ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-H01	KRT35	SNP	Missense_Mutation	17	39637240	C	A	25	55
HNSC	HN_62493	KRT35	SNP	Missense	17	39633366	G	A	42	50
LUAD	LUAD-NYU284	KRT35	SNP	Silent	17	39633389	C	A	23	46
LUAD	LUAD-RT-S01699	KRT35	SNP	Missense_Mutation	17	39635163	G	T	33	63
LUAD	LUAD-RT-S01707	KRT35	SNP	Missense_Mutation	17	39634666	G	T	34	71
MEL	ME035	KRT35	SNP	Silent	17	39633973	G	A	47	59
MEL	MEL-JWCI-14	KRT35	SNP	Missense_Mutation	17	39635696	C	T	24	61
MEL	MEL-JWCI-WGS-25	KRT35	SNP	Missense_Mutation	17	39636937	G	A	43	74
MEL	MEL-Ma-Mel-67	KRT35	SNP	Silent	17	39635676	G	A	35	50
NB	NB-0419	KRT35	SNP	Missense_Mutation	17	39637024	G	T	42	98
LUAD	TCGA-05-4397	KRT35	SNP	Missense_Mutation	17	39636931	A	T	8	57
LUAD	TCGA-05-5420	KRT35	SNP	Missense_Mutation	17	39636983	C	A	27	53
GBM	TCGA-06-5412	KRT35	SNP	Silent	17	39637191	T	A	55	25
OV	TCGA-23-1110	KRT35	SNP	Missense_Mutation	17	39633357	T	G	60	50
GBM	TCGA-28-5211	KRT35	SNP	Silent	17	39633981	A	G	1	48
LUSC	TCGA-43-6647	KRT35	SNP	Nonsense_Mutation	17	39635146	G	T	42	52
LUAD	TCGA-44-3918	KRT35	DNP	Missense_Mutation	17	39633777	CC	AA	30	73
GBM	TCGA-76-6656	KRT35	SNP	Missense_Mutation	17	39637207	C	A	20	62
LUAD	TCGA-91-6828	KRT35	SNP	Missense_Mutation	17	39633867	G	A	38	58
BRCA	TCGA-A2-A0CS	KRT35	SNP	Silent	17	39633898	G	T	43	30
BRCA	TCGA-A8-A06U	KRT35	SNP	Missense_Mutation	17	39637093	C	T	26	80
BRCA	TCGA-A8-A095	KRT35	SNP	Silent	17	39637326	G	T	39	40
CRC	TCGA-AA-3977	KRT35	SNP	Missense_Mutation	17	39635978	T	G	64	65
CRC	TCGA-AG-A002	KRT35	SNP	Missense_Mutation	17	39635611	C	A	32	74
UCEC	TCGA-AP-A051	KRT35	SNP	Missense_Mutation	17	39635177	T	C	58	75
UCEC	TCGA-AP-A0LM	KRT35	SNP	Missense_Mutation	17	39637118	C	T	27	49
UCEC	TCGA-AP-A0LM	KRT35	SNP	Missense_Mutation	17	39637262	C	T	27	49
UCEC	TCGA-AP-A0LT	KRT35	SNP	Missense_Mutation	17	39636983	C	T	27	53
UCEC	TCGA-AX-A05Z	KRT35	SNP	Missense_Mutation	17	39634660	G	A	40	62
UCEC	TCGA-AX-A0J1	KRT35	SNP	Missense_Mutation	17	39637004	G	A	38	74
KIRC	TCGA-B0-4833	KRT35	SNP	Missense_Mutation	17	39635663	T	C	58	75
UCEC	TCGA-B5-A11E	KRT35	SNP	Missense_Mutation	17	39636967	C	T	27	73
UCEC	TCGA-B5-A11Y	KRT35	SNP	Missense_Mutation	17	39637346	C	T	26	63
KIRC	TCGA-BP-4991	KRT35	SNP	Silent	17	39635602	C	T	24	55
UCEC	TCGA-BS-A0U7	KRT35	SNP	Missense_Mutation	17	39635117	C	T	27	56
UCEC	TCGA-BS-A0UV	KRT35	SNP	Missense_Mutation	17	39635105	T	C	62	86
HNSC	TCGA-CV-6953	KRT35	SNP	Missense_Mutation	17	39635675	A	C	7	67
UCEC	TCGA-D1-A16Y	KRT35	SNP	Splice_Site	17	39635248	C	A	24	97
BLCA	TCGA-GC-A3RB	KRT35	SNP	Missense_Mutation	17	39635732	C	G	23	82