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	Transcript_Id	Exon	ChromChange	AAChange	Genome_Plus_Minus_10_Bp	Drug_Target	TTotCov	TVarCov	NTotCov	NVarCov	dbSNPPopFreq	COSMIC_Gene_Freq	COSMIC_Site_Freq	dbSNP_AF	Algorithm
PCDHGB4	8641	hgsc.bcm.edu	hg19	5	140769325	140769325	+	Missense_Mutation	SNP	G	G	A	rs201153580	bycluster;alternate_allele	TCGA-ED-A627-01A-12D-A30V-10	TCGA-ED-A627-10B-01D-A30V-10	G	G	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	f59d69bf-3766-4425-a07e-7b5a15b05580	52ca40d4-025d-419f-acf2-feeca914604d	.	PCDHGB4	NM_032098	exon1	c.G1874A	p.R625H	AAGTGCGCACAGC	.	55.0	4.0	43.0	0.0	.	125	.	.	Atlas-SNP
SUPT16H	11198	hgsc.bcm.edu	hg19	14	21820872	21820872	+	Missense_Mutation	SNP	G	G	T	novel		TCGA-ED-A627-01A-12D-A30V-10	TCGA-ED-A627-10B-01D-A30V-10	G	G	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	f59d69bf-3766-4425-a07e-7b5a15b05580	52ca40d4-025d-419f-acf2-feeca914604d	.	SUPT16H	NM_007192	exon26	c.C3104A	p.S1035Y	TGTCTGGAACCAC	.	72.0	5.0	56.0	0.0	.	84	.	.	Atlas-SNP
HLX	3142	hgsc.bcm.edu	hg19	1	221053601	221053602	+	In_Frame_Ins	INS	-	-	CAGCAACAGCCGCCG	novel		TCGA-ED-A627-01A-12D-A30V-10	TCGA-ED-A627-10B-01D-A30V-10	-	-	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	f59d69bf-3766-4425-a07e-7b5a15b05580	52ca40d4-025d-419f-acf2-feeca914604d	.	HLX	NM_021958	exon1	c.402_403insCAGCAACAGCCGCCG	p.Q134delinsQQQQPP	.	.	86.0	14.0	85.0	0.0	.	67	.	.	Atlas-INDEL
