ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-MEX-191	LGMN	SNP	Silent	14	93180775	G	A	45	52
MEL	MEL-JWCI-14	LGMN	SNP	Missense_Mutation	14	93183732	G	A	36	69
MEL	MEL-Ma-Mel-65	LGMN	SNP	Silent	14	93182546	G	A	41	60
MEL	MEL-Ma-Mel-67	LGMN	SNP	Silent	14	93172963	G	A	37	41
MM	MM-0545	LGMN	SNP	Missense_Mutation	14	93178231	G	A	40	98
LUAD	TCGA-05-4396	LGMN	SNP	Missense_Mutation	14	93170994	G	T	39	70
LUAD	TCGA-05-4396	LGMN	SNP	Nonsense_Mutation	14	93171049	C	A	31	93
LUAD	TCGA-44-3919	LGMN	SNP	Missense_Mutation	14	93183754	G	C	45	43
LUAD	TCGA-50-6590	LGMN	SNP	Splice_Site	14	93183807	C	A	28	98
LUAD	TCGA-91-6828	LGMN	SNP	Missense_Mutation	14	93199091	C	A	26	53
UCEC	TCGA-A5-A0GA	LGMN	SNP	Missense_Mutation	14	93178208	C	T	19	98
CRC	TCGA-A6-2676	LGMN	SNP	Nonsense_Mutation	14	93180173	G	A	39	58
CRC	TCGA-AA-3672	LGMN	SNP	Silent	14	93178266	C	T	19	20
CRC	TCGA-AA-3864	LGMN	SNP	Silent	14	93172963	G	A	37	41
CRC	TCGA-AG-3578	LGMN	SNP	Splice_site	14	93172829	G	A	40	50
CRC	TCGA-AG-A002	LGMN	SNP	Missense_Mutation	14	93170702	T	G	64	56
UCEC	TCGA-AP-A056	LGMN	SNP	Missense_Mutation	14	93180774	T	C	51	52
UCEC	TCGA-AP-A059	LGMN	SNP	Missense_Mutation	14	93176117	C	T	28	94
UCEC	TCGA-AP-A059	LGMN	SNP	Splice_Site	14	93179217	C	A	32	100
UCEC	TCGA-AX-A05S	LGMN	SNP	Missense_Mutation	14	93178024	C	T	19	100
UCEC	TCGA-B5-A0JY	LGMN	SNP	Missense_Mutation	14	93185138	C	T	31	100
UCEC	TCGA-B5-A11E	LGMN	SNP	Splice_Site	14	93179217	C	A	32	100
UCEC	TCGA-BS-A0TG	LGMN	SNP	Missense_Mutation	14	93176130	C	A	29	95
HNSC	TCGA-CR-5243	LGMN	SNP	Missense_Mutation	14	93182496	C	T	26	97
HNSC	TCGA-CR-7383	LGMN	SNP	Silent	14	93176022	G	A	33	91
HNSC	TCGA-CV-6436	LGMN	SNP	Missense_Mutation	14	93172970	C	T	19	30
HNSC	TCGA-CV-7099	LGMN	SNP	Silent	14	93199105	G	A	45	51
HNSC	TCGA-HL-7533	LGMN	SNP	Splice_Site	14	93179217	C	T	32	100