ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-007	FAM166A	SNP	Missense_Mutation	9	140139929	C	G	32	58
ESO	ESO-0129	FAM166A	SNP	Splice_Site	9	140140010	C	G	24	77
LUAD	LUAD-CHTN-MAD06-00668	FAM166A	SNP	Splice_Site	9	140140307	T	A	55	76
MEL	ME009	FAM166A	DNP	Nonsense_Mutation	9	140139157	CC	TT	22	70
MEL	MEL-Ma-Mel-48	FAM166A	SNP	Missense_Mutation	9	140139654	C	T	24	53
MM	MM-0364	FAM166A	SNP	Splice_site	9	140139096	G	C	47	72
OV	TCGA-04-1331	FAM166A	SNP	Missense_Mutation	9	140139863	G	C	43	67
OV	TCGA-13-1492	FAM166A	SNP	Missense_Mutation	9	140138237	A	T	8	54
LUSC	TCGA-39-5024	FAM166A	SNP	Splice_site	9	140139670	G	C	34	67
LUSC	TCGA-46-3769	FAM166A	SNP	Missense_Mutation	9	140139971	G	A	34	57
LUAD	TCGA-50-5935	FAM166A	SNP	Missense_Mutation	9	140138730	C	T	32	51
LUSC	TCGA-66-2785	FAM166A	SNP	Silent	9	140140245	C	T	23	20
LUAD	TCGA-91-6829	FAM166A	SNP	Missense_Mutation	9	140139769	C	T	24	51
KIRC	TCGA-A3-3320	FAM166A	SNP	Missense_Mutation	9	140139965	G	A	44	51
AML	TCGA-AB-2854	FAM166A	SNP	Missense_Mutation	9	140140204	C	T	25	61
BRCA	TCGA-AO-A124	FAM166A	SNP	Missense_Mutation	9	140142119	C	T	17	54
UCEC	TCGA-AP-A059	FAM166A	SNP	Silent	9	140139867	C	T	19	39
UCEC	TCGA-B5-A11E	FAM166A	SNP	Missense_Mutation	9	140139660	C	T	25	46
UCEC	TCGA-B5-A11E	FAM166A	SNP	Silent	9	140139957	C	T	24	49
BRCA	TCGA-B6-A0WV	FAM166A	DEL	Frame_Shift_Del	9	140139614	CGTCT	-	27	44
KIRC	TCGA-B8-4621	FAM166A	SNP	Missense_Mutation	9	140139762	G	T	44	52
BRCA	TCGA-BH-A0HP	FAM166A	DEL	Frame_Shift_Del	9	140140154	G	-	47	47
KIRC	TCGA-BP-4161	FAM166A	SNP	Missense_Mutation	9	140140165	T	C	54	59
UCEC	TCGA-BS-A0UF	FAM166A	SNP	Missense_Mutation	9	140140006	A	G	7	53
UCEC	TCGA-BS-A0UF	FAM166A	SNP	Translation_Start_Site	9	140142215	G	T	34	47
BLCA	TCGA-BT-A2LB	FAM166A	SNP	Missense_Mutation	9	140139108	A	G	4	67
BLCA	TCGA-CF-A1HS	FAM166A	SNP	Missense_Mutation	9	140139656	C	G	32	69
BLCA	TCGA-CF-A1HS	FAM166A	SNP	Missense_Mutation	9	140139944	C	G	30	51
HNSC	TCGA-CR-6481	FAM166A	SNP	Missense_Mutation	9	140139845	C	T	32	56
UCEC	TCGA-D1-A167	FAM166A	SNP	Silent	9	140139876	C	T	27	47
HNSC	TCGA-D6-6516	FAM166A	SNP	Missense_Mutation	9	140139886	G	A	43	78
BRCA	TCGA-D8-A140	FAM166A	INS	Frame_Shift_Ins	9	140142146	-	G	31	41
BRCA	TCGA-D8-A27M	FAM166A	SNP	Missense_Mutation	9	140138642	G	C	33	71