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	X1000Genome_AA	X1000Genome_AC	X1000Genome_AF	X1000Genome_AFR_AF	X1000Genome_AMR_AF	X1000Genome_AN	X1000Genome_ASN_AF	X1000Genome_AVGPOST	X1000Genome_CIEND	X1000Genome_CIPOS	X1000Genome_END	X1000Genome_ERATE	X1000Genome_EUR_AF	X1000Genome_HOMLEN	X1000Genome_HOMSEQ	X1000Genome_LDAF	X1000Genome_RSQ	X1000Genome_SNPSOURCE	X1000Genome_SVLEN	X1000Genome_SVTYPE	X1000Genome_THETA	X1000Genome_VT	ACHILLES_Lineage_Results_Top_Genes	CGC_Cancer.Germline.Mut	CGC_Cancer.Molecular.Genetics	CGC_Cancer.Somatic.Mut	CGC_Cancer.Syndrome	CGC_Chr	CGC_Chr.Band	CGC_GeneID	CGC_Name	CGC_Other.Germline.Mut	CGC_Tissue.Type	COSMIC_n_overlapping_mutations	COSMIC_overlapping_mutation_descriptions	COSMIC_overlapping_primary_sites	ClinVar_ASSEMBLY	ClinVar_HGMD_ID	ClinVar_SYM	ClinVar_TYPE	ClinVar_rs	ESP_AA	ESP_AAC	ESP_AA_AC	ESP_AA_AGE	ESP_AA_GTC	ESP_AvgAAsampleReadDepth	ESP_AvgEAsampleReadDepth	ESP_AvgSampleReadDepth	ESP_CA	ESP_CDP	ESP_CG	ESP_CP	ESP_Chromosome	ESP_DBSNP	ESP_DP	ESP_EA_AC	ESP_EA_AGE	ESP_EA_GTC	ESP_EXOME_CHIP	ESP_FG	ESP_GL	ESP_GM	ESP_GS	ESP_GTC	ESP_GTS	ESP_GWAS_PUBMED	ESP_MAF	ESP_PH	ESP_PP	ESP_Position	ESP_TAC	ESP_TotalAAsamplesCovered	ESP_TotalEAsamplesCovered	ESP_TotalSamplesCovered	Ensembl_so_accession	Ensembl_so_term	Familial_Cancer_Genes_Reference	Familial_Cancer_Genes_Synonym	HGNC_Accession.Numbers	HGNC_CCDS.IDs	HGNC_Chromosome	HGNC_Date.Modified	HGNC_Date.Name.Changed	HGNC_Date.Symbol.Changed	HGNC_Ensembl.Gene.ID	HGNC_Ensembl.ID.supplied.by.Ensembl.	HGNC_Entrez.Gene.ID	HGNC_Entrez.Gene.ID.supplied.by.NCBI.	HGNC_Enzyme.IDs	HGNC_Gene.family.description	HGNC_HGNC.ID	HGNC_Locus.Group	HGNC_Locus.Type	HGNC_Name.Synonyms	HGNC_OMIM.ID.supplied.by.NCBI.	HGNC_Previous.Names	HGNC_Previous.Symbols	HGNC_Primary.IDs	HGNC_Pubmed.IDs	HGNC_Record.Type	HGNC_RefSeq.IDs	HGNC_RefSeq.supplied.by.NCBI.	HGNC_Secondary.IDs	HGNC_Status	HGNC_Synonyms	HGNC_UCSC.ID.supplied.by.UCSC.	HGNC_UniProt.ID.supplied.by.UniProt.	HGNC_VEGA.IDs	HGVS_coding_DNA_change	HGVS_genomic_change	HGVS_protein_change	ORegAnno_bin	UniProt_alt_uniprot_accessions	build	ccds_id	dbNSFP_1000Gp1_AC	dbNSFP_1000Gp1_AF	dbNSFP_1000Gp1_AFR_AC	dbNSFP_1000Gp1_AFR_AF	dbNSFP_1000Gp1_AMR_AC	dbNSFP_1000Gp1_AMR_AF	dbNSFP_1000Gp1_ASN_AC	dbNSFP_1000Gp1_ASN_AF	dbNSFP_1000Gp1_EUR_AC	dbNSFP_1000Gp1_EUR_AF	dbNSFP_Ancestral_allele	dbNSFP_CADD_phred	dbNSFP_CADD_raw	dbNSFP_CADD_raw_rankscore	dbNSFP_ESP6500_AA_AF	dbNSFP_ESP6500_EA_AF	dbNSFP_Ensembl_geneid	dbNSFP_Ensembl_transcriptid	dbNSFP_FATHMM_pred	dbNSFP_FATHMM_rankscore	dbNSFP_FATHMM_score	dbNSFP_GERP.._NR	dbNSFP_GERP.._RS	dbNSFP_GERP.._RS_rankscore	dbNSFP_Interpro_domain	dbNSFP_LRT_Omega	dbNSFP_LRT_converted_rankscore	dbNSFP_LRT_pred	dbNSFP_LRT_score	dbNSFP_LR_pred	dbNSFP_LR_rankscore	dbNSFP_LR_score	dbNSFP_MutationAssessor_pred	