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
AMPD3	272	broad.mit.edu	37	11	10523050	10523050	+	Silent	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr11:10523050G>A	ENST00000396554.3	+	12	2123	c.1782G>A	c.(1780-1782)ccG>ccA	p.P594P	AMPD3_ENST00000530864.1_3'UTR|AMPD3_ENST00000444303.2_Silent_p.P426P	NM_000480.2	NP_000471.1	Q01432	AMPD3_HUMAN	adenosine monophosphate deaminase 3	585					AMP catabolic process|purine base metabolic process|purine ribonucleoside monophosphate biosynthetic process|purine-containing compound salvage	cytosol	AMP deaminase activity|metal ion binding			central_nervous_system(1)|endometrium(1)|kidney(1)|large_intestine(5)|lung(12)|ovary(1)|prostate(3)|skin(1)	25				all cancers(16;1.14e-08)|Epithelial(150;2.83e-08)|BRCA - Breast invasive adenocarcinoma(625;0.0291)		TGTTCCGGCCGCACTGTGGGG	0.632		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													50	42	44			NA	NA	11		NA											NA				10523050		2201	4294	6495	SO:0001819	synonymous_variant			M84722	CCDS7802.1, CCDS41617.1, CCDS44537.1, CCDS53601.1	11p15	2010-02-10	2010-02-10			ENSG00000133805	272	272	3.5.4.6		470	protein-coding gene	gene with protein product	erythrocyte-specific AMP deaminase	102772	adenosine monophosphate deaminase (isoform E)		NA	1400401	Standard	NM_000480	NM_001172430	NA	Approved		uc001min.1	Q01432		ENST00000396554.3:c.1782G>A	11.37:g.10523050G>A		NA	B7Z877	37	CCDS7802.1																																																																																			AMPD3-001	PUTATIVE	basic|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000385783.2		+	ENST00000396554.3	Silent	SNP	11 : 10523050 - 10523050 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	172	4
ANKAR	150709	broad.mit.edu	37	2	190592627	190592627	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr2:190592627G>A	ENST00000520309.1	+	13	2769	c.2681G>A	c.(2680-2682)cGt>cAt	p.R894H	ANKAR_ENST00000438402.2_Missense_Mutation_p.R894H|ANKAR_ENST00000281412.6_Missense_Mutation_p.R669H|ANKAR_ENST00000431575.2_Missense_Mutation_p.R823H|ANKAR_ENST00000313581.4_Missense_Mutation_p.R894H	NM_144708.3	NP_653309.3	Q7Z5J8	ANKAR_HUMAN	ankyrin and armadillo repeat containing	894						integral to membrane	binding	p.R823H(1)		breast(3)|central_nervous_system(2)|endometrium(5)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(7)|liver(2)|lung(16)|ovary(2)|pancreas(1)|skin(1)|urinary_tract(2)	46			OV - Ovarian serous cystadenocarcinoma(117;0.00156)|Epithelial(96;0.0256)|all cancers(119;0.0744)			GAGGTTGGGCGTGACAATAAG	0.373		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				1	Substitution - Missense(1)	large_intestine(1)											104	108	107			NA	NA	2		NA											NA				190592627		2203	4300	6503	SO:0001583	missense			AJ549812	CCDS33351.1, CCDS33351.2	2q32.2	2013-02-14			ENSG00000151687	ENSG00000151687	150709	150709		Ankyrin repeat domain containing, Armadillo repeat containing	26350	protein-coding gene	gene with protein product		609803			NA	15110750	Standard	NM_144708	NM_144708	NA	Approved	FLJ25415	uc002uqw.2	Q7Z5J8	OTTHUMG00000154398	ENST00000520309.1:c.2681G>A	2.37:g.190592627G>A	ENSP00000427882:p.Arg894His	NA	Q3ZCS6|Q4G0M2|Q6ZU02	37	CCDS33351.2	.	.	.	.	.	.	.	.	.	.	G	15.00	2.704006	0.48412	.	