#version 2.4
## 
## Oncotator v1.8.0.0 | Flat File Reference hg19 | GENCODE v19 EFFECT | UniProt_AAxform 2014_12 | ClinVar 12.03.20 | ESP 6500SI-V2 | ORegAnno UCSC Track | dbSNP build 142 | CCLE_By_GP 09292010 | COSMIC v62_291112 | 1000gp3 20130502 | UniProt_AA 2014_12 | dbNSFP v2.4 | ESP 6500SI-V2 | COSMIC_FusionGenes v62_291112 | gencode_xref_refseq metadata_v19 | CCLE_By_Gene 09292010 | ACHILLES_Lineage_Results 110303 | CGC full_2012-03-15 | UniProt 2014_12 | HumanDNARepairGenes 20110905 | HGNC Sept172014 | COSMIC_Tissue 291112 | Familial_Cancer_Genes 20110905 | TUMORScape 20100104 | Ensembl ICGC MUCOPA | TCGAScape 110405 | MutSig Published Results 20110905 
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	Genome_Change	Annotation_Transcript	Transcript_Strand	Transcript_Exon	Transcript_Position	cDNA_Change	Codon_Change	Protein_Change	Other_Transcripts	Refseq_mRNA_Id	Refseq_prot_Id	SwissProt_acc_Id	SwissProt_entry_Id	Description	UniProt_AApos	UniProt_Region	UniProt_Site	UniProt_Natural_Variations	UniProt_Experimental_Info	GO_Biological_Process	GO_Cellular_Component	GO_Molecular_Function	COSMIC_overlapping_mutations	COSMIC_fusion_genes	COSMIC_tissue_types_affected	COSMIC_total_alterations_in_gene	Tumorscape_Amplification_Peaks	Tumorscape_Deletion_Peaks	TCGAscape_Amplification_Peaks	TCGAscape_Deletion_Peaks	DrugBank	ref_context	gc_content	CCLE_ONCOMAP_overlapping_mutations	CCLE_ONCOMAP_total_mutations_in_gene	CGC_Mutation_Type	CGC_Translocation_Partner	CGC_Tumor_Types_Somatic	CGC_Tumor_Types_Germline	CGC_Other_Diseases	DNARepairGenes_Role	FamilialCancerDatabase_Syndromes	MUTSIG_Published_Results	OREGANNO_ID	OREGANNO_Values	i_1000gp3_AA	i_1000gp3_AC	i_1000gp3_AF	i_1000gp3_AFR_AF	i_1000gp3_AMR_AF	i_1000gp3_AN	i_1000gp3_CIEND	i_1000gp3_CIPOS	i_1000gp3_CS	i_1000gp3_DP	i_1000gp3_EAS_AF	i_1000gp3_END	i_1000gp3_EUR_AF	i_1000gp3_IMPRECISE	i_1000gp3_MC	i_1000gp3_MEINFO	i_1000gp3_MEND	i_1000gp3_MLEN	i_1000gp3_MSTART	i_1000gp3_NS	i_1000gp3_SAS_AF	i_1000gp3_SVLEN	i_1000gp3_SVTYPE	i_1000gp3_TSD	i_ACHILLES_Lineage_Results_Top_Genes	i_BAM_File	i_CAF	i_CGC_Cancer Germline Mut	i_CGC_Cancer Molecular Genetics	i_CGC_Cancer Somatic Mut	i_CGC_Cancer Syndrome	i_CGC_Chr	i_CGC_Chr Band	i_CGC_GeneID	i_CGC_Name	i_CGC_Other Germline Mut	i_CGC_Tissue Type	i_COSMIC_n_overlapping_mutations	i_COSMIC_overlapping_mutation_descriptions	i_COSMIC_overlapping_primary_sites	i_ClinVar_ASSEMBLY	i_ClinVar_HGMD_ID	i_ClinVar_SYM	i_ClinVar_TYPE	i_ClinVar_rs	i_ESP_AA	i_ESP_AAC	i_ESP_AA_AC	i_ESP_AA_AGE	i_ESP_AA_GTC	i_ESP_AvgAAsampleReadDepth	i_ESP_AvgEAsampleReadDepth	i_ESP_AvgSampleReadDepth	i_ESP_CA	i_ESP_CDP	i_ESP_CG	i_ESP_CP	i_ESP_Chromosome	i_ESP_DBSNP	i_ESP_DP	i_ESP_EA_AC	i_ESP_EA_AGE	i_ESP_EA_GTC	i_ESP_EXOME_CHIP	i_ESP_FG	i_ESP_GL	i_ESP_GM	i_ESP_GS	i_ESP_GTC	i_ESP_GTS	i_ESP_GWAS_PUBMED	i_ESP_MAF	i_ESP_PH	i_ESP_PP	i_ESP_Position	i_ESP_TAC	i_ESP_TotalAAsamplesCovered	i_ESP_TotalEAsamplesCovered	i_ESP_TotalSamplesCovered	i_Ensembl_so_accession	i_Ensembl_so_term	i_Entrez_Gene_Id	i_Familial_Cancer_Genes_Reference	i_Familial_Cancer_Genes_Synonym	i_HGNC_Accession Numbers	i_HGNC_CCDS IDs	i_HGNC_Chromosome	i_HGNC_Date Modified	i_HGNC_Date Name Changed	i_HGNC_Date Symbol Changed	i_HGNC_Ensembl Gene ID	i_HGNC_Ensembl ID(supplied by Ensembl)	i_HGNC_Enzyme IDs	i_HGNC_Gene family description	i_HGNC_HGNC ID	i_HGNC_Locus Group	i_HGNC_Locus Type	i_HGNC_Name Synonyms	i_HGNC_OMIM ID(supplied by NCBI)	i_HGNC_Previous Names	i_HGNC_Previous Symbols	i_HGNC_Primary IDs	i_HGNC_Pubmed IDs	i_HGNC_Record Type	i_HGNC_RefSeq(supplied by NCBI)	i_HGNC_Secondary IDs	i_HGNC_Status	i_HGNC_Synonyms	i_HGNC_UCSC ID(supplied by UCSC)	i_HGNC_UniProt ID(supplied by UniProt)	i_HGNC_VEGA IDs	i_HGVS_coding_DNA_change	i_HGVS_genomic_change	i_HGVS_protein_change	i_ORegAnno_bin	i_UniProt_alt_uniprot_accessions	i_Variant_Classification	i_Variant_Type	i_all_domains	i_amino_acid_change	i_annotation_transcript	i_build	i_c_position	i_ccds_id	i_chromosome_name	i_dbNSFP_1000Gp1_AC	i_dbNSFP_1000Gp1_AF	i_dbNSFP_1000Gp1_AFR_AC	i_dbNSFP_1000Gp1_AFR_AF	