dbNSFP_MutationAssessor_rankscore	dbNSFP_MutationAssessor_score	dbNSFP_MutationTaster_converted_rankscore	dbNSFP_MutationTaster_pred	dbNSFP_MutationTaster_score	dbNSFP_Polyphen2_HDIV_pred	dbNSFP_Polyphen2_HDIV_rankscore	dbNSFP_Polyphen2_HDIV_score	dbNSFP_Polyphen2_HVAR_pred	dbNSFP_Polyphen2_HVAR_rankscore	dbNSFP_Polyphen2_HVAR_score	dbNSFP_RadialSVM_pred	dbNSFP_RadialSVM_rankscore	dbNSFP_RadialSVM_score	dbNSFP_Reliability_index	dbNSFP_SIFT_converted_rankscore	dbNSFP_SIFT_pred	dbNSFP_SIFT_score	dbNSFP_SLR_test_statistic	dbNSFP_SiPhy_29way_logOdds	dbNSFP_SiPhy_29way_logOdds_rankscore	dbNSFP_SiPhy_29way_pi	dbNSFP_UniSNP_ids	dbNSFP_Uniprot_aapos	dbNSFP_Uniprot_acc	dbNSFP_Uniprot_id	dbNSFP_aaalt	dbNSFP_aapos	dbNSFP_aapos_FATHMM	dbNSFP_aapos_SIFT	dbNSFP_aaref	dbNSFP_cds_strand	dbNSFP_codonpos	dbNSFP_fold.degenerate	dbNSFP_genename	dbNSFP_hg18_pos.1.coor.	dbNSFP_phastCons100way_vertebrate	dbNSFP_phastCons100way_vertebrate_rankscore	dbNSFP_phastCons46way_placental	dbNSFP_phastCons46way_placental_rankscore	dbNSFP_phastCons46way_primate	dbNSFP_phastCons46way_primate_rankscore	dbNSFP_phyloP100way_vertebrate	dbNSFP_phyloP100way_vertebrate_rankscore	dbNSFP_phyloP46way_placental	dbNSFP_phyloP46way_placental_rankscore	dbNSFP_phyloP46way_primate	dbNSFP_phyloP46way_primate_rankscore	dbNSFP_refcodon	gencode_transcript_name	gencode_transcript_status	gencode_transcript_tags	gencode_transcript_type	gene_id	gene_type	havana_transcript	secondary_variant_classification	strand	transcript_id	variant_classification	variant_type	key	t_ref_count	t_alt_count
C5orf45	51149	broad.mit.edu	37	5	179271228	179271228	+	Splice_Site	SNP	C	C	T			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr5:179271228C>T	ENST00000518219.1	-	4	227		c.e4-1		C5orf45_ENST00000518235.1_Splice_Site|C5orf45_ENST00000403396.2_Splice_Site|C5orf45_ENST00000523084.1_Splice_Site|C5orf45_ENST00000521333.1_Splice_Site|C5orf45_ENST00000292586.6_Splice_Site|C5orf45_ENST00000376931.2_Intron|C5orf45_ENST00000520698.1_Intron			Q6NTE8	CE045_HUMAN	chromosome 5 open reading frame 45	NA										breast(2)|endometrium(2)|large_intestine(2)|lung(4)|ovary(1)|prostate(1)	12						TTCTAGAGACCTTCAGGGAAG	0.552		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													118	107	111			NA	NA	5		NA											NA				179271228		2203	4300	6503	SO:0001630	splice_region_variant				CCDS34318.1, CCDS34319.1	5q35.3	2008-07-10			ENSG00000161010	ENSG00000161010	51149	51149			30817	protein-coding gene	gene with protein product	truncated calcium binding protein				NA		Standard	NM_016175	NM_016175	NA	Approved	MGC65027, MGC78537, DKFZp686L2452, LOC51149	uc003mla.3	Q6NTE8	OTTHUMG00000163490	ENST00000518219.1:c.216-1G>A	5.37:g.179271228C>T		NA	B5MD09|Q7Z3D8|Q9BUC1|Q9UN54	37		.	.	.	.	.	.	.	.	.	.	C	10.46	1.357668	0.24598	.	.	