ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0026	ING1	SNP	Silent	13	111366526	C	T	30	55
CLL	CLL_138	ING1	SNP	Silent	13	111367919	G	A	41	71
ESO	ESO-0071	ING1	SNP	Missense_Mutation	13	111372206	G	A	46	100
ESO	ESO-117	ING1	SNP	Missense_Mutation	13	111367915	C	T	31	46
LUAD	LUAD-AEIUF	ING1	SNP	Missense_Mutation	13	111367831	G	T	37	31
LUAD	LUAD-S01468	ING1	SNP	Missense_Mutation	13	111371668	G	T	38	69
MEL	ME009	ING1	SNP	Splice_site	13	111366632	G	A	35	87
LUAD	TCGA-05-4410	ING1	SNP	Missense_Mutation	13	111371668	G	T	38	69
GBM	TCGA-06-5858	ING1	SNP	Missense_Mutation	13	111371669	C	T	27	99
OV	TCGA-24-1424	ING1	SNP	Missense_Mutation	13	111372144	G	T	44	100
LUSC	TCGA-37-4135	ING1	SNP	Missense_Mutation	13	111368196	G	T	39	57
LUAD	TCGA-50-6590	ING1	DNP	Missense_Mutation	13	111367917	GG	TT	43	41
LUAD	TCGA-55-1595	ING1	SNP	Missense_Mutation	13	111368110	G	T	37	55
UCEC	TCGA-A5-A0VP	ING1	SNP	Missense_Mutation	13	111371713	G	A	40	99
CRC	TCGA-A6-2672	ING1	SNP	Missense_Mutation	13	111371923	G	A	38	71
CRC	TCGA-AA-3949	ING1	SNP	Missense_Mutation	13	111372142	T	C	59	92
CRC	TCGA-AA-A010	ING1	SNP	Missense_Mutation	13	111371944	G	A	37	100
CRC	TCGA-AA-A01F	ING1	SNP	Missense_Mutation	13	111372139	G	A	37	100
CRC	TCGA-AA-A03F	ING1	SNP	Nonsense_Mutation	13	111372025	C	T	27	46
CRC	TCGA-AF-3913	ING1	SNP	Nonsense_Mutation	13	111372025	C	T	27	46
UCEC	TCGA-AP-A056	ING1	SNP	Missense_Mutation	13	111371744	G	A	38	100
UCEC	TCGA-AP-A059	ING1	SNP	Silent	13	111371784	G	A	38	25
UCEC	TCGA-AP-A059	ING1	SNP	Nonsense_Mutation	13	111372144	G	A	44	100
UCEC	TCGA-AP-A0LM	ING1	SNP	Nonsense_Mutation	13	111372025	C	T	27	46
BRCA	TCGA-AR-A1AH	ING1	SNP	Missense_Mutation	13	111371953	G	T	38	54
UCEC	TCGA-B5-A0JY	ING1	SNP	Nonsense_Mutation	13	111372064	G	T	37	85
UCEC	TCGA-B5-A0JZ	ING1	SNP	Silent	13	111372117	C	T	27	40
UCEC	TCGA-B5-A11E	ING1	SNP	Missense_Mutation	13	111371953	G	A	38	54
UCEC	TCGA-B5-A11W	ING1	SNP	Nonsense_Mutation	13	111372025	C	T	27	46
UCEC	TCGA-BG-A0M9	ING1	SNP	Nonsense_Mutation	13	111372127	G	T	37	100
UCEC	TCGA-BS-A0TC	ING1	SNP	Missense_Mutation	13	111372064	G	A	37	85
HNSC	TCGA-CN-6989	ING1	SNP	Silent	13	111371619	C	T	27	28
HNSC	TCGA-CQ-5331	ING1	SNP	Missense_Mutation	13	111372242	T	G	55	92
UCEC	TCGA-D1-A168	ING1	SNP	Nonsense_Mutation	13	111372025	C	T	27	46
UCEC	TCGA-D1-A17C	ING1	SNP	Missense_Mutation	13	111372118	G	T	37	100
UCEC	TCGA-D1-A17D	ING1	SNP	Splice_site	13	111365324	G	T	43	51
UCEC	TCGA-D1-A17Q	ING1	SNP	Missense_Mutation	13	111371951	G	A	42	71
BRCA	TCGA-D8-A1JN	ING1	SNP	Silent	13	111371874	C	T	21	35