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	HGVS_genomic_change	HGVS_coding_DNA_change	HGVS_protein_change	HGVSp_Short	transcript_change	transcript_exon	HGNC_RefSeq	Tumor_Sample_Barcode	totalDepth	refDepth	altDepth	VariantFreq	Feature	HGVSc	HGVSp	Protein_position	Clinvar	SampleID	ExonicFunc.refGene	cytoBand	CLNSIG	avsnp150	cosmic87	X1000g2015aug_all	ExAC_ALL	ExAC_AFR	ExAC_AMR	ExAC_EAS	ExAC_FIN	ExAC_NFE	ExAC_OTH	ExAC_SAS	gnomAD_exome_ALL	gnomAD_exome_AFR	gnomAD_exome_AMR	gnomAD_exome_ASJ	gnomAD_exome_EAS	gnomAD_exome_FIN	gnomAD_exome_NFE	gnomAD_exome_OTH	gnomAD_exome_SAS	Kaviar_AF	Kaviar_AC	Kaviar_AN	SIFT_pred	LRT_pred	MutationTaster_pred	MutationAssessor_pred	FATHMM_pred	PROVEAN_pred	MetaSVM_pred	MetaLR_pred	M.CAP_pred	fathmm.MKL_coding_pred	BRCA_Clinvar	BRCA_Enigma	cancer_type	oncogenic	oncokb_level	oncokb_resistance_level	oncokb_drugs	oncokb_version	cosmicCount
AR	367	.	hg19	chrX	66931463	66931463	+	Missense_Mutation	SNP	T	T	A	X:g.66931463T>A	ENST00000374690.3:c.2105T>A	ENSP00000363822:p.Leu702His	p.L702H	c.2105T>A	4	NM_000044	P000388_C	6622	6594	28	0.422832981	ENST00000374690	c.2105T>A	p.Leu702His	702	likely_pathogenic:1	P000388	nonsynonymous SNV	Xq12	Likely_pathogenic	rs864622007	"ID=COSM5559925,COSM238553,COSM238554;OCCURENCE=1(large_intestine),51(prostate)"	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	D	D	D	M	D	D	D	D	D	D	NA	NA	CANCER	NA	NA	NA	NA	v1.19_patch_1	52
AR	367	.	hg19	chrX	66931463	66931463	+	Missense_Mutation	SNP	T	T	A	X:g.66931463T>A	ENST00000374690.3:c.2105T>A	ENSP00000363822:p.Leu702His	p.L702H	c.2105T>A	4	NM_000044	P000568_C	7649	7630	19	0.248398483	ENST00000374690	c.2105T>A	p.Leu702His	702	likely_pathogenic:1	P000568	nonsynonymous SNV	Xq12	Likely_pathogenic	rs864622007	"ID=COSM5559925,COSM238553,COSM238554;OCCURENCE=1(large_intestine),51(prostate)"	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	D	D	D	M	D	D	D	D	D	D	NA	NA	CANCER	NA	NA	NA	NA	v1.19_patch_1	52
SMO	6608	.	hg19	chr7	128852033	128852033	+	Missense_Mutation	SNP	C	C	G	7:g.128852033C>G	ENST00000249373.3:c.2105C>G	ENSP00000249373:p.Pro702Arg	p.P702R	c.2105C>G	12	NM_005631	P001174BSD	6004	5986	18	0.299800133	ENST00000249373	c.2105C>G	p.Pro702Arg	702	NA	P001174BSD	nonsynonymous SNV	7q32.1	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	.	D	D	D	L	D	N	D	D	D	D	NA	NA	CANCER	NA	NA	NA	NA	v1.19_patch_1	0