ENSG00000161010	ENST00000403396;ENST00000518235;ENST00000518219;ENST00000292586;ENST00000521333	.	.	.	3.23	3.23	0.37069	.	.	.	.	.	.	.	.	.	.	.	0.80722	D	1	.	.	.	.	.	.	.	.	.	.	.	.	.	.	10.251	0.43368	0.0:1.0:0.0:0.0	.	.	.	.	.	-1	.	.	.	-	.	.	C5orf45	179203834	0.998000	0.40836	0.983000	0.44433	0.135000	0.20990	2.497000	0.45354	2.123000	0.65237	0.561000	0.74099	.	C5orf45-006	PUTATIVE	basic	protein_coding	NA	protein_coding	OTTHUMT00000374336.1	Intron	-	ENST00000518219.1	Splice_Site	SNP	5 : 179271228 - 179271228 T PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	321	8
MANBA	4126	broad.mit.edu	37	4	103592551	103592551	+	Missense_Mutation	SNP	G	G	A			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr4:103592551G>A	ENST00000226578.4	-	9	1216	c.1117C>T	c.(1117-1119)Cgg>Tgg	p.R373W	MANBA_ENST00000505239.1_Missense_Mutation_p.R316W	NM_005908.3	NP_005899.3	O00462	MANBA_HUMAN	mannosidase, beta A, lysosomal	373					carbohydrate metabolic process|protein modification process	lysosome	beta-mannosidase activity|cation binding			cervix(2)|endometrium(9)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(10)|lung(12)|ovary(1)|prostate(3)|skin(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	42		Hepatocellular(203;0.217)		OV - Ovarian serous cystadenocarcinoma(123;4.44e-08)		AAAAGGAGCCGTAACCTGTAG	0.348		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0								G	TRP/ARG	1,4403	2.1+/-5.4	0,1,2201	33	35	34		1117	4.6	0	4		34	0,8594		0,0,4297	no	missense	MANBA	NM_005908.3	101	0,1,6498	AA,AG,GG	NA	0.0,0.0227,0.0077	benign	373/880	103592551	1,12997	2202	4297	6499	SO:0001583	missense				CCDS3658.1	4q24	2013-09-20			ENSG00000109323	ENSG00000109323	4126	4126	3.2.1.25		6831	protein-coding gene	gene with protein product		609489			NA	7876128	Standard		NM_005908	NA	Approved		uc003hwg.3	O00462	OTTHUMG00000131123	ENST00000226578.4:c.1117C>T	4.37:g.103592551G>A	ENSP00000226578:p.Arg373Trp	NA	Q96BC3|Q9NYX9	37	CCDS3658.1	.	.	.	.	.	.	.	.	.	.	G	2.904	-0.226854	0.06022	2.27E-4	0.0	ENSG00000109323	ENST00000226578;ENST00000505239	T;T	0.80824	-1.42;-1.42	5.54	4.64	0.57946	Glycoside hydrolase, subgroup, catalytic domain (1);Glycoside hydrolase, superfamily (1);	0.657345	0.15133	N	0.278747	T	0.73257	0.3564	L	0.55834	1.745	0.09310	N	1	B;B	0.27140	0.169;0.164	B;B	0.22601	0.04;0.035	T	0.64554	-0.6380	10	0.48119	T	0.1	-6.7243	5.9882	0.19446	0.1654:0.0:0.6207:0.214	.	316;373	E9PFW2;O00462	.;MANBA_HUMAN	W	373;316	ENSP00000226578:R373W;ENSP00000427322:R316W	ENSP00000226578:R373W	R	-	1	2	MANBA	103811599	0.006000	0.16342	0.004000	0.12327	0.002000	0.02628	1.176000	0.31957	1.202000	0.43218	0.655000	0.94253	CGG	MANBA-001	KNOWN	basic|appris_candidate_longest|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000253803.2		-	ENST00000226578.4	Missense_Mutation	SNP	4 : 103592551 - 103592551 A PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	125	5