i_dbNSFP_1000Gp1_AMR_AC	i_dbNSFP_1000Gp1_AMR_AF	i_dbNSFP_1000Gp1_ASN_AC	i_dbNSFP_1000Gp1_ASN_AF	i_dbNSFP_1000Gp1_EUR_AC	i_dbNSFP_1000Gp1_EUR_AF	i_dbNSFP_Ancestral_allele	i_dbNSFP_CADD_phred	i_dbNSFP_CADD_raw	i_dbNSFP_CADD_raw_rankscore	i_dbNSFP_ESP6500_AA_AF	i_dbNSFP_ESP6500_EA_AF	i_dbNSFP_Ensembl_geneid	i_dbNSFP_Ensembl_transcriptid	i_dbNSFP_FATHMM_pred	i_dbNSFP_FATHMM_rankscore	i_dbNSFP_FATHMM_score	i_dbNSFP_GERP++_NR	i_dbNSFP_GERP++_RS	i_dbNSFP_GERP++_RS_rankscore	i_dbNSFP_Interpro_domain	i_dbNSFP_LRT_Omega	i_dbNSFP_LRT_converted_rankscore	i_dbNSFP_LRT_pred	i_dbNSFP_LRT_score	i_dbNSFP_LR_pred	i_dbNSFP_LR_rankscore	i_dbNSFP_LR_score	i_dbNSFP_MutationAssessor_pred	i_dbNSFP_MutationAssessor_rankscore	i_dbNSFP_MutationAssessor_score	i_dbNSFP_MutationTaster_converted_rankscore	i_dbNSFP_MutationTaster_pred	i_dbNSFP_MutationTaster_score	i_dbNSFP_Polyphen2_HDIV_pred	i_dbNSFP_Polyphen2_HDIV_rankscore	i_dbNSFP_Polyphen2_HDIV_score	i_dbNSFP_Polyphen2_HVAR_pred	i_dbNSFP_Polyphen2_HVAR_rankscore	i_dbNSFP_Polyphen2_HVAR_score	i_dbNSFP_RadialSVM_pred	i_dbNSFP_RadialSVM_rankscore	i_dbNSFP_RadialSVM_score	i_dbNSFP_Reliability_index	i_dbNSFP_SIFT_converted_rankscore	i_dbNSFP_SIFT_pred	i_dbNSFP_SIFT_score	i_dbNSFP_SLR_test_statistic	i_dbNSFP_SiPhy_29way_logOdds	i_dbNSFP_SiPhy_29way_logOdds_rankscore	i_dbNSFP_SiPhy_29way_pi	i_dbNSFP_UniSNP_ids	i_dbNSFP_Uniprot_aapos	i_dbNSFP_Uniprot_acc	i_dbNSFP_Uniprot_id	i_dbNSFP_aaalt	i_dbNSFP_aapos	i_dbNSFP_aapos_FATHMM	i_dbNSFP_aapos_SIFT	i_dbNSFP_aaref	i_dbNSFP_cds_strand	i_dbNSFP_codonpos	i_dbNSFP_fold-degenerate	i_dbNSFP_genename	i_dbNSFP_hg18_pos(1-coor)	i_dbNSFP_phastCons100way_vertebrate	i_dbNSFP_phastCons100way_vertebrate_rankscore	i_dbNSFP_phastCons46way_placental	i_dbNSFP_phastCons46way_placental_rankscore	i_dbNSFP_phastCons46way_primate	i_dbNSFP_phastCons46way_primate_rankscore	i_dbNSFP_phyloP100way_vertebrate	i_dbNSFP_phyloP100way_vertebrate_rankscore	i_dbNSFP_phyloP46way_placental	i_dbNSFP_phyloP46way_placental_rankscore	i_dbNSFP_phyloP46way_primate	i_dbNSFP_phyloP46way_primate_rankscore	i_dbNSFP_refcodon	i_deletion_substructures	i_domain	i_entrez_gene_id	i_gc_content_full	i_gencode_transcript_name	i_gencode_transcript_status	i_gencode_transcript_tags	i_gencode_transcript_type	i_gene_name	i_gene_type	i_havana_transcript	i_normal_ref_reads	i_normal_ref_reads_val	i_normal_vaf	i_normal_vaf_val	i_normal_var_reads	i_normal_var_reads_val	i_reference	i_refseq_mrna_id	i_rsID	i_rsID_ref_var_alleles	i_secondary_variant_classification	i_stop	i_strand	i_transcript_error	i_transcript_name	i_transcript_source	i_transcript_species	i_transcript_status	i_transcript_version	i_trv_type	i_tumor_ref_reads	i_tumor_ref_reads_val	i_tumor_vaf	i_tumor_vaf_val	i_tumor_var_reads	i_tumor_var_reads_val	i_type	i_ucsc_cons	i_variant
SMAP2	64744	genome.wustl.edu	37	1	40872437	40872437	+	5'UTR	SNP	G	G	T			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	G	G	G	T	G	G	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr1:40872437G>T	ENST00000539317.1	+	0	86					NM_001198980.1	NP_001185909.1	Q8WU79	SMAP2_HUMAN	small ArfGAP2						regulation of ARF GTPase activity (GO:0032312)	cytoplasm (GO:0005737)|nucleus (GO:0005634)	ARF GTPase activator activity (GO:0008060)|zinc ion binding (GO:0008270)			central_nervous_system(3)|kidney(1)|large_intestine(7)|lung(9)|ovary(1)|pancreas(2)|upper_aerodigestive_tract(1)	24	Lung NSC(20;1.56e-05)|Ovarian(52;0.00769)|all_hematologic(146;0.0501)|Acute lymphoblastic leukemia(166;0.074)	Myeloproliferative disorder(586;0.0393)	OV - Ovarian serous cystadenocarcinoma(33;1.04e-17)			GAACATTGGTGTGTTCATCTG	0.453																																							0											0													102.0	99.0	100.0					1																	40872437		2203	4300	6503	SO:0001623	5_prime_UTR_variant	0			AL137764	CCDS451.1, CCDS55592.1, CCDS55593.1, CCDS72763.1	1p35.3-p34.1	2008-09-22	2008-09-05	2008-01-09	ENSG00000084070	ENSG00000084070		"""ADP-ribosylation factor GTPase activating proteins"""	25082	protein-coding gene	gene with protein product			"""stromal membrane-associated protein 1-like"", ""stromal membrane-associated GTPase-activating protein 2"""	SMAP1L		16571680	Standard	NM_001198978		Approved		uc001cfj.3	Q8WU79	OTTHUMG00000007301	ENST00000539317.1:c.