ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
CLL	CW194	SFRS2	SNP	Missense_Mutation	17	74732921	G	T	39	77
DLBCL	DLBCL-LS4592	SFRS2	SNP	Missense_Mutation	17	74732968	T	G	57	68
DLBCL	DLBCL-Ls2596	SFRS2	SNP	Silent	17	74732973	C	T	27	54
LUAD	LUAD-D02185	SFRS2	SNP	Silent	17	74732492	G	A	46	49
LUAD	LUAD-YINHD	SFRS2	SNP	Missense_Mutation	17	74732542	T	A	53	59
LUAD	TCGA-05-4403	SFRS2	SNP	Silent	17	74733003	C	G	21	52
GBM	TCGA-06-0189	SFRS2	SNP	Missense_Mutation	17	74732284	G	T	41	71
LUSC	TCGA-37-4133	SFRS2	SNP	Missense_Mutation	17	74732326	C	G	20	59
LUSC	TCGA-66-2773	SFRS2	SNP	Missense_Mutation	17	74732373	G	C	33	89
LUSC	TCGA-66-2773	SFRS2	SNP	Silent	17	74733066	G	A	37	70
AML	TCGA-AB-2805	SFRS2	SNP	Missense_Mutation	17	74732959	G	A	43	75
AML	TCGA-AB-2810	SFRS2	SNP	Missense_Mutation	17	74732959	G	T	43	75
AML	TCGA-AB-2850	SFRS2	DEL	In_Frame_Del	17	74732936	GGCGGCTGTGGTGTGAGTCCGGGG	-	39	55
AML	TCGA-AB-2959	SFRS2	SNP	Missense_Mutation	17	74732959	G	A	43	75
CRC	TCGA-AG-A002	SFRS2	SNP	Missense_Mutation	17	74732349	G	T	33	83
BRCA	TCGA-BH-A1EV	SFRS2	SNP	Missense_Mutation	17	74732502	G	C	41	84
KIRC	TCGA-BP-4167	SFRS2	SNP	Silent	17	74732441	T	C	50	43
BLCA	TCGA-BT-A3PJ	SFRS2	SNP	Missense_Mutation	17	74732409	C	T	31	76
HNSC	TCGA-CV-6962	SFRS2	SNP	Missense_Mutation	17	74732524	G	C	39	59
KIRC	TCGA-CZ-5457	SFRS2	SNP	Nonsense_Mutation	17	74732524	G	A	39	59
UCEC	TCGA-D1-A0ZN	SFRS2	SNP	Missense_Mutation	17	74733188	C	T	30	96
HNSC	TCGA-D6-6516	SFRS2	SNP	Missense_Mutation	17	74732409	C	A	31	76
BLCA	TCGA-FD-A3B5	SFRS2	SNP	Missense_Mutation	17	74732295	C	A	31	71
BLCA	TCGA-G2-A2EO	SFRS2	SNP	Missense_Mutation	17	74732523	C	A	31	75