ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-0019	HRAS	SNP	Nonsense_Mutation	11	534227	G	C	40	46
HNSC	HN_00466	HRAS	SNP	Missense	11	533875	G	T	47	92
HNSC	HN_62469	HRAS	SNP	Missense	11	534285	C	A	18	91
HNSC	HN_62863	HRAS	SNP	Missense	11	534288	C	G	26	91
HNSC	HN_63080	HRAS	SNP	Missense	11	534288	C	T	26	91
LUAD	LUAD-2GUGK	HRAS	SNP	Missense_Mutation	11	534286	C	G	23	91
MEL	MEL-Ma-Mel-48	HRAS	DNP	Missense_Mutation	11	534285	CC	AT	18	91
LUAD	TCGA-05-4420	HRAS	SNP	Missense_Mutation	11	533874	T	A	55	85
LUSC	TCGA-18-3414	HRAS	SNP	Missense_Mutation	11	534286	C	A	23	91
LUSC	TCGA-21-5786	HRAS	SNP	Missense_Mutation	11	533874	T	C	55	85
LUSC	TCGA-34-2600	HRAS	SNP	Missense_Mutation	11	533875	G	T	47	92
LUSC	TCGA-34-2600	HRAS	SNP	Missense_Mutation	11	534283	C	A	17	91
LUSC	TCGA-34-5240	HRAS	SNP	Missense_Mutation	11	534286	C	G	23	91
LUSC	TCGA-66-2758	HRAS	SNP	Missense_Mutation	11	534285	C	A	18	91
BRCA	TCGA-A2-A0D0	HRAS	SNP	Silent	11	534227	G	A	40	46
HNSC	TCGA-BA-5556	HRAS	SNP	Missense_Mutation	11	534286	C	G	23	91
BLCA	TCGA-BT-A2LB	HRAS	SNP	Missense_Mutation	11	534226	C	T	31	91
BLCA	TCGA-CF-A3MI	HRAS	SNP	Missense_Mutation	11	534286	C	G	23	91
KIRC	TCGA-CJ-4874	HRAS	SNP	Missense_Mutation	11	533545	G	C	35	81
HNSC	TCGA-CQ-5324	HRAS	SNP	Missense_Mutation	11	534285	C	A	18	91
HNSC	TCGA-CQ-5324	HRAS	SNP	Missense_Mutation	11	534291	G	T	42	91
HNSC	TCGA-CQ-7068	HRAS	SNP	Missense_Mutation	11	534285	C	A	18	91
HNSC	TCGA-CR-7382	HRAS	SNP	Missense_Mutation	11	534289	C	T	23	91
HNSC	TCGA-CR-7394	HRAS	SNP	Missense_Mutation	11	534289	C	T	23	91
HNSC	TCGA-CR-7395	HRAS	SNP	Missense_Mutation	11	534288	C	T	26	91
HNSC	TCGA-CV-6436	HRAS	SNP	Missense_Mutation	11	534288	C	T	26	91
HNSC	TCGA-CV-6938	HRAS	SNP	Missense_Mutation	11	534288	C	G	26	91
HNSC	TCGA-CV-7183	HRAS	SNP	Missense_Mutation	11	534289	C	A	23	91
HNSC	TCGA-CV-7250	HRAS	SNP	Missense_Mutation	11	533874	T	A	55	85
UCEC	TCGA-D1-A167	HRAS	SNP	Missense_Mutation	11	533881	C	T	27	92
BLCA	TCGA-DK-A1AC	HRAS	SNP	Missense_Mutation	11	533785	C	T	29	92
BLCA	TCGA-G2-A2EJ	HRAS	SNP	Missense_Mutation	11	534288	C	T	26	91
BLCA	TCGA-GD-A3OQ	HRAS	SNP	Missense_Mutation	11	534288	C	T	26	91
HNSC	TCGA-IQ-7631	HRAS	SNP	Missense_Mutation	11	534285	C	A	18	91