-108G>T	1.37:g.40872437G>T			B2R7T1|B7Z5B5|B7Z8V2|D3DPV2|Q5QPL2|Q96C93|Q9NST2|Q9UJL8	Missense_Mutation	SNP	pfam_ArfGAP,smart_ArfGAP,pfscan_ArfGAP,prints_ArfGAP	p.V45L	ENST00000539317.1	37	c.133	CCDS55593.1	1	.	.	.	.	.	.	.	.	.	.	G	20.8	4.046180	0.75846	.	.	ENSG00000084070	ENST00000435168;ENST00000372718;ENST00000372708	T;T	0.51817	0.69;0.69	6.06	6.06	0.98353	.	0.049956	0.85682	D	0.000000	T	0.58192	0.2105	M	0.79926	2.475	0.80722	D	1	P;P	0.46706	0.851;0.883	B;B	0.44224	0.444;0.43	T	0.63897	-0.6533	10	0.62326	D	0.03	-3.9597	18.1147	0.89549	0.0:0.0:1.0:0.0	.	15;45	Q8WU79-2;Q8WU79	.;SMAP2_HUMAN	L	45;45;15	ENSP00000361803:V45L;ENSP00000361793:V15L	ENSP00000361793:V15L	V	+	1	0	SMAP2	40645024	1.000000	0.71417	1.000000	0.80357	0.999000	0.98932	4.518000	0.60510	2.882000	0.98803	0.655000	0.94253	GTG	0	pfam_ArfGAP,smart_ArfGAP,pfscan_ArfGAP,prints_ArfGAP		0.453	SMAP2-201	KNOWN	basic|CCDS	protein_coding	SMAP2	protein_coding		59	201	0	0.00	0	0	G	NM_022733	0	0		40872437	1	no_errors	ENST00000372718	ensembl	human	known	74_37	missense	39	146	13.04	8.07	6	13	SNP	0.998	T
OCIAD2	132299	genome.wustl.edu	37	4	48906563	48906563	+	Missense_Mutation	SNP	C	C	G			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	C	C	C	G	C	C	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr4:48906563C>G	ENST00000508632.1	-	2	236	c.4G>C	c.(4-6)Gct>Cct	p.A2P	OCIAD2_ENST00000508069.2_5'UTR|OCIAD2_ENST00000273860.4_Missense_Mutation_p.A2P	NM_001014446.1	NP_001014446.1	Q56VL3	OCAD2_HUMAN	OCIA domain containing 2	2	OCIA.					endosome (GO:0005768)|mitochondrial inner membrane (GO:0005743)				kidney(1)|lung(3)|skin(1)|urinary_tract(1)	6						GACGCTGAAGCCATGATGACT	0.428																																							0											0													196.0	165.0	175.0					4																	48906563		2203	4300	6503	SO:0001583	missense	0			BC032808	CCDS3485.1, CCDS33981.1	4p12	2013-10-11			ENSG00000145247	ENSG00000145247			28685	protein-coding gene	gene with protein product						17054434	Standard	NM_001286774		Approved	MGC45416	uc003gyt.3	Q56VL3	OTTHUMG00000128626	ENST00000508632.1:c.4G>C	4.37:g.48906563C>G	ENSP00000423014:p.Ala2Pro		B4DPE7|Q8N544	Missense_Mutation	SNP	pfam_OCIA	p.A2P	ENST00000508632.1	37	c.4	CCDS33981.1	4	.	.	.	.	.	.	.	.	.	.	C	11.72	1.723193	0.30503	.	.	ENSG00000145247	ENST00000508632;ENST00000273860;ENST00000381464	T;T;T	0.54675	0.6;0.56;0.57	4.19	2.46	0.29980	.	0.392254	0.22859	N	0.054778	T	0.43322	0.1242	L	0.36672	1.1	0.27441	N	0.953706	P;P	0.45176	0.852;0.769	P;B	0.46253	0.509;0.216	T	0.24012	-1.0172	9	.	.	.	-5.1375	6.7239	0.23345	0.0:0.7822:0.0:0.2178	.	2;2	Q56VL3-2;Q56VL3	.;OCAD2_HUMAN	P	2	ENSP00000423014:A2P;ENSP00000273860:A2P;ENSP00000370873:A2P	.	A	-	1	0	OCIAD2	48601320	1.000000	0.71417	0.844000	0.33320	0.002000	0.02628	1.172000	0.31908	0.525000	0.28522	-0.150000	0.13652	GCT	0	NULL		0.428	OCIAD2-002	KNOWN	basic|appris_principal|CCDS	protein_coding	OCIAD2	protein_coding	OTTHUMT00000361984.5	82	249	0	0.00	0	0	C	NM_152398	0	0		48906563	-1	no_errors	ENST00000508632	ensembl	human	known	74_37	missense	46	181	11.54	11.27	6	23	SNP	0.975	G
RAI14	26064	genome.wustl.edu	37	5	34811968	34811968	+	Silent	SNP	A	A	G			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	A	A	A	G	A	A	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr5:34811968A>G	ENST00000265109.3	+	9	941	c.654A>G	c.