Hugo_Symbol	Entrez_Gene_Id	Center	NCBI_Build	Chromosome	Start_position	End_position	Strand	Variant_Classification	Variant_Type	Reference_Allele	Tumor_Seq_Allele1	Tumor_Seq_Allele2	dbSNP_RS	dbSNP_Val_Status	Tumor_Sample_Barcode	Matched_Norm_Sample_Barcode	Match_Norm_Seq_Allele1	Match_Norm_Seq_Allele2	Tumor_Validation_Allele1	Tumor_Validation_Allele2	Match_Norm_Validation_Allele1	Match_Norm_Validation_Allele2	Verification_Status	Validation_Status	Mutation_Status	Sequencing_Phase	Sequence_Source	Validation_Method	Score	BAM_File	Sequencer	Tumor_Sample_UUID	Matched_Norm_Sample_UUID	COSMIC_Codon	COSMIC_Gene	TranscriptID	Exon	ChromChange	AAChange	Genome_Plus_Minus_10_Bp	Drug_Target	TTotCov	TVarCov	NTotCov	NVarCov	dbSNPPopFreq	COSMIC_Gene_Freq
PARP4	143	ucsc.edu;bcgsc.ca	37	13	25058867	25058867	+	Missense_Mutation	SNP	C	C	T	rs201518768		TCGA-ED-A627-01A-12D-A30V-10	TCGA-ED-A627-10B-01D-A30V-10	C	C	.	.	.	.	Unknown	Untested	Somatic	.	WXS	none	.	.	Illumina HiSeq	f59d69bf-3766-4425-a07e-7b5a15b05580	52ca40d4-025d-419f-acf2-feeca914604d	.	PARP4	NM_006437	exon12	c.G1372A	p.V458I	CCACTACTTTGGG	.	119.0	17.0	95.0	1.0	.	94
TBX2	6909	broad.mit.edu;ucsc.edu	37	17	59479224	59479224	+	Missense_Mutation	SNP	G	G	T	novel		TCGA-ED-A627-01A-12D-A30V-10	TCGA-ED-A627-10B-01D-A30V-10	G	G	.	.	.	.	.	Untested	Somatic	Phase_I	WXS	none	.	.	Illumina HiSeq	f59d69bf-3766-4425-a07e-7b5a15b05580	52ca40d4-025d-419f-acf2-feeca914604d	.	TBX2	NM_005994	exon2	c.G575T	p.S192I	CAGACAGCCCAGC	.	38.0	7.0	49.0	0.0	.	226