ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
HNSC	HN_00076	RRAS2	SNP	Missense	11	14380346	C	T	26	84
LUAD	LUAD-NYU847	RRAS2	SNP	Silent	11	14380330	C	A	27	58
LUAD	LUAD-RT-S01707	RRAS2	SNP	Missense_Mutation	11	14303157	C	T	23	100
MEL	MEL-JWCI-WGS-13	RRAS2	SNP	Silent	11	14303171	G	A	41	69
LUSC	TCGA-37-4141	RRAS2	DEL	Frame_Shift_Del	11	14380349	C	-	26	72
LUSC	TCGA-43-6771	RRAS2	SNP	Missense_Mutation	11	14316390	T	A	63	92
LUAD	TCGA-49-4505	RRAS2	SNP	Missense_Mutation	11	14316111	T	C	49	60
CRC	TCGA-AA-3984	RRAS2	SNP	Missense_Mutation	11	14316076	G	A	37	66
CRC	TCGA-AG-A002	RRAS2	SNP	Missense_Mutation	11	14317365	C	A	32	94
UCEC	TCGA-AX-A05Z	RRAS2	SNP	Silent	11	14316023	T	C	64	48
UCEC	TCGA-B5-A0K4	RRAS2	SNP	Missense_Mutation	11	14316389	T	A	56	79
UCEC	TCGA-BG-A0M4	RRAS2	SNP	Missense_Mutation	11	14316390	T	A	63	92
UCEC	TCGA-BG-A0YU	RRAS2	SNP	Missense_Mutation	11	14316389	T	G	56	79
HNSC	TCGA-CV-7430	RRAS2	SNP	Missense_Mutation	11	14316390	T	A	63	92
UCEC	TCGA-D1-A17U	RRAS2	SNP	Missense_Mutation	11	14303235	C	T	23	100
CARC	Carc-DFCI-184	RRAS2	SNP	Splice_Site	11	14316304	A	C	2	69