(652-654)ggA>ggG	p.G218G	RAI14_ENST00000428746.2_Silent_p.G218G|RAI14_ENST00000515799.1_Silent_p.G221G|RAI14_ENST00000503673.1_Silent_p.G218G|RAI14_ENST00000506376.1_Silent_p.G210G|RAI14_ENST00000397449.1_Silent_p.G211G|RAI14_ENST00000512629.1_Silent_p.G218G	NM_001145522.1|NM_015577.2	NP_001138994.1|NP_056392.2	Q9P0K7	RAI14_HUMAN	retinoic acid induced 14	218						actin cytoskeleton (GO:0015629)|cytoplasm (GO:0005737)|mitochondrion (GO:0005739)|nucleus (GO:0005634)				breast(2)|central_nervous_system(1)|endometrium(2)|kidney(4)|large_intestine(19)|lung(22)|ovary(1)|prostate(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	56	all_lung(31;0.000191)					ATTCTCTTGGATACAATGCCT	0.393																																							0											0													86.0	89.0	88.0					5																	34811968		2203	4300	6503	SO:0001819	synonymous_variant	0			AB037755	CCDS34142.1, CCDS54837.1, CCDS54838.1, CCDS54839.1	5p13.3-p13.2	2013-01-10			ENSG00000039560	ENSG00000039560		"""Ankyrin repeat domain containing"""	14873	protein-coding gene	gene with protein product	"""novel retinal pigment epithelial"""	606586				11042181	Standard	NM_015577		Approved	NORPEG, KIAA1334, RAI13, DKFZp564G013	uc011coj.2	Q9P0K7	OTTHUMG00000162019	ENST00000265109.3:c.654A>G	5.37:g.34811968A>G			E9PED3|Q6V1W9|Q7Z5I4|Q7Z733|Q9P2L2|Q9Y3T5	Silent	SNP	pfam_Ankyrin_rpt,superfamily_Ankyrin_rpt-contain_dom,superfamily_t-SNARE,superfamily_UBA-like,smart_Ankyrin_rpt,pfscan_Ankyrin_rpt,pfscan_Ankyrin_rpt-contain_dom,prints_Ankyrin_rpt	p.G221	ENST00000265109.3	37	c.663	CCDS34142.1	5																																																																																			0	superfamily_Ankyrin_rpt-contain_dom,smart_Ankyrin_rpt,pfscan_Ankyrin_rpt-contain_dom		0.393	RAI14-002	KNOWN	alternative_5_UTR|basic|appris_principal|CCDS	protein_coding	RAI14	protein_coding	OTTHUMT00000366786.1	73	306	0	0.00	0	0	A	NM_015577	0	0		34811968	1	no_errors	ENST00000515799	ensembl	human	known	74_37	silent	56	292	9.68	5.50	6	17	SNP	1	G
MAP3K1	4214	genome.wustl.edu	37	5	56179432	56179432	+	Missense_Mutation	SNP	A	A	G			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	A	A	A	G	A	A	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr5:56179432A>G	ENST00000399503.3	+	15	3745	c.3745A>G	c.(3745-3747)Ata>Gta	p.I1249V		NM_005921.1	NP_005912.1	Q13233	M3K1_HUMAN	mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase	1249	Protein kinase. {ECO:0000255|PROSITE- ProRule:PRU00159}.				activation of MAPKK activity (GO:0000186)|apoptotic mitochondrial changes (GO:0008637)|cellular response to mechanical stimulus (GO:0071260)|epithelial cell morphogenesis (GO:0003382)|eyelid development in camera-type eye (GO:0061029)|Fc-epsilon receptor signaling pathway (GO:0038095)|innate immune response (GO:0045087)|MyD88-dependent toll-like receptor signaling pathway (GO:0002755)|positive regulation of actin filament polymerization (GO:0030838)|protein phosphorylation (GO:0006468)|regulation of cell migration (GO:0030334)|toll-like receptor 10 signaling pathway (GO:0034166)|toll-like receptor 2 signaling pathway (GO:0034134)|toll-like receptor 4 signaling pathway (GO:0034142)|toll-like receptor 5 signaling pathway (GO:0034146)|toll-like receptor 9 signaling pathway (GO:0034162)|toll-like receptor signaling pathway (GO:0002224)|toll-like receptor TLR1:TLR2 signaling pathway (GO:0038123)|toll-like receptor TLR6:TLR2 signaling pathway (GO:0038124)|transforming growth factor beta receptor signaling pathway (GO:0007179)|wound healing (GO:0042060)	cytosol (GO:0005829)	ATP binding (GO:0005524)|JUN kinase kinase activity (GO:0008545)|MAP kinase kinase kinase activity (GO:0004709)|protein kinase activity (GO:0004672)|protein kinase binding (GO:0019901)|zinc ion binding (GO:0008270)			NS(1)|breast(19)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(8)|lung(11)|ovary(1)|skin(3)|urinary_tract(1)	57		Lung NSC(810;4.65e-05)|Prostate(74;0.0132)|Breast(144;0.0321)|Ovarian(174;0.223)		OV - Ovarian serous cystadenocarcinoma(10;6.08e-40)		AGGTCAACAGATAGGCCTTGG	0.393																																							0											0													179.0	171.0	174.0					5																	56179432		1870	4100	5970	SO:0001583	missense	0			U29671, AF042838	CCDS43318.1	5q11.2	2012-02-23	2012-02-23		ENSG00000095015	ENSG00000095015		"""Mitogen-activated protein kinase cascade / Kinase kinase kinases"""	6848	protein-coding gene	gene with protein product		600982	"""mitogen-activated protein kinase kinase kinase 1"""	MEKK1		8597633	Standard	NM_005921		Approved	MEKK, MAPKKK1	uc003jqw.4	Q13233	OTTHUMG00000059486	ENST00000399503.3:c.3745A>G	5.37:g.56179432A>G	ENSP00000382423:p.Ile1249Val			Missense_Mutation	SNP	pfam_Prot_kinase_dom,pfam_Ser-Thr/Tyr_kinase_cat_dom,superfamily_Kinase-like_dom,superfamily_ARM-type_fold,smart_Ser/Thr_dual-sp_kinase_dom,smart_Tyr_kinase_cat_dom,pfscan_Znf_RING,pfscan_Znf_SWIM,pfscan_Prot_kinase_dom	p.I1249V	ENST00000399503.3	37	c.3745	CCDS43318.1	5	.	