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
OR10K1	391109	hgsc.bcm.edu	hg19	1	158435869	158435869	+	Missense_Mutation	SNP	A	A	G	novel		TCGA-BC-A10X-01A-11D-A12Z-10	TCGA-BC-A10X-11A-11D-A12Z-10	A	A	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	36938443-c826-4abe-aaf6-dd7217b07f51	4285989b-f8d8-4ced-99a1-894ff2b37cf3	.	OR10K1	NM_001004473	exon1	c.A518G	p.Q173R	CCAACCAGCTCCA	.	447.0	18.0	538.0	0.0	.	80	.	.	Atlas-SNP
OR2C3	81472	hgsc.bcm.edu	hg19	1	247694952	247694952	+	Missense_Mutation	SNP	G	G	T	rs201468915	by1000genomes;alternate_allele	TCGA-BC-A10X-01A-11D-A12Z-10	TCGA-BC-A10X-11A-11D-A12Z-10	G	G	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	36938443-c826-4abe-aaf6-dd7217b07f51	4285989b-f8d8-4ced-99a1-894ff2b37cf3	.	OR2C3	NM_198074	exon2	c.C862A	p.P288T	TAAGTGGGTTCAG	.	147.0	7.0	145.0	0.0	.	92	.	G|1.000;A|0.000	Atlas-SNP
COX3	5742	hgsc.bcm.edu	hg19	MT	9939	9939	+	Missense_Mutation	SNP	G	G	A	novel		TCGA-BC-A10X-01A-11D-A12Z-10	TCGA-BC-A10X-11A-11D-A12Z-10	G	G	.	.	.	.	Unknown	Untested	Somatic	PhaseI	WXS	none	.	.	Illumina HiSeq	36938443-c826-4abe-aaf6-dd7217b07f51	4285989b-f8d8-4ced-99a1-894ff2b37cf3	.	.	ENST00000362079	exon1	c.G733A	p.V245M	CATTTTGTAGATG	.	364.0	30.0	391.0	0.0	.	.	.	.	Atlas-SNP