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	chromosome_name	start	stop	reference	variant	type	gene_name	transcript_name	transcript_species	transcript_source	transcript_version	strand	transcript_status	trv_type	c_position	amino_acid_change	ucsc_cons	domain	all_domains	deletion_substructures	transcript_error	default_gene_name	gene_name_source
CROCCP2	84809	genome.wustl.edu	37	1	16956993	16956993	+	RNA	SNP	A	A	G			TCGA-C5-A2LY-01A-31D-A18J-09	TCGA-C5-A2LY-10A-01D-A18J-09	A	A					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	047f9e4d-86b5-4943-aef5-68199bf29e8c	433b41e8-d79a-4da0-a700-821cd97cc1b9	1	16956993	16956993	A	G	SNP	CROCCP2	ENST00000362058	human	ensembl	70_37	-1	known	rna	NULL	NULL	0.002	-	-	-	no_errors	CROCCP2	HGNC
FLNB	2317	genome.wustl.edu	37	3	58062875	58062875	+	Missense_Mutation	SNP	G	G	T			TCGA-C5-A2LY-01A-31D-A18J-09	TCGA-C5-A2LY-10A-01D-A18J-09	G	G					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	047f9e4d-86b5-4943-aef5-68199bf29e8c	433b41e8-d79a-4da0-a700-821cd97cc1b9	3	58062875	58062875	G	T	SNP	FLNB	ENST00000295956	human	ensembl	70_37	+1	known	missense	c.395	p.G132V	1.000	superfamily_CH-domain	pfam_Filamin/ABP280_repeat-like,pfam_CH-domain,superfamily_CH-domain,superfamily_Ig_E-set,smart_CH-domain,smart_Filamin,pfscan_CH-domain,pfscan_Filamin/ABP280_repeat-like	-	no_errors	FLNB	HGNC
LPAR1	1902	genome.wustl.edu	37	9	113704131	113704131	+	Nonsense_Mutation	SNP	C	C	T			TCGA-C5-A2LY-01A-31D-A18J-09	TCGA-C5-A2LY-10A-01D-A18J-09	C	C					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	047f9e4d-86b5-4943-aef5-68199bf29e8c	433b41e8-d79a-4da0-a700-821cd97cc1b9	9	113704131	113704131	C	T	SNP	LPAR1	ENST00000538760	human	ensembl	70_37	-1	known	nonsense	c.366	p.W122*	1.000	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_LPA_rcpt_EDG2	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_LPA_rcpt_EDG2,prints_LPA_rcpt,prints_GPCR_Rhodpsn	-	no_errors	LPAR1	HGNC
OR2S2	56656	genome.wustl.edu	37	9	35957557	35957557	+	Missense_Mutation	SNP	C	C	A			TCGA-C5-A2LY-01A-31D-A18J-09	TCGA-C5-A2LY-10A-01D-A18J-09	C	C					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	047f9e4d-86b5-4943-aef5-68199bf29e8c	433b41e8-d79a-4da0-a700-821cd97cc1b9	9	35957557	35957557	C	A	SNP	OR2S2	ENST00000341959	human	ensembl	70_37	-1	known	missense	c.539	p.C180F	1.000	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_Olfact_rcpt	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_Olfact_rcpt,prints_GPCR_Rhodpsn	-	no_errors	OR2S2	HGNC