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	chromosome_name_WU	start_WU	stop_WU	reference_WU	variant_WU	type_WU	gene_name_WU	transcript_name_WU	transcript_species_WU	transcript_source_WU	transcript_version_WU	strand_WU	transcript_status_WU	trv_type_WU	c_position_WU	amino_acid_change_WU	ucsc_cons_WU	domain_WU	all_domains_WU	deletion_substructures_WU	transcript_error_WU
TCEAL3	85012	genome.wustl.edu	36	X	102751098	102751098	+	Silent	SNP	A	A	G			TCGA-AB-3000-03A-01D-0739-09	TCGA-AB-3000-11A-01D-0739-09	A	A			A	A	Unknown	Valid	Somatic		WGS	Illumina_Capture			Illumina GAIIx	X	102751098	102751098	A	G	SNP	TCEAL3	NM_001006933	human	genbank	54_36p	+1	reviewed	silent	c.450	p.Q150	1.000	HMMPfam_TFA	HMMPfam_TFA	-	no_errors
DYSF	8291	genome.wustl.edu	36	2	71648884	71648884	+	Silent	SNP	C	C	T			TCGA-AB-3000-03A-01D-0739-09	TCGA-AB-3000-11A-01D-0739-09	C	C			C	C	Unknown	Valid	Somatic		WGS	Illumina_Capture			Illumina GAIIx	2	71648884	71648884	C	T	SNP	DYSF	NM_003494	human	genbank	54_36p	+1	reviewed	silent	c.2718	p.D906	0.981	HMMSmart_SM00693	HMMPfam_C2,HMMSmart_SM00239,HMMSmart_SM00693,HMMSmart_SM00694,superfamily_C2 domain (Calcium/lipid-binding domain CaLB),HMMPfam_FerA,HMMPfam_FerB,HMMPfam_FerI	-	no_errors
CLCN6	1185	genome.wustl.edu	36	1	11820095	11820095	+	Missense_Mutation	SNP	G	G	C			TCGA-AB-3000-03A-01D-0739-09	TCGA-AB-3000-11A-01D-0739-09	G	G			G	G	Unknown	Valid	Somatic		WGS	Illumina_Capture			Illumina GAIIx	1	11820095	11820095	G	C	SNP	CLCN6	NM_001286	human	genbank	54_36p	+1	reviewed	missense	c.2247	p.Q749H	1.000	HMMPfam_CBS	HMMPfam_CBS,HMMSmart_SM00116,HMMPfam_Voltage_CLC,superfamily_Clc chloride channel,superfamily_CBS-domain	-	no_errors
LOC344875	344875	genome.wustl.edu	36	3	15181516	15181516	+	Missense_Mutation	SNP	C	C	A			TCGA-AB-3000-03A-01D-0739-09	TCGA-AB-3000-11A-01D-0739-09	C	C			C	C	Unknown	Valid	Somatic		WGS	Illumina_Capture			Illumina GAIIx	3	15181516	15181516	C	A	SNP	LOC344875	XM_497913	human	genbank	54_36p	-1	model	missense	c.2954	p.C985F	1.000	HMMSmart_SM00327,superfamily_vWA-like	HMMPfam_VWA,HMMSmart_SM00327,superfamily_vWA-like	-	no_errors
