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	NormalRefReads_WU	NormalVarReads_WU	NormalVAF_WU	TumorRefReads_WU	TumorVarReads_WU	TumorVAF_WU	RNARefReads_WU	RNAVarReads_WU	RNAVAF_WU
FAM194A	0	genome.wustl.edu	36	3	151867361	151867361	+	Missense_Mutation	SNP	C	C	T			TCGA-AB-2957-03A-01W-0733-08	TCGA-AB-2957-11A-01W-0732-08	C	C	C	T	C	C	Verified	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq	1	dbGAP	Illumina HiSeq	916a9b37-ed97-4a68-b9ce-4d9e2c419ccd	945dd1e2-500a-420f-8f6b-d46ce2ec67d3	3	151867361	151867361	C	T	SNP	C3orf44	NM_152394.3	human	genbank	54_36p	-1	validated	missense	c.1631	p.R544H	0.548	NULL	NULL	-	no_errors	51	3	5.36	64	46	41.82	NA	NA	NA
uc001msu.1	0	genome.wustl.edu	36	11	31043202	31043202	+	Silent	SNP	G	G	A			TCGA-AB-2957-03A-01W-0733-08	TCGA-AB-2957-11A-01W-0732-08	G	G	G	A	G	G	Verified	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq	1	dbGAP	Illumina HiSeq	916a9b37-ed97-4a68-b9ce-4d9e2c419ccd	945dd1e2-500a-420f-8f6b-d46ce2ec67d3	11	31043202	31043202	G	A	SNP	uc001msu.1	ENST00000342355	human	ensembl	54_36p	-1	known	silent	c.1230	p.H410	0.454	superfamily_RicinB_like	superfamily_RicinB_like	-	no_errors	44	2	4.26	28	23	45.10	NA	NA	NA
FLT3	0	genome.wustl.edu	36	13	27490642	27490642	+	Missense_Mutation	SNP	C	C	A	rs121913488		TCGA-AB-2957-03A-01W-0733-08	TCGA-AB-2957-11A-01W-0732-08	C	C	C	A	C	C	Verified	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq	1	dbGAP	Illumina HiSeq	916a9b37-ed97-4a68-b9ce-4d9e2c419ccd	945dd1e2-500a-420f-8f6b-d46ce2ec67d3	13	27490642	27490642	C	A	SNP	FLT3	NM_004119.2	human	genbank	54_36p	-1	reviewed	missense	c.2503	p.D835Y	1.000	HMMPfam_Pkinase_Tyr,HMMSmart_TyrKc,superfamily_Kinase_like	HMMPfam_Pkinase_Tyr,HMMSmart_TyrKc,PatternScan_RECEPTOR_TYR_KIN_III,PatternScan_PROTEIN_KINASE_TYR,superfamily_Kinase_like,HMMPfam_ig,PatternScan_PROTEIN_KINASE_ATP,superfamily_SSF48726	-	no_errors	75	14	15.73	29	24	45.28	NA	NA	NA