mutation	12	99042256	A	T	11	89
HNSC	TCGA-CV-7178	APAF1	SNP	Missense_Mutation	12	99060002	A	T	9	88
UCEC	TCGA-D1-A103	APAF1	SNP	Missense_Mutation	12	99060022	G	A	41	96
UCEC	TCGA-D1-A160	APAF1	SNP	Silent	12	99042272	T	C	51	54
UCEC	TCGA-D1-A16X	APAF1	SNP	Missense_Mutation	12	99071208	A	C	1	90
UCEC	TCGA-D1-A17Q	APAF1	SNP	Missense_Mutation	12	99052986	A	C	1	76
BRCA	TCGA-E9-A1N3	APAF1	SNP	Missense_Mutation	12	99074131	C	G	32	97
BLCA	TCGA-G2-A2ES	APAF1	SNP	Missense_Mutation	12	99120994	C	T	23	64
HNSC	TCGA-HL-7533	APAF1	SNP	Missense_Mutation	12	99053108	C	T	31	84