ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0014	MAPK1	SNP	Missense_Mutation	22	22160188	C	A	19	99
CLL	CLL-JJ	MAPK1	SNP	Missense_Mutation	22	22160147	C	T	29	99
CLL	CLL_080	MAPK1	SNP	Missense_Mutation	22	22127181	T	A	49	91
CLL	CLL_080	MAPK1	SNP	Missense_Mutation	22	22127256	T	C	58	78
MEL	MEL-JWCI-WGS-1	MAPK1	SNP	Missense_Mutation	22	22160210	G	A	47	99
GBM	TCGA-06-2559	MAPK1	SNP	Missense_Mutation	22	22142672	G	A	33	80
LUSC	TCGA-22-1002	MAPK1	SNP	Missense_Mutation	22	22160146	T	C	50	90
OV	TCGA-24-1553	MAPK1	SNP	Silent	22	22160202	A	T	15	51
LUSC	TCGA-39-5031	MAPK1	SNP	Silent	22	22160160	G	T	45	63
GBM	TCGA-76-4928	MAPK1	SNP	Missense_Mutation	22	22142632	T	C	52	94
CRC	TCGA-AA-3870	MAPK1	SNP	Missense_Mutation	22	22162101	C	A	28	98
CRC	TCGA-AA-A010	MAPK1	SNP	Missense_Mutation	22	22142617	T	G	60	94
AML	TCGA-AB-2971	MAPK1	SNP	Missense_Mutation	22	22153395	C	T	19	100
UCEC	TCGA-AP-A051	MAPK1	SNP	Missense_Mutation	22	22160270	G	T	35	84
UCEC	TCGA-AX-A05Z	MAPK1	SNP	Nonsense_Mutation	22	22123543	C	A	32	100
KIRC	TCGA-B0-4841	MAPK1	SNP	Silent	22	22142570	G	A	34	74
BRCA	TCGA-BH-A0B5	MAPK1	SNP	Missense_Mutation	22	22162014	C	T	29	98
HNSC	TCGA-CQ-5334	MAPK1	SNP	Missense_Mutation	22	22127164	C	T	31	99
HNSC	TCGA-CV-5442	MAPK1	SNP	Missense_Mutation	22	22127164	C	T	31	99
HNSC	TCGA-CV-5971	MAPK1	SNP	Missense_Mutation	22	22127164	C	T	31	99
HNSC	TCGA-CV-7261	MAPK1	SNP	Nonsense_Mutation	22	22127164	C	A	31	99
BLCA	TCGA-DK-A1A3	MAPK1	SNP	Silent	22	22161970	G	A	37	52