ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
HNSC	HN_63058	RAC1	SNP	Missense	7	6426892	C	T	30	100
MEL	ME011	RAC1	SNP	Silent	7	6431666	G	A	38	47
MEL	ME017	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
MEL	MEL-JWCI-14	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
MEL	MEL-JWCI-WGS-7	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
MEL	MEL-Ma-Mel-85	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
MEL	MEL-UKRV-Mel-20	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
MM	MM-0527	RAC1	SNP	Missense_Mutation	7	6439807	T	A	51	61
LUSC	TCGA-34-5927	RAC1	SNP	Missense_Mutation	7	6431584	T	G	57	92
KIRC	TCGA-A3-3317	RAC1	SNP	Silent	7	6442071	G	C	48	54
UCEC	TCGA-AP-A056	RAC1	SNP	Missense_Mutation	7	6426880	A	G	2	93
UCEC	TCGA-AP-A059	RAC1	SNP	Silent	7	6441972	G	A	39	25
HNSC	TCGA-BA-4078	RAC1	SNP	Missense_Mutation	7	6441558	A	C	2	51
KIRC	TCGA-BP-4342	RAC1	SNP	Missense_Mutation	7	6431566	A	C	16	92
UCEC	TCGA-BS-A0UF	RAC1	SNP	Silent	7	6438343	G	A	37	50
HNSC	TCGA-CN-5369	RAC1	SNP	Missense_Mutation	7	6441974	C	T	27	100
HNSC	TCGA-CQ-6223	RAC1	SNP	Missense_Mutation	7	6426850	G	A	35	100
HNSC	TCGA-CR-5250	RAC1	SNP	Missense_Mutation	7	6426860	G	T	46	100
HNSC	TCGA-CR-7367	RAC1	SNP	Missense_Mutation	7	6441634	G	A	43	100
HNSC	TCGA-CR-7388	RAC1	SNP	Missense_Mutation	7	6441557	A	G	1	93
HNSC	TCGA-CV-7427	RAC1	SNP	Missense_Mutation	7	6426892	C	A	30	100
HNSC	TCGA-CX-7085	RAC1	SNP	Missense_Mutation	7	6431563	A	G	4	79
HNSC	TCGA-CX-7085	RAC1	SNP	Missense_Mutation	7	6441974	C	T	27	100
UCEC	TCGA-EY-A1GS	RAC1	SNP	Missense_Mutation	7	6426892	C	T	30	100
BLCA	TCGA-GD-A3OP	RAC1	SNP	Missense_Mutation	7	6431604	C	G	32	77
HNSC	TCGA-H7-7774	RAC1	SNP	Missense_Mutation	7	6426860	G	A	46	100