ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-MEX-191	SEPT12	SNP	Nonsense_Mutation	16	4829784	G	A	39	63
CLL	CW164	SEPT12	SNP	Missense_Mutation	16	4827884	C	T	26	52
LUAD	LUAD-CHTN-Z4716A	SEPT12	SNP	Missense_Mutation	16	4837624	G	T	43	59
LUAD	LUAD-NYU284	SEPT12	SNP	Splice_site	16	4833464	C	A	23	82
MEL	ME001	SEPT12	SNP	Silent	16	4834057	G	A	41	60
MEL	ME020	SEPT12	SNP	Silent	16	4834018	C	T	24	55
MEL	ME024	SEPT12	SNP	Missense_Mutation	16	4833759	G	A	43	64
MEL	MEL-13543	SEPT12	SNP	Missense_Mutation	16	4833717	T	C	52	85
MEL	MEL-JWCI-WGS-25	SEPT12	SNP	Missense_Mutation	16	4828112	G	A	41	70
MEL	MEL-JWCI-WGS-26	SEPT12	SNP	Splice_site	16	4833765	A	C	7	85
MEL	MEL-JWCI-WGS-42	SEPT12	SNP	Splice_Site	16	4833559	C	T	32	95
MEL	MEL-Ma-Mel-114	SEPT12	SNP	Silent	16	4837638	G	A	43	51
MEL	MEL-Ma-Mel-35	SEPT12	SNP	Missense_Mutation	16	4829699	A	G	12	67
MEL	MEL-Ma-Mel-35	SEPT12	SNP	Silent	16	4833743	G	A	41	64
GBM	TCGA-06-0124	SEPT12	SNP	Missense_Mutation	16	4836007	G	A	40	95
GBM	TCGA-06-0645	SEPT12	SNP	Silent	16	4834042	G	A	40	51
LUAD	TCGA-17-Z045	SEPT12	SNP	Missense_Mutation	16	4836082	G	A	40	95
LUSC	TCGA-18-3409	SEPT12	SNP	Splice_site	16	4833651	C	T	24	52
GBM	TCGA-19-5953	SEPT12	SNP	Missense_Mutation	16	4833669	C	T	31	73
LUSC	TCGA-22-1012	SEPT12	SNP	Splice_site	16	4836106	C	A	22	95
LUSC	TCGA-22-1012	SEPT12	SNP	Splice_Site	16	4836107	C	A	24	95
LUSC	TCGA-66-2768	SEPT12	SNP	Missense_Mutation	16	4835825	C	G	32	55
LUSC	TCGA-66-2777	SEPT12	SNP	Missense_Mutation	16	4827908	G	A	39	63
LUAD	TCGA-86-6562	SEPT12	SNP	Nonsense_Mutation	16	4829784	G	A	39	63
BRCA	TCGA-A2-A25D	SEPT12	SNP	Missense_Mutation	16	4835875	C	T	22	82
CRC	TCGA-AA-3821	SEPT12	SNP	Splice_site	16	4833464	C	T	23	82
CRC	TCGA-AA-A00J	SEPT12	SNP	Silent	16	4829784	G	T	39	63
CRC	TCGA-AA-A017	SEPT12	SNP	Silent	16	4835843	C	T	27	37
CRC	TCGA-AA-A01R	SEPT12	SNP	Splice_site	16	4828088	G	A	39	78
CRC	TCGA-AG-3586	SEPT12	SNP	Silent	16	4836036	T	A	59	42
BRCA	TCGA-AN-A049	SEPT12	SNP	Missense_Mutation	16	4829718	G	A	39	62
UCEC	TCGA-AP-A051	SEPT12	SNP	Missense_Mutation	16	4835828	G	C	44	67
UCEC	TCGA-B5-A0JY	SEPT12	SNP	Missense_Mutation	16	4827986	C	A	32	81
HNSC	TCGA-BA-4074	SEPT12	SNP	Missense_Mutation	16	4833975	G	A	39	76
HNSC	TCGA-BA-5149	SEPT12	SNP	Missense_Mutation	16	4835848	C	G	30	95
UCEC	TCGA-BG-A0W2	SEPT12	SNP	Missense_Mutation	16	4829717	C	T	23	96
UCEC	TCGA-BS-A0UF	SEPT12	SNP	Missense_Mutation	16	4835879	C	A	32	67
HNSC	TCGA-CR-6481	SEPT12	SNP	Nonsense_Mutation	16	4835884	C	A	32	82
UCEC	TCGA-D1-A101	SEPT12	SNP	Silent	16	4828125	C	T	27	38
UCEC	TCGA-D1-A17Q	SEPT12	SNP	Missense_Mutation	16	4834056	G	T	35	52
BRCA	TCGA-D8-A1X8	SEPT12	SNP	Silent	16	4829725	G	A	41	51
KIRC	TCGA-EU-5904	SEPT12	SNP	Nonsense_Mutation	16	4833399	T	A	64	69