ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
HNSC	HN_62237	FAM46C	SNP	Synonymous	1	118165589	A	G	14	10
MEL	MEL-JWCI-WGS-7	FAM46C	DNP	Missense_Mutation	1	118166443	CC	TT	18	100
MM	MM-0216	FAM46C	SNP	Missense_Mutation	1	118166098	C	G	32	97
MM	MM-0363	FAM46C	SNP	Missense_Mutation	1	118165758	G	C	33	96
MM	MM-0390	FAM46C	SNP	Missense	1	118166034	G	T	41	83
MM	MM-0406	FAM46C	DEL	In_frame_Del	1	118166046	ATC	-	4	88
MM	MM-0408	FAM46C	SNP	Missense	1	118166431	T	G	59	90
MM	MM-0412	FAM46C	DEL	Frame_Shift_Del	1	118165627	TAAC	-	49	89
MM	MM-0421-FIX	FAM46C	SNP	Synonymous	1	118165562	G	T	42	52
MM	MM-0472	FAM46C	SNP	Missense_Mutation	1	118165759	A	G	10	88
MM	MM-0506	FAM46C	SNP	Nonsense_Mutation	1	118165497	G	T	33	60
MM	MM-0507	FAM46C	SNP	Missense_Mutation	1	118165924	T	A	60	88
MM	MM-0529	FAM46C	SNP	Missense_Mutation	1	118166211	G	T	35	100
MM	MM-0546	FAM46C	SNP	Silent	1	118166315	C	T	29	100
MM	MM-0554	FAM46C	SNP	Missense_Mutation	1	118166239	T	G	56	92
MM	MM-0576	FAM46C	SNP	Missense_Mutation	1	118166038	C	G	32	96
MM	MM-0576	FAM46C	SNP	Silent	1	118166117	C	T	23	14
MM	MM-0594	FAM46C	SNP	Missense_Mutation	1	118166059	C	A	32	96
MM	MM-0600	FAM46C	SNP	Missense_Mutation	1	118166042	C	G	30	57
MM	MM-0638	FAM46C	SNP	Nonsense_Mutation	1	118166202	G	T	33	96
LUAD	TCGA-05-4396	FAM46C	SNP	Missense_Mutation	1	118165836	C	A	24	74
LUAD	TCGA-05-4396	FAM46C	SNP	Silent	1	118166117	C	A	23	14
LUAD	TCGA-05-4396	FAM46C	SNP	Missense_Mutation	1	118166139	G	T	39	83
LUAD	TCGA-05-4396	FAM46C	SNP	Missense_Mutation	1	118166214	G	T	39	86
LUAD	TCGA-05-4396	FAM46C	SNP	Missense_Mutation	1	118166248	G	T	39	100
LUAD	TCGA-05-4396	FAM46C	SNP	Missense_Mutation	1	118166326	C	A	23	100
GBM	TCGA-06-0214	FAM46C	SNP	Missense_Mutation	1	118166248	G	A	39	100
GBM	TCGA-06-0241	FAM46C	SNP	Missense_Mutation	1	118165644	G	A	40	82
OV	TCGA-13-1510	FAM46C	SNP	Missense_Mutation	1	118165807	A	T	7	66
GBM	TCGA-16-1045	FAM46C	SNP	Missense_Mutation	1	118166577	G	A	40	86
LUAD	TCGA-17-Z045	FAM46C	SNP	Silent	1	118166264	A	T	7	27
LUSC	TCGA-18-3419	FAM46C	SNP	Missense_Mutation	1	118166109	C	A	21	83
LUAD	TCGA-35-3621	FAM46C	SNP	Missense_Mutation	1	118166014	G	C	40	96
BRCA	TCGA-A8-A09G	FAM46C	SNP	Missense_Mutation	1	118166421	C	T	31	78
CRC	TCGA-AA-3949	FAM46C	SNP	Missense_Mutation	1	118166184	G	A	38	73
BRCA	TCGA-AN-A0FJ	FAM46C	SNP	Missense_Mutation	1	118166379	G	A	38	56
UCEC	TCGA-AX-A060	FAM46C	SNP	Missense_Mutation	1	118165591	C	A	24	97
UCEC	TCGA-B5-A0K2	FAM46C	SNP	Missense_Mutation	1	118165644	G	A	40	82
KIRC	TCGA-B8-5550	FAM46C	SNP	Silent	1	118166327	G	T	39	29
HNSC	TCGA-BB-4227	FAM46C	SNP	Silent	1	118165574	C	A	30	52
UCEC	TCGA-BG-A0LX	FAM46C	SNP	Silent	1	118166654	G	T	46	83
BRCA	TCGA-BH-A0DZ	FAM46C	SNP	Silent	1	118166486	C	T	29	85
UCEC	TCGA-BS-A0TE	FAM46C	SNP	Missense_Mutation	1	118165695	G	A	40	75
UCEC	TCGA-BS-A0UF	FAM46C	SNP	Missense_Mutation	1	118166276	A	C	1	50
HNSC	TCGA-CN-6020	FAM46C	SNP	Missense_Mutation	1	118166445	G	T	40	100
HNSC	TCGA-CR-5248	FAM46C	SNP	Missense_Mutation	1	118166279	C	G	29	86
HNSC	TCGA-CR-7364	FAM46C	SNP	Silent	1	118165682	C	T	29	74
UCEC	TCGA-D1-A103	FAM46C	SNP	Silent	1	118166015	T	C	58	28
UCEC	TCGA-D1-A16F	FAM46C	SNP	Missense_Mutation	1	118166310	T	C	60	92