.	.	.	.	.	.	.	.	.	A	26.0	4.696743	0.88830	.	.	ENSG00000095015	ENST00000399503	T	0.32272	1.46	5.76	5.76	0.90799	Serine/threonine-protein kinase-like domain (1);Serine/threonine-protein kinase, catalytic  domain (1);Protein kinase-like domain (1);Protein kinase, catalytic domain (1);	0.000000	0.85682	D	0.000000	T	0.50292	0.1607	M	0.62016	1.91	0.58432	D	0.999998	D	0.53885	0.963	P	0.58873	0.847	T	0.51092	-0.8749	10	0.72032	D	0.01	.	16.3786	0.83431	1.0:0.0:0.0:0.0	.	1249	Q13233	M3K1_HUMAN	V	1249	ENSP00000382423:I1249V	ENSP00000382423:I1249V	I	+	1	0	MAP3K1	56215189	1.000000	0.71417	1.000000	0.80357	0.998000	0.95712	6.258000	0.72487	2.323000	0.78572	0.528000	0.53228	ATA	0	pfam_Prot_kinase_dom,pfam_Ser-Thr/Tyr_kinase_cat_dom,superfamily_Kinase-like_dom,smart_Ser/Thr_dual-sp_kinase_dom,smart_Tyr_kinase_cat_dom,pfscan_Prot_kinase_dom		0.393	MAP3K1-001	NOVEL	basic|appris_principal|exp_conf|CCDS	protein_coding	MAP3K1	protein_coding	OTTHUMT00000132309.2	137	291	0	0.00	0	0	A	XM_042066	0	0		56179432	1	no_errors	ENST00000399503	ensembl	human	novel	74_37	missense	81	272	8.99	4.21	8	12	SNP	1	G
MAPT	4137	genome.wustl.edu	37	17	44096082	44096082	+	Missense_Mutation	SNP	G	G	A			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	G	G	G	A	G	G	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr17:44096082G>A	ENST00000571987.1	+	12	2047	c.2047G>A	c.(2047-2049)Gga>Aga	p.G683R	MAPT_ENST00000262410.5_Missense_Mutation_p.G683R|MAPT_ENST00000420682.2_Missense_Mutation_p.G337R|MAPT_ENST00000340799.5_Missense_Mutation_p.G337R|MAPT_ENST00000415613.2_Missense_Mutation_p.G701R|MAPT_ENST00000347967.5_Missense_Mutation_p.G241R|MAPT_ENST00000334239.8_Missense_Mutation_p.G277R|MAPT_ENST00000535772.1_Missense_Mutation_p.G335R|MAPT_ENST00000351559.5_Missense_Mutation_p.G366R|MAPT_ENST00000431008.3_Missense_Mutation_p.G335R|MAPT_ENST00000344290.5_Missense_Mutation_p.G701R|MAPT_ENST00000570299.1_3'UTR|MAPT_ENST00000574436.1_Missense_Mutation_p.G366R|MAPT_ENST00000446361.3_Missense_Mutation_p.G308R|MAPT_ENST00000576518.1_Missense_Mutation_p.G266R			P10636	TAU_HUMAN	microtubule-associated protein tau	683					adult walking behavior (GO:0007628)|apoptotic process (GO:0006915)|axon cargo transport (GO:0008088)|axon extension (GO:0048675)|cellular component disassembly involved in execution phase of apoptosis (GO:0006921)|generation of neurons (GO:0048699)|microtubule cytoskeleton organization (GO:0000226)|mitochondrion transport along microtubule (GO:0047497)|negative regulation of intracellular transport (GO:0032387)|neuron migration (GO:0001764)|positive regulation of axon extension (GO:0045773)|positive regulation of microtubule polymerization (GO:0031116)|regulation of autophagy (GO:0010506)|regulation of microtubule polymerization (GO:0031113)|regulation of microtubule-based movement (GO:0060632)	axon (GO:0030424)|axoneme (GO:0005930)|cytoplasmic ribonucleoprotein granule (GO:0036464)|cytosol (GO:0005829)|growth cone (GO:0030426)|microtubule (GO:0005874)|microtubule associated complex (GO:0005875)|nuclear periphery (GO:0034399)|plasma membrane (GO:0005886)|tubulin complex (GO:0045298)	apolipoprotein binding (GO:0034185)|enzyme binding (GO:0019899)|lipoprotein particle binding (GO:0071813)|microtubule binding (GO:0008017)|SH3 domain binding (GO:0017124)|structural constituent of cytoskeleton (GO:0005200)	p.G683R(1)		breast(1)|endometrium(4)|kidney(1)|large_intestine(9)|lung(14)|ovary(2)|pancreas(1)|prostate(2)|skin(1)|stomach(1)|upper_aerodigestive_tract(2)	38		Melanoma(429;0.216)			Docetaxel(DB01248)|Paclitaxel(DB01229)	CGTCCCTGGCGGAGGAAATAA	0.512																																							0											1	Substitution - Missense(1)	lung(1)											105.0	108.0	107.0					17																	44096082		2203	4300	6503	SO:0001583	missense	0			