ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-175	MYCN	SNP	Missense_Mutation	2	16086160	A	C	1	63
LUAD	LUAD-CHTN-MAD06-00668	MYCN	SNP	Missense_Mutation	2	16086147	G	C	46	71
MEL	ME045	MYCN	SNP	Missense_Mutation	2	16085897	C	T	23	71
MEL	ME049	MYCN	SNP	Missense_Mutation	2	16085956	G	A	41	98
MEL	MEL-JWCI-WGS-3	MYCN	SNP	Missense_Mutation	2	16085834	C	T	22	99
MEL	MEL-JWCI-WGS-34	MYCN	SNP	Missense_Mutation	2	16086052	G	A	41	100
MEL	MEL-JWCI-WGS-7	MYCN	SNP	Silent	2	16085670	G	A	47	63
MEL	MEL-Ma-Mel-119	MYCN	SNP	Silent	2	16085802	C	T	30	73
PRAD	PR-0415	MYCN	SNP	Missense_Mutation	2	16082482	T	C	55	55
OV	TCGA-09-0369	MYCN	SNP	Missense_Mutation	2	16085897	C	T	23	71
LUAD	TCGA-17-Z022	MYCN	SNP	Nonsense_Mutation	2	16082254	C	A	31	70
LUSC	TCGA-18-3409	MYCN	SNP	Silent	2	16082519	C	T	30	51
GBM	TCGA-26-5136	MYCN	SNP	Missense_Mutation	2	16082359	C	T	19	92
OV	TCGA-36-1568	MYCN	SNP	Synonymous	2	16082408	C	G	22	51
LUAD	TCGA-38-4631	MYCN	SNP	Silent	2	16085778	G	T	45	58
LUAD	TCGA-49-6767	MYCN	SNP	Missense_Mutation	2	16082194	G	T	34	52
LUSC	TCGA-60-2698	MYCN	SNP	Silent	2	16086030	C	T	29	53
LUSC	TCGA-60-2726	MYCN	SNP	Silent	2	16082411	G	T	37	58
LUSC	TCGA-85-6560	MYCN	SNP	Missense_Mutation	2	16082189	G	A	46	59
UCEC	TCGA-A5-A0GQ	MYCN	SNP	Missense_Mutation	2	16082317	C	T	22	92
CRC	TCGA-AA-3811	MYCN	SNP	Missense_Mutation	2	16085893	C	T	19	69
CRC	TCGA-AG-A002	MYCN	SNP	Missense_Mutation	2	16082286	G	T	45	88
CRC	TCGA-AG-A002	MYCN	SNP	Missense_Mutation	2	16085942	G	A	37	99
UCEC	TCGA-AP-A059	MYCN	SNP	Silent	2	16085655	C	T	31	47
UCEC	TCGA-AP-A0LV	MYCN	SNP	Missense_Mutation	2	16085981	A	G	6	91
UCEC	TCGA-AX-A064	MYCN	SNP	Missense_Mutation	2	16082317	C	T	22	92
UCEC	TCGA-B5-A11E	MYCN	SNP	Missense_Mutation	2	16085786	A	G	1	68
BRCA	TCGA-B6-A0I8	MYCN	SNP	Missense_Mutation	2	16086025	T	A	56	91
UCEC	TCGA-BG-A0MQ	MYCN	SNP	Missense_Mutation	2	16082317	C	T	22	92
BRCA	TCGA-BH-A18P	MYCN	SNP	Splice_site	2	16082186	G	A	37	51
KIRC	TCGA-BP-5185	MYCN	SNP	Missense_Mutation	2	16085629	G	A	45	97
BLCA	TCGA-BT-A2LB	MYCN	SNP	Silent	2	16082291	C	T	32	65
HNSC	TCGA-CV-6941	MYCN	SNP	Missense_Mutation	2	16085953	T	A	54	91
HNSC	TCGA-CV-7425	MYCN	SNP	Missense_Mutation	2	16086016	C	T	31	64
UCEC	TCGA-D1-A15W	MYCN	SNP	Missense_Mutation	2	16082317	C	T	22	92
UCEC	TCGA-D1-A160	MYCN	SNP	Missense_Mutation	2	16085981	A	G	6	91
BLCA	TCGA-DK-A1AC	MYCN	SNP	Splice_site	2	16082186	G	A	37	51
BLCA	TCGA-DK-A2I4	MYCN	SNP	Silent	2	16085691	C	T	21	53
HNSC	TCGA-DQ-7589	MYCN	SNP	Missense_Mutation	2	16086155	A	T	3	91
BLCA	TCGA-G2-A2EO	MYCN	SNP	Missense_Mutation	2	16082244	G	C	37	93