ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-MEX-045	GNB1	SNP	Synonymous	1	1721924	A	C	3	61
CLL	CLL_024	GNB1	SNP	Missense_Mutation	1	1737942	A	G	12	78
CLL	CW113	GNB1	SNP	Missense_Mutation	1	1737942	A	G	12	78
DLBCL	DLBCL-LS4618	GNB1	SNP	Missense_Mutation	1	1747199	A	T	11	91
DLBCL	DLBCL-Ls3387	GNB1	SNP	Missense_Mutation	1	1737942	A	T	12	78
LUAD	LUAD-5V8LT	GNB1	SNP	Missense_Mutation	1	1720498	G	C	39	57
LUAD	LUAD-RT-S01702	GNB1	SNP	Silent	1	1735946	G	A	38	40
LUAD	LUAD-RT-S01770	GNB1	SNP	Missense_Mutation	1	1721844	T	C	52	77
LUAD	LUAD-RT-S01831	GNB1	SNP	Missense_Mutation	1	1720594	C	T	23	98
MEL	MEL-Ma-Mel-48	GNB1	SNP	Silent	1	1747287	G	A	37	46
PRAD	PR-P559	GNB1	SNP	Silent	1	1724728	G	A	41	74
LUAD	TCGA-05-4396	GNB1	SNP	Splice_site	1	1756837	C	A	31	92
LUAD	TCGA-17-Z042	GNB1	SNP	Splice_Site	1	1721833	C	G	19	98
GBM	TCGA-32-2495	GNB1	SNP	Missense_Mutation	1	1720568	C	A	32	99
LUSC	TCGA-85-6561	GNB1	SNP	Splice_site	1	1756837	C	A	31	92
CRC	TCGA-AA-3845	GNB1	SNP	Missense_Mutation	1	1718847	T	C	55	77
CRC	TCGA-AA-3947	GNB1	SNP	Silent	1	1721912	T	C	55	43
CRC	TCGA-AA-A00N	GNB1	SNP	Silent	1	1721936	G	A	37	56
AML	TCGA-AB-2805	GNB1	SNP	Missense_Mutation	1	1747228	T	G	56	91
KIRC	TCGA-AK-3444	GNB1	SNP	Missense_Mutation	1	1721888	T	G	56	59
UCEC	TCGA-AP-A051	GNB1	SNP	Missense_Mutation	1	1720561	G	A	38	85
UCEC	TCGA-AP-A059	GNB1	SNP	Silent	1	1720667	G	A	40	42
UCEC	TCGA-AP-A0LM	GNB1	SNP	Silent	1	1737959	C	T	27	44
UCEC	TCGA-AX-A05S	GNB1	SNP	Missense_Mutation	1	1735936	C	A	30	98
HNSC	TCGA-BA-5152	GNB1	SNP	Missense_Mutation	1	1721851	C	T	29	99
BRCA	TCGA-BH-A0HN	GNB1	SNP	Missense_Mutation	1	1720602	A	G	12	90
KIRC	TCGA-BP-4993	GNB1	SNP	Missense_Mutation	1	1749311	C	A	27	96
HNSC	TCGA-CV-6953	GNB1	SNP	Missense_Mutation	1	1720641	C	T	19	85
BLCA	TCGA-DK-A1AC	GNB1	SNP	Missense_Mutation	1	1720630	C	T	30	98
BLCA	TCGA-DK-A1AC	GNB1	SNP	Missense_Mutation	1	1720636	C	T	29	85
BLCA	TCGA-DK-A3IU	GNB1	SNP	Missense_Mutation	1	1749278	G	T	45	96
BLCA	TCGA-E5-A2PC	GNB1	SNP	Missense_Mutation	1	1756890	C	A	29	92
BLCA	TCGA-G2-A2ES	GNB1	SNP	Missense_Mutation	1	1721920	C	T	29	99