ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
LUAD	LUAD-CHTN-Z4716A	MIER3	SNP	Missense_Mutation	5	56229084	T	A	58	89
LUAD	LUAD-F00089	MIER3	SNP	Nonsense_Mutation	5	56242794	C	A	29	98
LUAD	TCGA-17-Z022	MIER3	SNP	Missense_Mutation	5	56229127	C	T	29	97
LUSC	TCGA-18-3408	MIER3	SNP	Missense_Mutation	5	56219584	G	C	39	67
LUSC	TCGA-34-2600	MIER3	SNP	Missense_Mutation	5	56233465	C	T	29	100
CRC	TCGA-A6-2672	MIER3	SNP	Missense_Mutation	5	56229132	C	T	26	82
CRC	TCGA-AA-3526	MIER3	SNP	Nonsense_Mutation	5	56233408	G	A	40	64
CRC	TCGA-AA-3555	MIER3	SNP	Missense_Mutation	5	56226524	C	T	31	84
CRC	TCGA-AA-3672	MIER3	DEL	Frame_Shift_Del	5	56219767	T	-	56	61
CRC	TCGA-AA-3715	MIER3	SNP	Splice_site	5	56219742	G	A	40	99
CRC	TCGA-AA-3864	MIER3	DEL	In_Frame_Del	5	56219756	ATGGTT	-	12	60
CRC	TCGA-AA-3977	MIER3	SNP	Nonsense_Mutation	5	56234736	C	A	29	87
CRC	TCGA-AA-3984	MIER3	SNP	Missense_Mutation	5	56219166	C	A	32	98
CRC	TCGA-AA-A010	MIER3	SNP	Missense_Mutation	5	56242838	T	G	58	90
CRC	TCGA-AA-A022	MIER3	SNP	Missense_Mutation	5	56234723	A	G	8	79
AML	TCGA-AB-3006	MIER3	SNP	Missense_Mutation	5	56224656	G	C	39	70
CRC	TCGA-AG-A002	MIER3	SNP	Missense_Mutation	5	56229214	C	T	31	97
UCEC	TCGA-AP-A0LM	MIER3	SNP	Missense_Mutation	5	56229110	C	A	30	52
UCEC	TCGA-AP-A0LM	MIER3	SNP	Silent	5	56231271	G	A	40	51
UCEC	TCGA-AX-A05Z	MIER3	SNP	Missense_Mutation	5	56233420	G	A	43	88
UCEC	TCGA-AX-A060	MIER3	SNP	Missense_Mutation	5	56224613	T	C	51	88
BLCA	TCGA-BT-A20J	MIER3	SNP	Missense_Mutation	5	56219227	A	T	13	90
HNSC	TCGA-CV-6955	MIER3	SNP	Missense_Mutation	5	56234739	C	G	32	87