J03778	CCDS11499.1, CCDS11500.1, CCDS11501.1, CCDS11502.1, CCDS45715.1, CCDS45716.1, CCDS56033.1	17q21	2014-09-17			ENSG00000186868	ENSG00000186868			6893	protein-coding gene	gene with protein product	"""G protein beta1/gamma2 subunit-interacting factor 1"", ""microtubule-associated protein tau, isoform 4"", ""protein phosphatase 1, regulatory subunit 103"""	157140		DDPAC, MAPTL		7936241, 3131773	Standard	NM_001123067		Approved	MTBT1, tau, PPND, FTDP-17, TAU, MSTD, MTBT2, FLJ31424, MGC138549, PPP1R103	uc010dau.3	P10636	OTTHUMG00000168833	ENST00000571987.1:c.2047G>A	17.37:g.44096082G>A	ENSP00000458742:p.Gly683Arg		P18518|Q14799|Q15549|Q15550|Q15551|Q1RMF6|Q53YB1|Q5CZI7|Q5XWF0|Q6QT54|Q9UDJ3|Q9UMH0|Q9UQ96	Missense_Mutation	SNP	pfam_MAP_tubulin-bd_rpt,prints_Tau	p.G701R	ENST00000571987.1	37	c.2101	CCDS11501.1	17	.	.	.	.	.	.	.	.	.	.	G	23.3	4.397285	0.83120	.	.	ENSG00000186868	ENST00000344290;ENST00000262410;ENST00000351559;ENST00000340799;ENST00000535772;ENST00000347967;ENST00000354326;ENST00000446361;ENST00000334239;ENST00000420682;ENST00000415613;ENST00000431008	D;D;D;D;D;D;D;D;D	0.99891	-7.56;-7.56;-7.56;-7.56;-7.56;-7.56;-7.56;-7.56;-7.56	4.87	4.87	0.63330	.	0.220262	0.23887	N	0.043590	D	0.99904	0.9954	M	0.91354	3.2	0.80722	D	1	D;D;D;P;D;D;D	0.89917	0.972;0.962;0.985;0.949;0.998;1.0;0.977	P;P;P;P;D;D;P	0.97110	0.87;0.719;0.835;0.524;0.919;1.0;0.798	D	0.96111	0.9077	10	0.87932	D	0	-10.1615	16.9481	0.86235	0.0:0.0:1.0:0.0	.	701;337;284;277;308;366;683	P10636-9;P10636-7;F8WAB2;P10636-2;P10636-6;P10636-8;P10636	.;.;.;.;.;.;TAU_HUMAN	R	701;683;366;337;335;241;284;277;308;337;701;189	ENSP00000340820:G701R;ENSP00000262410:G683R;ENSP00000303214:G366R;ENSP00000340438:G337R;ENSP00000443028:G335R;ENSP00000302706:G241R;ENSP00000408975:G277R;ENSP00000413056:G337R;ENSP00000410838:G701R	ENSP00000262410:G683R	G	+	1	0	MAPT	41451929	1.000000	0.71417	0.991000	0.47740	0.798000	0.45092	9.869000	0.99810	2.408000	0.81797	0.561000	0.74099	GGA	0	pfam_MAP_tubulin-bd_rpt		0.512	MAPT-008	NOVEL	basic|appris_candidate|CCDS	protein_coding	MAPT	protein_coding	OTTHUMT00000440133.1	90	292	0	0.00	0	0	G	NM_016835	0	0		44096082	1	no_errors	ENST00000344290	ensembl	human	known	74_37	missense	85	207	8.6	5.91	8	13	SNP	1	A
CCDC67	159989	genome.wustl.edu	37	11	93097356	93097357	+	Frame_Shift_Ins	INS	-	-	G			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	-	-	-	G	-	-	Unknown	Valid	Somatic	Phase_IV	WXS	Hybrid_Capture_Illumina_Seq			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr11:93097356_93097357insG	ENST00000298050.3	+	5	428_429	c.328_329insG	c.(328-330)ctgfs	p.L110fs		NM_181645.3	NP_857596.2	Q05D60	DEUP1_HUMAN	coiled-coil domain containing 67	110					cell projection organization (GO:0030030)|de novo centriole assembly (GO:0098535)	cytoplasm (GO:0005737)|deuterosome (GO:0098536)				endometrium(3)|kidney(1)|large_intestine(1)|lung(10)|ovary(2)|skin(2)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	22		Acute lymphoblastic leukemia(157;2.35e-05)|all_hematologic(158;0.00824)				CTTTGAAAAACTGAGATTACAT	0.287																																							0											0																																										SO:0001589	frameshift_variant	0			AK058122	CCDS44707.1	11q21	2014-02-20				ENSG00000165325			26344	protein-coding gene	gene with protein product						24240477	Standard	NM_181645		Approved	FLJ25393	uc001pdq.3	Q05D60		Exception_encountered	11.37:g.93097356_93097357insG	ENSP00000298050:p.Leu110fs		Q8NEF1|Q96LL7	Frame_Shift_Ins	INS	superfamily_MHC_II-assoc_invariant_trimer	p.L110fs	ENST00000298050.3	37	c.328_329	CCDS44707.1	11																																																																																			0	superfamily_MHC_II-assoc_invariant_trimer		0.287	CCDC67-201	KNOWN	basic|appris_principal|CCDS	protein_coding	CCDC67	protein_coding		115	211	0	0.00	0	0	0	NM_181645	0	0		93097357	1	no_errors	ENST00000298050	ensembl	human	known	74_37	frame_shift_ins	89	249	11	5.32	11	14	INS	0.997:1.000	G