MKL1	57591	broad.mit.edu	37	22	40820376	40820376	+	Missense_Mutation	SNP	A	A	C			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	A	A	-	-	A	A	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr22:40820376A>C	ENST00000402042.1	-	8	907	c.311T>G	c.(310-312)gTg>gGg	p.V104G	MKL1_ENST00000355630.3_Missense_Mutation_p.V104G|MKL1_ENST00000407029.1_Missense_Mutation_p.V104G|MKL1_ENST00000396617.3_Missense_Mutation_p.V104G	NM_001282661.1	NP_001269590.1	Q969V6	MKL1_HUMAN	megakaryoblastic leukemia (translocation) 1	104	Mediates interaction with SCAI and ACTB (By similarity).				positive regulation of transcription from RNA polymerase II promoter|smooth muscle cell differentiation|transcription, DNA-dependent	cytoplasm|nucleus	actin monomer binding|leucine zipper domain binding|nucleic acid binding|transcription coactivator activity			breast(1)|central_nervous_system(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(3)|lung(13)|ovary(4)|skin(1)|stomach(1)|urinary_tract(1)	30						GGGATAGTTCACCTGGCCCAC	0.592		NA	T	RBM15	acute megakaryocytic leukemia									NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA				Dom	yes		22	22q13	57591	megakaryoblastic leukemia (translocation) 1		L	0													60	48	52			NA	NA	22		NA											NA				40820376		2203	4300	6503	SO:0001583	missense			AB037859	CCDS14003.1, CCDS74865.1, CCDS74866.1	22q13	2008-06-12			ENSG00000196588	ENSG00000196588	57591	57591			14334	protein-coding gene	gene with protein product	megakaryocytic acute leukemia, myocardin-related transcription factor A, basic, SAP and coiled-coil domain	606078			NA	11431691, 12019265, 14970199	Standard	NM_020831	XM_005261692	NA	Approved	KIAA1438, MAL, MRTF-A, BSAC	uc003ayw.1	Q969V6	OTTHUMG00000151146	ENST00000402042.1:c.311T>G	22.37:g.40820376A>C	ENSP00000385584:p.Val104Gly	NA	Q8TCL1|Q96SC5|Q96SC6|Q9P2B0	37		.	.	.	.	.	.	.	.	.	.	A	22.3	4.278262	0.80692	.	.	ENSG00000196588	ENST00000355630;ENST00000396617;ENST00000402042;ENST00000407029	D;D;D;D	0.99859	-7.24;-7.24;-7.24;-7.24	5.72	4.68	0.58851	.	0.144847	0.47093	D	0.000251	D	0.99746	0.9899	M	0.68317	2.08	0.80722	D	1	D;D;D	0.89917	1.0;0.999;0.999	D;D;D	0.78314	0.946;0.991;0.991	D	0.97815	1.0253	10	0.33940	T	0.23	-27.5434	12.2346	0.54508	0.8724:0.0:0.0:0.1276	.	104;104;104	B0QY83;E7ER32;Q969V6	.;.;MKL1_HUMAN	G	104	ENSP00000347847:V104G;ENSP00000379861:V104G;ENSP00000385584:V104G;ENSP00000385835:V104G	ENSP00000347847:V104G	V	-	2	0	MKL1	39150322	1.000000	0.71417	1.000000	0.80357	0.971000	0.66376	5.992000	0.70609	0.981000	0.38548	0.459000	0.35465	GTG	MKL1-002	NOVEL	basic|exp_conf	protein_coding	NA	protein_coding	OTTHUMT00000321523.1		-	ENST00000402042.1	Missense_Mutation	SNP	22 : 40820376 - 40820376 C PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	243	10
