ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
HNSC	HN_62426	STK19	SNP	Missense	6	31940250	G	A	37	41
HNSC	HN_62426	STK19	SNP	Missense	6	31940454	G	C	45	59
LUAD	LUAD-F00368	STK19	SNP	Missense_Mutation	6	31948306	C	A	29	65
LUAD	LUAD-RT-S01769	STK19	SNP	Missense_Mutation	6	31940200	G	C	33	62
LUAD	LUAD-YINHD	STK19	SNP	Silent	6	31940480	G	A	45	51
MEL	ME029	STK19	SNP	Missense_Mutation	6	31940123	G	A	33	59
MEL	MEL-JWCI-WGS-1	STK19	SNP	Missense_Mutation	6	31940123	G	A	33	59
MEL	MEL-JWCI-WGS-11	STK19	SNP	Missense_Mutation	6	31940123	G	A	33	59
MEL	MEL-JWCI-WGS-31	STK19	SNP	Missense_Mutation	6	31940123	G	A	33	59
MEL	MEL-JWCI-WGS-31	STK19	SNP	Nonsense_Mutation	6	31948278	G	A	47	93
LUAD	TCGA-05-4396	STK19	SNP	Silent	6	31940167	C	A	23	46
GBM	TCGA-12-0821	STK19	INS	Frame_Shift_Ins	6	31939829	-	A	25	52
LUAD	TCGA-17-Z005	STK19	SNP	Missense_Mutation	6	31948502	C	G	23	69
LUAD	TCGA-17-Z062	STK19	SNP	Missense_Mutation	6	31940267	G	A	41	68
LUSC	TCGA-18-3414	STK19	SNP	Missense_Mutation	6	31948290	C	T	24	93
LUSC	TCGA-39-5036	STK19	SNP	Missense_Mutation	6	31948524	G	A	39	68
LUAD	TCGA-44-3919	STK19	SNP	Missense_Mutation	6	31940210	C	G	24	51
CRC	TCGA-AA-3811	STK19	SNP	Silent	6	31948549	C	T	19	50
CRC	TCGA-AA-A00N	STK19	SNP	Missense_Mutation	6	31948550	G	A	37	92
UCEC	TCGA-AX-A05Z	STK19	SNP	Missense_Mutation	6	31939805	C	A	25	74
HNSC	TCGA-BB-7864	STK19	SNP	Silent	6	31939881	C	T	21	51
BRCA	TCGA-BH-A0W5	STK19	SNP	Missense_Mutation	6	31939963	C	G	27	54
UCEC	TCGA-BS-A0UV	STK19	SNP	Missense_Mutation	6	31940177	A	C	1	49