MT-CO2	4513	genome.wustl.edu	37	M	7980	7980	+	Missense_Mutation	SNP	A	A	G			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	A	A					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chrM:7980A>G	ENST00000361739.1	+	1	395	c.395A>G	c.(394-396)gAc>gGc	p.D132G	MT-CO3_ENST00000362079.2_5'Flank|MT-TD_ENST00000387419.1_RNA|MT-TK_ENST00000387421.1_RNA|MT-TA_ENST00000387392.1_RNA|MT-ATP6_ENST00000361899.2_5'Flank|MT-TG_ENST00000387429.1_RNA|MT-TC_ENST00000387405.1_RNA|MT-TW_ENST00000387382.1_RNA|MT-ND3_ENST00000361227.2_5'Flank|MT-ND4L_ENST00000361335.1_5'Flank|MT-TN_ENST00000387400.1_RNA|MT-TY_ENST00000387409.1_RNA|MT-TR_ENST00000387439.1_RNA|MT-ND4_ENST00000361381.2_5'Flank|MT-ATP8_ENST00000361851.1_5'Flank|MT-TS1_ENST00000387416.2_RNA			P00403	COX2_HUMAN	mitochondrially encoded cytochrome c oxidase II	132					cellular metabolic process (GO:0044237)|hydrogen ion transmembrane transport (GO:1902600)|mitochondrial electron transport, cytochrome c to oxygen (GO:0006123)|respiratory electron transport chain (GO:0022904)|small molecule metabolic process (GO:0044281)	extracellular vesicular exosome (GO:0070062)|integral component of membrane (GO:0016021)|membrane (GO:0016020)|mitochondrial inner membrane (GO:0005743)|mitochondrion (GO:0005739)|respiratory chain complex IV (GO:0045277)	copper ion binding (GO:0005507)|cytochrome-c oxidase activity (GO:0004129)			endometrium(5)|kidney(8)|lung(2)|pancreas(3)|prostate(1)	19						AGAACCAGGCGACCTGCGACT	0.473																																							0											0																																										SO:0001583	missense	0					mitochondria	2012-11-16	2005-02-15	2005-02-16	ENSG00000198712	ENSG00000198712		"""Mitochondrial respiratory chain complex / Complex IV"""	7421	protein-coding gene	gene with protein product		516040	"""cytochrome c oxidase II"""	MTCO2		1712754, 1989603	Standard			Approved	COX2, CO2		P00403		ENST00000361739.1:c.395A>G	M.37:g.7980A>G	ENSP00000354876:p.Asp132Gly		Q37526	Missense_Mutation	SNP	pfam_Cyt_c_oxidase_su2_C,pfam_Cyt_c_oxidase_su2_TM_dom,superfamily_Cupredoxin,superfamily_Cyt_c_oxidase_su2_TM_dom,pfscan_Cyt_c_oxidase_su2_TM_dom,pfscan_Cyt_c_oxidase_su2_C,tigrfam_Cyt_c_oxidase_su2	p.D132G	ENST00000361739.1	37	c.395		MT																																																																																			0	pfam_Cyt_c_oxidase_su2_C,superfamily_Cupredoxin,pfscan_Cyt_c_oxidase_su2_C,tigrfam_Cyt_c_oxidase_su2		0.473	MT-CO2-201	KNOWN	basic|appris_principal	protein_coding	MT-CO2	protein_coding		401	1	0	0.00	0	0	A	YP_003024029	0	0		7980	1	no_errors	ENST00000361739	ensembl	human	known	74_37	missense	54	6	55	0.00	66	0	SNP	NULL	G
LOC729218	729218	genome.wustl.edu	37	4	119554804	119554804	+	lincRNA	SNP	G	G	A			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	G	G					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr4:119554804G>A	ENST00000567913.2	+	0	4315																											GGCCTCTCCGGGTGCAAAAGT	0.697																																							0											0																																												0																															4.37:g.119554804G>A				RNA	SNP	0	NULL	ENST00000567913.2	37	NULL		4																																																																																			0	0		0.697	RP11-384K6.6-001	KNOWN	basic	lincRNA	LOC101929676	lincRNA	OTTHUMT00000364170.2	59	6	1.67	0.00	1	0	G		0	0		119554804	1	no_errors	ENST00000567913	ensembl	human	known	74_37	rna	23	8	14.81	0.00	4	0	SNP	0.251	A
RFX1	5989	genome.wustl.edu	37	19	14074690	14074690	+	Missense_Mutation	SNP	C	C	T			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	C	C					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr19:14074690C>T	ENST00000254325.4	-	17	2575	c.2341G>A	c.(2341-2343)Gtg>Atg	p.V781M		NM_002918.4	NP_002909.4	P22670	RFX1_HUMAN	regulatory factor X, 1 (influences HLA class II expression)	781	Necessary for dimerization.				