ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-0950	RHOA	SNP	Missense_Mutation	3	49397673	C	T	22	100
HNSC	HN_00313	RHOA	SNP	Missense	3	49412905	C	G	29	100
HNSC	HN_62756	RHOA	DNP	Missense	3	49412898	TA	AT	49	91
LUAD	LUAD-CHTN-MAD08-00104	RHOA	SNP	Silent	3	49405928	C	T	26	50
MEL	MEL-JWCI-WGS-22	RHOA	SNP	Missense_Mutation	3	49405884	G	A	41	99
MEL	MEL-Ma-Mel-114	RHOA	SNP	Missense_Mutation	3	49405915	G	A	43	99
OV	TCGA-04-1350	RHOA	SNP	Missense_Mutation	3	49412973	C	A	30	100
OV	TCGA-10-0933	RHOA	SNP	Missense_Mutation	3	49405912	C	T	32	99
LUAD	TCGA-50-5051	RHOA	SNP	Missense_Mutation	3	49399951	C	A	23	100
BRCA	TCGA-A8-A09G	RHOA	SNP	Missense_Mutation	3	49412905	C	G	29	100
CRC	TCGA-AA-3845	RHOA	SNP	Missense_Mutation	3	49405956	G	A	34	99
CRC	TCGA-AA-3972	RHOA	INS	Frame_Shift_Ins	3	49405884	-	A	41	99
CRC	TCGA-AA-A01P	RHOA	SNP	Missense_Mutation	3	49405932	A	G	7	91
CRC	TCGA-AA-A01R	RHOA	SNP	Missense_Mutation	3	49413009	C	T	23	100
CRC	TCGA-AG-3892	RHOA	SNP	Missense_Mutation	3	49397763	A	C	1	78
UCEC	TCGA-AP-A051	RHOA	SNP	Missense_Mutation	3	49412953	C	A	20	100
UCEC	TCGA-B5-A11N	RHOA	SNP	Missense_Mutation	3	49397782	C	T	26	100
UCEC	TCGA-B5-A11U	RHOA	SNP	Missense_Mutation	3	49397700	G	A	40	100
BRCA	TCGA-BH-A0E0	RHOA	SNP	Missense_Mutation	3	49413010	G	A	39	52
BLCA	TCGA-BT-A2LD	RHOA	SNP	Missense_Mutation	3	49412958	A	G	11	91
HNSC	TCGA-CN-6998	RHOA	SNP	Missense_Mutation	3	49412905	C	G	29	100
HNSC	TCGA-CV-7102	RHOA	SNP	Missense_Mutation	3	49412905	C	G	29	100
HNSC	TCGA-CV-7410	RHOA	SNP	Missense_Mutation	3	49412905	C	G	29	100
BLCA	TCGA-DK-A2I1	RHOA	SNP	Missense_Mutation	3	49405951	G	T	46	99
HNSC	TCGA-DQ-5625	RHOA	SNP	Missense_Mutation	3	49412905	C	G	29	100
BLCA	TCGA-G2-A2EK	RHOA	SNP	Missense_Mutation	3	49397710	C	T	29	100
BLCA	TCGA-H4-A2HQ	RHOA	SNP	Missense_Mutation	3	49400019	G	C	33	87