ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
DLBCL	DLBCL-Ls420	CAB39L	SNP	Missense_Mutation	13	49956945	C	A	32	63
LUAD	LUAD-F00257	CAB39L	SNP	Missense_Mutation	13	49951261	C	G	32	99
LUAD	LUAD-RT-S01700	CAB39L	SNP	Missense_Mutation	13	49885057	C	G	29	97
MEL	MEL-JWCI-14	CAB39L	SNP	Missense_Mutation	13	49956962	C	T	30	97
MEL	MEL-Ma-Mel-105	CAB39L	SNP	Missense_Mutation	13	49913872	C	T	29	73
LUAD	TCGA-05-4396	CAB39L	SNP	Missense_Mutation	13	49906129	C	A	23	100
LUAD	TCGA-05-4410	CAB39L	SNP	Missense_Mutation	13	49951249	T	C	61	90
LUSC	TCGA-37-3789	CAB39L	SNP	Missense_Mutation	13	49885033	C	G	32	96
UCEC	TCGA-A5-A0GP	CAB39L	SNP	Missense_Mutation	13	49924940	G	T	33	60
BRCA	TCGA-A8-A09I	CAB39L	SNP	Silent	13	49925033	C	T	32	70
CRC	TCGA-AA-3977	CAB39L	SNP	Silent	13	49951199	T	C	60	52
CRC	TCGA-AA-A010	CAB39L	SNP	Missense_Mutation	13	49913861	C	A	32	65
CRC	TCGA-AG-3892	CAB39L	SNP	Silent	13	49933954	C	T	29	57
CRC	TCGA-AG-A002	CAB39L	SNP	Nonsense_Mutation	13	49957001	C	A	32	97
UCEC	TCGA-AX-A05T	CAB39L	SNP	Missense_Mutation	13	49884970	A	C	3	69
UCEC	TCGA-AX-A0J0	CAB39L	SNP	Missense_Mutation	13	49933943	A	C	1	90
UCEC	TCGA-B5-A0JY	CAB39L	SNP	Missense_Mutation	13	49924940	G	T	33	60
UCEC	TCGA-BG-A0M3	CAB39L	SNP	Missense_Mutation	13	49925022	C	T	19	72
UCEC	TCGA-BS-A0UF	CAB39L	SNP	Missense_Mutation	13	49924992	C	T	31	100
UCEC	TCGA-BS-A0UJ	CAB39L	SNP	Splice_Site	13	49885131	T	C	55	89
UCEC	TCGA-BS-A0UV	CAB39L	SNP	Missense_Mutation	13	49924992	C	T	31	100
UCEC	TCGA-BS-A0UV	CAB39L	SNP	Silent	13	49933933	G	T	33	56
HNSC	TCGA-CR-7398	CAB39L	SNP	Nonsense_Mutation	13	49957001	C	A	32	97
HNSC	TCGA-DQ-7595	CAB39L	SNP	Missense_Mutation	13	49925023	G	T	40	82