ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
LUAD	LUAD-B00523	MAPK12	SNP	Missense_Mutation	22	50693647	G	T	39	77
MEL	ME045	MAPK12	SNP	Silent	22	50694112	G	A	34	75
MEL	MEL-Ma-Mel-67	MAPK12	SNP	Silent	22	50693783	C	T	32	62
LUSC	TCGA-34-5232	MAPK12	SNP	Splice_site	22	50694044	C	T	24	30
LUAD	TCGA-50-5044	MAPK12	DEL	Frame_Shift_Del	22	50699715	C	-	30	80
OV	TCGA-61-1919	MAPK12	SNP	Silent	22	50693771	C	T	25	50
CRC	TCGA-AA-3837	MAPK12	INS	Splice_Site	22	50696732	-	G	55	68
CRC	TCGA-AA-A01P	MAPK12	INS	Splice_Site	22	50695077	-	G	55	73
UCEC	TCGA-AP-A059	MAPK12	SNP	Missense_Mutation	22	50694561	T	C	57	89
KIRC	TCGA-B0-5698	MAPK12	SNP	Splice_Site	22	50695076	C	T	24	94
UCEC	TCGA-B5-A11N	MAPK12	SNP	Splice_Site	22	50695216	C	A	18	66
HNSC	TCGA-BB-4223	MAPK12	SNP	Missense_Mutation	22	50695547	G	C	41	64
UCEC	TCGA-D1-A103	MAPK12	SNP	Missense_Mutation	22	50694051	C	T	28	83
UCEC	TCGA-D1-A17H	MAPK12	SNP	Silent	22	50693654	G	A	40	53