ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
CLL	CW117	EIF2S2	SNP	Missense_Mutation	20	32677564	C	T	31	100
HNSC	HN_00313	EIF2S2	SNP	Missense	20	32681530	G	A	37	100
GBM	TCGA-06-2562	EIF2S2	SNP	Missense_Mutation	20	32677582	T	C	55	94
LUSC	TCGA-60-2698	EIF2S2	SNP	Missense_Mutation	20	32677584	G	T	41	90
CRC	TCGA-AA-A010	EIF2S2	SNP	Nonsense_Mutation	20	32693249	C	A	32	95
UCEC	TCGA-AP-A059	EIF2S2	SNP	Splice_Site	20	32693352	C	A	32	96
UCEC	TCGA-AX-A05Z	EIF2S2	SNP	Missense_Mutation	20	32684501	C	A	32	79
UCEC	TCGA-AX-A0J0	EIF2S2	SNP	Splice_Site	20	32693352	C	A	32	96
UCEC	TCGA-B5-A0JY	EIF2S2	SNP	Missense_Mutation	20	32684576	C	A	32	68
UCEC	TCGA-B5-A11N	EIF2S2	SNP	Missense_Mutation	20	32684576	C	A	32	68
HNSC	TCGA-BB-7863	EIF2S2	DEL	In_Frame_Del	20	32677659	CTT	-	24	89
UCEC	TCGA-BG-A187	EIF2S2	SNP	Missense_Mutation	20	32677652	G	C	40	79
BRCA	TCGA-BH-A0HP	EIF2S2	SNP	Missense_Mutation	20	32685285	G	C	33	56
KIRC	TCGA-BP-5180	EIF2S2	SNP	Splice_site	20	32699916	T	A	51	79
UCEC	TCGA-BS-A0UF	EIF2S2	SNP	Nonsense_Mutation	20	32684602	G	A	37	58
UCEC	TCGA-BS-A0UJ	EIF2S2	SNP	Missense_Mutation	20	32684509	C	T	24	100
HNSC	TCGA-CV-6959	EIF2S2	DEL	Splice_site	20	32693175	T	-	56	62
HNSC	TCGA-CV-7414	EIF2S2	SNP	Missense_Mutation	20	32677564	C	T	31	100
UCEC	TCGA-D1-A16Y	EIF2S2	SNP	Missense_Mutation	20	32681530	G	A	37	100
BRCA	TCGA-EW-A1J2	EIF2S2	SNP	Missense_Mutation	20	32678367	C	T	32	99