OR1E2	8388	broad.mit.edu	37	17	3336543	3336543	+	Missense_Mutation	SNP	C	C	A			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr17:3336543C>A	ENST00000248384.1	-	1	592	c.593G>T	c.(592-594)tGc>tTc	p.C198F		NM_003554.1	NP_003545.1	P47887	OR1E2_HUMAN	olfactory receptor, family 1, subfamily E, member 2	198					sensory perception of smell	integral to plasma membrane	olfactory receptor activity			endometrium(3)|large_intestine(3)|lung(3)	9						AGTGTCAGAGCAGGCCAGCTT	0.458		NA											C	1	5e-04	NA	NA	2184	NA	0.9998	,	,	NA	3e-04	0.0013	NA	NA	5e-04	0.8407	EXOME	NA	NA	0.0038	SNP								NA				0								C	PHE/CYS	1,4405	2.1+/-5.4	0,1,2202	80	72	75		593	3.1	1	17		75	0,8600		0,0,4300	no	missense	OR1E2	NM_003554.1	205	0,1,6502	AA,AC,CC	NA	0.0,0.0227,0.0077	possibly-damaging	198/324	3336543	1,13005	2203	4300	6503	SO:0001583	missense			U04686	CCDS11026.1	17p13.3	2012-08-09			ENSG00000127780	ENSG00000127780	8388	8388		GPCR / Class A : Olfactory receptors	8190	protein-coding gene	gene with protein product				OR1E4	NA	8004088, 9500546	Standard		NM_003554	NA	Approved	OR17-93, OR17-135	uc010vre.2	P47887	OTTHUMG00000090651	ENST00000248384.1:c.593G>T	17.37:g.3336543C>A	ENSP00000248384:p.Cys198Phe	NA	O43877|O95632|Q0VAD5|Q0VAD6|Q9UL13	37	CCDS11026.1	1	4.578754578754579E-4	0	0.0	0	0.0	0	0.0	1	0.0013192612137203166	C	14.27	2.484364	0.44147	2.27E-4	0.0	ENSG00000127780	ENST00000248384;ENST00000454364	T	0.00460	7.27	5.15	3.12	0.35913	GPCR, rhodopsin-like superfamily (1);	0.000000	0.64402	D	0.000002	T	0.01558	0.0050	H	0.98276	4.19	0.45580	D	0.998522	P	0.37914	0.611	P	0.45794	0.493	T	0.01516	-1.1335	10	0.87932	D	0	.	9.6207	0.39719	0.0:0.7795:0.1421:0.0785	.	198	P47887	OR1E2_HUMAN	F	198;188	ENSP00000248384:C198F	ENSP00000248384:C198F	C	-	2	0	OR1E2	3283293	0.724000	0.28038	1.000000	0.80357	0.770000	0.43624	1.786000	0.38694	0.708000	0.31955	-0.263000	0.10527	TGC	OR1E2-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000207311.1		-	ENST00000248384.1	Missense_Mutation	SNP	17 : 3336543 - 3336543 A PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	252	7
ZNF131	7690	broad.mit.edu	37	5	43161989	43161989	+	Missense_Mutation	SNP	T	T	G			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr5:43161989T>G	ENST00000509634.1	+	5	1364	c.908T>G	c.(907-909)tTt>tGt	p.F303C	ZNF131_ENST00000509156.1_Missense_Mutation_p.F337C|ZNF131_ENST00000306938.4_Missense_Mutation_p.F303C|ZNF131_ENST00000505606.2_Missense_Mutation_p.F303C|ZNF131_ENST00000399534.1_Missense_Mutation_p.F337C|ZNF131_ENST00000509931.1_Intron			P52739	ZN131_HUMAN	zinc finger protein 131	337						nucleus	DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			breast(2)|endometrium(2)|kidney(1)|lung(9)|ovary(1)|prostate(1)|urinary_tract(1)	17						GAGAAACAGTTTGACCATTTT	0.328		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													