ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
ESO	ESO-153	PDCD2L	SNP	Missense_Mutation	19	34904667	T	A	49	78
HNSC	HN_63048	PDCD2L	SNP	Missense	19	34912537	C	T	21	89
LUAD	LUAD-E01278	PDCD2L	SNP	Missense_Mutation	19	34900387	A	G	8	39
LUAD	LUAD-S01346	PDCD2L	SNP	Missense_Mutation	19	34895651	C	T	30	79
MEL	ME009	PDCD2L	SNP	Missense_Mutation	19	34895705	C	T	18	48
MEL	MEL-JWCI-WGS-7	PDCD2L	SNP	Silent	19	34900254	C	T	22	50
MEL	MEL-Ma-Mel-122	PDCD2L	SNP	Missense_Mutation	19	34900121	G	T	41	81
MM	MM-0464	PDCD2L	SNP	Missense_Mutation	19	34895579	C	T	22	75
OV	TCGA-23-1120	PDCD2L	SNP	Missense	19	34900109	C	A	28	81
OV	TCGA-24-1422	PDCD2L	SNP	Missense_Mutation	19	34900210	C	G	31	62
LUSC	TCGA-66-2766	PDCD2L	SNP	Missense_Mutation	19	34895654	C	G	23	67
GBM	TCGA-81-5910	PDCD2L	SNP	Silent	19	34895691	C	T	26	51
CRC	TCGA-AA-3558	PDCD2L	SNP	Missense_Mutation	19	34900388	T	C	52	76
CRC	TCGA-AA-A00J	PDCD2L	SNP	Silent	19	34916905	G	A	47	49
AML	TCGA-AB-2874	PDCD2L	SNP	Missense_Mutation	19	34904746	T	C	52	78
AML	TCGA-AB-2891	PDCD2L	SNP	Missense_Mutation	19	34900370	A	G	16	76
CRC	TCGA-AG-3581	PDCD2L	SNP	Silent	19	34900368	C	T	20	48
CRC	TCGA-AG-3902	PDCD2L	SNP	Silent	19	34916980	A	G	4	52
UCEC	TCGA-AX-A05Z	PDCD2L	SNP	Nonsense_Mutation	19	34900381	G	T	33	81
BRCA	TCGA-B6-A0I8	PDCD2L	SNP	Silent	19	34900086	A	C	7	46
KIRC	TCGA-BP-4803	PDCD2L	SNP	Missense_Mutation	19	34900211	G	T	39	55
UCEC	TCGA-BS-A0UF	PDCD2L	SNP	Nonsense_Mutation	19	34916906	G	T	41	87
HNSC	TCGA-CN-5369	PDCD2L	SNP	Nonsense_Mutation	19	34912527	C	T	29	89
HNSC	TCGA-CN-5374	PDCD2L	SNP	Missense_Mutation	19	34912449	T	A	56	82
HNSC	TCGA-CR-6472	PDCD2L	SNP	Missense_Mutation	19	34904736	C	G	29	84
HNSC	TCGA-CR-6484	PDCD2L	SNP	Silent	19	34912556	C	G	29	51
HNSC	TCGA-CX-7219	PDCD2L	SNP	Silent	19	34895682	G	T	40	45
KIRC	TCGA-CZ-5453	PDCD2L	SNP	Splice_Site	19	34904640	A	C	15	66
UCEC	TCGA-D1-A167	PDCD2L	SNP	Silent	19	34912478	C	T	23	45
BLCA	TCGA-DK-A1AB	PDCD2L	SNP	Missense_Mutation	19	34900411	C	A	21	61