immune response (GO:0006955)|regulation of transcription from RNA polymerase II promoter (GO:0006357)|transcription from RNA polymerase II promoter (GO:0006366)	nucleus (GO:0005634)	DNA binding (GO:0003677)|RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity (GO:0003705)			NS(1)|breast(1)|endometrium(3)|kidney(1)|large_intestine(2)|lung(8)|ovary(2)|pancreas(1)|skin(1)|upper_aerodigestive_tract(1)	21			OV - Ovarian serous cystadenocarcinoma(19;6.67e-23)			GCGAAGTCCACGCGGTTGAGG	0.716																																							0											0													32.0	17.0	22.0					19																	14074690		2106	4132	6238	SO:0001583	missense	0				CCDS12301.1	19p13.1	2008-07-17				ENSG00000132005			9982	protein-coding gene	gene with protein product	"""trans-acting regulatory factor 1"", ""enhancer factor C"", ""MHC class II regulatory factor RFX"""	600006				1505960, 8289803	Standard	NM_002918		Approved	EF-C	uc002mxv.3	P22670		ENST00000254325.4:c.2341G>A	19.37:g.14074690C>T	ENSP00000254325:p.Val781Met			Missense_Mutation	SNP	pfam_RFX1_trans_act,pfam_DNA-bd_RFX	p.V781M	ENST00000254325.4	37	c.2341	CCDS12301.1	19	.	.	.	.	.	.	.	.	.	.	c	35	5.505959	0.96371	.	.	ENSG00000132005	ENST00000254325	T	0.48836	0.8	4.86	4.86	0.63082	.	0.121727	0.53938	D	0.000044	T	0.73289	0.3568	M	0.90814	3.15	0.80722	D	1	D	0.76494	0.999	D	0.66351	0.943	T	0.79918	-0.1600	10	0.72032	D	0.01	-22.8637	16.9582	0.86265	0.0:1.0:0.0:0.0	.	781	P22670	RFX1_HUMAN	M	781	ENSP00000254325:V781M	ENSP00000254325:V781M	V	-	1	0	RFX1	13935690	1.000000	0.71417	1.000000	0.80357	0.989000	0.77384	7.599000	0.82757	2.548000	0.85928	0.543000	0.68304	GTG	0	NULL		0.716	RFX1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	RFX1	protein_coding	OTTHUMT00000458510.1	21	14	0	0.00	0	0	C	NM_002918	0	0		14074690	-1	no_errors	ENST00000254325	ensembl	human	known	74_37	missense	20	6	13.04	0.00	3	0	SNP	1	T
KRTAP10-1	386677	genome.wustl.edu	37	21	45959695	45959695	+	Silent	SNP	G	G	T			TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	G	G					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr21:45959695G>T	ENST00000400375.1	-	1	383	c.339C>A	c.(337-339)acC>acA	p.T113T	TSPEAR_ENST00000397916.1_Intron|TSPEAR_ENST00000323084.4_Intron	NM_198691.2	NP_941964.2	P60331	KR101_HUMAN	keratin associated protein 10-1	113	24 X 5 AA repeats of C-C-X(3).					keratin filament (GO:0045095)				breast(1)|central_nervous_system(1)|endometrium(1)|lung(3)|prostate(4)|skin(1)	11						CCTTAGAgcaggtgggcaggc	0.632																																							0											0													56.0	61.0	59.0					21																	45959695		2202	4294	6496	SO:0001819	synonymous_variant	0			AJ566380	CCDS42954.1	21q22.3	2007-10-05			ENSG00000215455	ENSG00000215455		"""Keratin associated proteins"""	22966	protein-coding gene	gene with protein product				KRTAP18-1			Standard	NM_198691		Approved	KAP10.1, KAP18.1	uc002zfh.1	P60331	OTTHUMG00000057627	ENST00000400375.1:c.339C>A	21.37:g.45959695G>T			Q0VAR0|Q0VAR1	Silent	SNP	NULL	p.T113	ENST00000400375.1	37	c.339	CCDS42954.1	21																																																																																			0	NULL		0.632	KRTAP10-1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	KRTAP10-1	protein_coding	OTTHUMT00000128030.1	54	5	1.82	0.00	1	0	G		0	0		45959695	-1	no_errors	ENST00000400375	ensembl	human	known	74_37	silent	37	6	9.76	0.00	4	0	SNP	0.578	T
AC026320.1	0	genome.wustl.edu	37	3	191693737	191693749	+	RNA	DEL	TCTCTCCGTGTGT	TCTCTCCGTGTGT	-	rs199865256|rs371584059		TCGA-XU-AAXZ-01A-11D-A428-09	TCGA-XU-AAXZ-10A-01D-A42B-09	TCTCTCCGTGTGT	TCTCTCCGTGTGT					Unknown	Untested	Somatic	Phase_IV	WXS	none			Illumina HiSeq	4555a0e7-efe1-45de-b2a4-3e5b1930b4b9	c3b2e9a1-8d1e-4baf-b47b-79a4df0f3abc	g.chr3:191693737_191693749delTCTCTCCGTGTGT	ENST00000401201.1	+	0	0_7																											tctctctctctctctcCgtgtgtgtgtgtgtgt	0.484																																							0											0																																												0																															3.37:g.191693737_191693749delTCTCTCCGTGTGT				RNA	DEL	0	NULL	ENST00000401201.1	37	NULL		3																																																																																			0	0		0.484	AC026320.1-201	NOVEL	basic	miRNA	ENSG00000216020	miRNA		11	0	0	0.00	0	0	TCTCTCCGTGTGT		0	0		191693749	1	no_errors	ENST00000401201	ensembl	human	novel	74_37	rna	5	0	37.5	0.00	3	0	DEL	0.003:0.003:0.000:0.000:0.000:0.000:0.000:0.000:0.000:0.000:0.000:0.000:0.000	0