55	52	53			NA	NA	5		NA											NA				43161989		1857	4095	5952	SO:0001583	missense			U09410	CCDS43313.1	5p12	2013-01-09	2006-06-13		ENSG00000172262	ENSG00000172262	7690	7690		Zinc fingers, C2H2-type, -, BTB/POZ domain containing	12915	protein-coding gene	gene with protein product	zinc finger and BTB domain containing 35	604073	zinc finger protein 131 (clone pHZ-10)		NA		Standard	NM_003432	XM_005248359	NA	Approved	ZBTB35, pHZ-10	uc003jnk.3	P52739	OTTHUMG00000162223	ENST00000509634.1:c.908T>G	5.37:g.43161989T>G	ENSP00000421246:p.Phe303Cys	NA	B4DRL3|Q6PIF0	37	CCDS43313.1	.	.	.	.	.	.	.	.	.	.	T	19.67	3.871377	0.72065	.	.	ENSG00000172262	ENST00000509156;ENST00000306938;ENST00000399534;ENST00000505606;ENST00000509634	T;T;T;T;T	0.74842	-0.88;0.82;-0.88;0.82;0.82	5.42	5.42	0.78866	Zinc finger, C2H2-like (1);Zinc finger, C2H2 (3);Zinc finger, C2H2-type/integrase, DNA-binding (1);	0.000000	0.85682	D	0.000000	D	0.87034	0.6077	M	0.83384	2.64	0.58432	D	0.999991	D;D	0.89917	1.0;1.0	D;D	0.87578	0.998;0.997	D	0.89098	0.3487	10	0.87932	D	0	-10.2228	15.4594	0.75342	0.0:0.0:0.0:1.0	.	337;303	P52739;P52739-2	ZN131_HUMAN;.	C	337;303;337;303;303	ENSP00000426504:F337C;ENSP00000305804:F303C;ENSP00000382450:F337C;ENSP00000423945:F303C;ENSP00000421246:F303C	ENSP00000305804:F303C	F	+	2	0	ZNF131	43197746	1.000000	0.71417	1.000000	0.80357	0.997000	0.91878	7.617000	0.83032	2.058000	0.61347	0.528000	0.53228	TTT	ZNF131-011	KNOWN	alternative_5_UTR|basic|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000367984.1		+	ENST00000509634.1	Missense_Mutation	SNP	5 : 43161989 - 43161989 G PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	282	7
ZNF131	7690	broad.mit.edu	37	5	43161998	43161998	+	Missense_Mutation	SNP	T	T	C			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr5:43161998T>C	ENST00000509634.1	+	5	1373	c.917T>C	c.(916-918)tTt>tCt	p.F306S	ZNF131_ENST00000509156.1_Missense_Mutation_p.F340S|ZNF131_ENST00000306938.4_Missense_Mutation_p.F306S|ZNF131_ENST00000505606.2_Missense_Mutation_p.F306S|ZNF131_ENST00000399534.1_Missense_Mutation_p.F340S|ZNF131_ENST00000509931.1_Intron			P52739	ZN131_HUMAN	zinc finger protein 131	340						nucleus	DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			breast(2)|endometrium(2)|kidney(1)|lung(9)|ovary(1)|prostate(1)|urinary_tract(1)	17						TTTGACCATTTTGGACATTTT	0.318		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													51	48	49			NA	NA	5		NA											NA				43161998		1845	4088	5933	SO:0001583	missense			U09410	CCDS43313.1	5p12	2013-01-09	2006-06-13		ENSG00000172262	ENSG00000172262	7690	7690		Zinc fingers, C2H2-type, -, BTB/POZ domain containing	12915	protein-coding gene	gene with protein product	zinc finger and BTB domain containing 35	604073	zinc finger protein 131 (clone pHZ-10)		NA		Standard	NM_003432	XM_005248359	NA	Approved	ZBTB35, pHZ-10	uc003jnk.3	P52739	OTTHUMG00000162223	ENST00000509634.1:c.917T>C	5.37:g.43161998T>C	ENSP00000421246:p.Phe306Ser	NA	B4DRL3|Q6PIF0	37	CCDS43313.1	.	