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
IL1RAP	3556	genome.wustl.edu	37	3	190321985	190321985	+	Missense_Mutation	SNP	A	A	G			TCGA-HM-A6W2-01A-21D-A33O-09	TCGA-HM-A6W2-10A-01D-A33O-09	A	A					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	77da5f5d-4036-48c1-8992-651b8c0ed331	cd89b294-bf23-495d-a809-4ba324acc1ec	3	190321985	190321985	A	G	SNP	IL1RAP	ENST00000443369	human	ensembl	70_37	+1	known	missense	c.133	p.I45V	0.998	smart_Ig_sub,prints_IL1_rcpt_I/II	pfam_TIR_dom,superfamily_TIR_dom,smart_Ig_sub,smart_TIR_dom,pfscan_TIR_dom,pfscan_Ig-like,prints_IL1_rcpt_1,prints_IL1_rcpt_I/II	-	no_errors	IL1RAP	HGNC
OR4D5	219875	genome.wustl.edu	37	11	123811257	123811257	+	Missense_Mutation	SNP	C	C	G			TCGA-HM-A6W2-01A-21D-A33O-09	TCGA-HM-A6W2-10A-01D-A33O-09	C	C					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	77da5f5d-4036-48c1-8992-651b8c0ed331	cd89b294-bf23-495d-a809-4ba324acc1ec	11	123811257	123811257	C	G	SNP	OR4D5	ENST00000307033	human	ensembl	70_37	+1	known	missense	c.934	p.L312V	0.000	NULL	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_Olfact_rcpt,prints_GPCR_Rhodpsn	-	no_errors	OR4D5	HGNC
OR4D5	219875	genome.wustl.edu	37	11	123811269	123811269	+	Missense_Mutation	SNP	C	C	A			TCGA-HM-A6W2-01A-21D-A33O-09	TCGA-HM-A6W2-10A-01D-A33O-09	C	C					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	77da5f5d-4036-48c1-8992-651b8c0ed331	cd89b294-bf23-495d-a809-4ba324acc1ec	11	123811269	123811269	C	A	SNP	OR4D5	ENST00000307033	human	ensembl	70_37	+1	known	missense	c.946	p.P316T	0.001	NULL	pfam_GPCR_Rhodpsn,pfscan_GPCR_Rhodpsn_7TM,prints_Olfact_rcpt,prints_GPCR_Rhodpsn	-	no_errors	OR4D5	HGNC
PRDM2	7799	genome.wustl.edu	37	1	14107417	14107417	+	Missense_Mutation	SNP	G	G	T			TCGA-HM-A6W2-01A-21D-A33O-09	TCGA-HM-A6W2-10A-01D-A33O-09	G	G					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	77da5f5d-4036-48c1-8992-651b8c0ed331	cd89b294-bf23-495d-a809-4ba324acc1ec	1	14107417	14107417	G	T	SNP	PRDM2	ENST00000235372	human	ensembl	70_37	+1	known	missense	c.3127	p.A1043S	1.000	pirsf_RIZ_retinblastoma-bd_prot	pfam_SET_dom,smart_SET_dom,smart_Znf_C2H2-like,pirsf_RIZ_retinblastoma-bd_prot,pfscan_SET_dom,pfscan_Znf_C2H2	-	no_errors	PRDM2	HGNC