.	.	.	.	.	.	.	.	.	T	16.87	3.241611	0.58995	.	.	ENSG00000172262	ENST00000509156;ENST00000306938;ENST00000399534;ENST00000505606;ENST00000509634	T;T;T;T;T	0.72942	-0.7;0.29;-0.7;0.29;0.29	5.42	5.42	0.78866	Zinc finger, C2H2-like (1);Zinc finger, C2H2 (3);Zinc finger, C2H2-type/integrase, DNA-binding (1);	0.000000	0.85682	D	0.000000	T	0.58409	0.2120	N	0.01109	-1.01	0.54753	D	0.999986	D;D	0.76494	0.999;0.999	D;D	0.83275	0.996;0.996	T	0.62595	-0.6821	10	0.07175	T	0.84	-10.013	15.4594	0.75342	0.0:0.0:0.0:1.0	.	340;306	P52739;P52739-2	ZN131_HUMAN;.	S	340;306;340;306;306	ENSP00000426504:F340S;ENSP00000305804:F306S;ENSP00000382450:F340S;ENSP00000423945:F306S;ENSP00000421246:F306S	ENSP00000305804:F306S	F	+	2	0	ZNF131	43197755	1.000000	0.71417	1.000000	0.80357	0.994000	0.84299	7.617000	0.83032	2.058000	0.61347	0.528000	0.53228	TTT	ZNF131-011	KNOWN	alternative_5_UTR|basic|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000367984.1		+	ENST00000509634.1	Missense_Mutation	SNP	5 : 43161998 - 43161998 C PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	270	7
ZSCAN5B	342933	broad.mit.edu	37	19	56701712	56701712	+	Silent	SNP	T	T	C			TCGA-HZ-7920-01A-11D-2201-08	TCGA-HZ-7920-10B-01D-2201-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	c9b48534-d832-41b4-b67a-d8f4b44d24f1	f34639f3-59c0-430e-9ae0-1eef76fe86aa	g.chr19:56701712T>C	ENST00000586855.2	-	5	1285	c.972A>G	c.(970-972)ccA>ccG	p.P324P	ZSCAN5B_ENST00000358992.3_Silent_p.P324P			A6NJL1	ZSA5B_HUMAN	zinc finger and SCAN domain containing 5B	324					viral reproduction	nucleus	DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			breast(1)|endometrium(5)|large_intestine(3)|lung(23)|ovary(1)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)	37						CAGCTTGTCCTGGGGATTCTC	0.567		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0								C		3,4403	824.6+/-416.5	0,3,2200	114	116	115		972	-1.9	0	19		115	0,8600		0,0,4300	no	coding-synonymous	ZSCAN5B	NM_001080456.2		0,3,6500	CC,CT,TT	NA	0.0,0.0681,0.0231		324/496	56701712	3,13003	2203	4300	6503	SO:0001819	synonymous_variant				CCDS46203.1	19q13.42	2013-01-08			ENSG00000197213	ENSG00000197213	342933	342933		-, Zinc fingers, C2H2-type	34246	protein-coding gene	gene with protein product					NA		Standard	NM_001080456	NM_001080456	NA	Approved	ZNF495B, ZNF371	uc010ygh.2	A6NJL1		ENST00000586855.2:c.972A>G	19.37:g.56701712T>C		NA		37	CCDS46203.1																																																																																			ZSCAN5B-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000457834.2		-	ENST00000586855.2	Silent	SNP	19 : 56701712 - 56701712 C PAAD-TCGA-HZ-7920-Tumor-SM-2RBJV	625	11