.	ENSG00000151687	ENST00000520309;ENST00000313581;ENST00000438402;ENST00000431575;ENST00000281412	T;T;T;T;T	0.30714	1.52;1.52;1.52;1.52;1.52	5.43	4.56	0.56223	.	0.000000	0.64402	D	0.000003	T	0.44371	0.1290	L	0.57536	1.79	0.40096	D	0.976317	.	.	.	.	.	.	T	0.46062	-0.9218	8	0.62326	D	0.03	-15.5907	13.4495	0.61163	0.0766:0.0:0.9234:0.0	.	.	.	.	H	894;894;894;823;669	ENSP00000427882:R894H;ENSP00000313513:R894H;ENSP00000397243:R894H;ENSP00000393043:R823H;ENSP00000281412:R669H	ENSP00000281412:R669H	R	+	2	0	ANKAR	190300872	1.000000	0.71417	0.174000	0.22961	0.966000	0.64601	3.995000	0.57001	1.531000	0.49152	-0.244000	0.11960	CGT	ANKAR-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000335045.3		+	ENST00000520309.1	Missense_Mutation	SNP	2 : 190592627 - 190592627 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	336	7
BIRC6	57448	broad.mit.edu	37	2	32706462	32706462	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr2:32706462G>A	ENST00000421745.2	+	38	7617	c.7483G>A	c.(7483-7485)Gac>Aac	p.D2495N		NM_016252.3	NP_057336	Q9NR09	BIRC6_HUMAN	baculoviral IAP repeat containing 6	2495					anti-apoptosis|apoptosis	intracellular	acid-amino acid ligase activity|cysteine-type endopeptidase inhibitor activity|protein binding			NS(4)|breast(8)|central_nervous_system(3)|endometrium(21)|haematopoietic_and_lymphoid_tissue(1)|kidney(15)|large_intestine(31)|lung(65)|ovary(7)|pancreas(1)|prostate(5)|skin(5)|stomach(1)|urinary_tract(5)	172	Acute lymphoblastic leukemia(172;0.155)					AATGGAAGTTGACATTGATCC	0.383		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA		Pancreas(94;175 1509 16028 18060 45422)							NA				0													85	88	87			NA	NA	2		NA											NA				32706462		2203	4300	6503	SO:0001583	missense			AF265555	CCDS33175.2	2p22.3	2011-01-25	2011-01-25		ENSG00000115760	ENSG00000115760	57448	57448		Baculoviral IAP repeat containing, Ubiquitin-conjugating enzymes E2	13516	protein-coding gene	gene with protein product	apollon	605638	baculoviral IAP repeat-containing 6		NA	10544019	Standard	NM_016252	NM_016252	NA	Approved	BRUCE	uc010ezu.3	Q9NR09	OTTHUMG00000150528	ENST00000421745.2:c.7483G>A	2.37:g.32706462G>A	ENSP00000393596:p.Asp2495Asn	NA	Q9ULD1	37	CCDS33175.2	.	.	.	.	.	.	.	.	.	.	G	20.2	3.945596	0.73672	.	.	ENSG00000115760	ENST00000421745	T	0.76839	-1.05	5.31	5.31	0.75309	.	0.059209	0.64402	D	0.000005	T	0.77877	0.4196	N	0.24115	0.695	0.53688	D	0.999977	D	0.58268	0.982	P	0.54270	0.747	T	0.81059	-0.1104	10	0.66056	D	0.02	.	18.9683	0.92706	0.0:0.0:1.0:0.0	.	2495	Q9NR09	BIRC6_HUMAN	N	2495	ENSP00000393596:D2495N	ENSP00000393596:D2495N	D	+	1	0	BIRC6	32559966	1.000000	0.71417	1.000000	0.80357	0.959000	0.62525	7.849000	0.86908	2.501000	0.84356	0.460000	0.39030	GAC	BIRC6-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000318769.3		+	ENST00000421745.2	Missense_Mutation	SNP	2 : 32706462 - 32706462 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	266	5
C1orf172	0	broad.mit.edu	37	1	27278809	27278809	+	Silent	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr1:27278809C>T	ENST00000320567.5	-	2	151	c.63G>A	c.(61-63)cgG>cgA	p.R21R		NM_152365.2	NP_689578.2	Q8NAX2	CA172_HUMAN		21	Pro-rich.									NS(1)|endometrium(2)|kidney(1)|large_intestine(3)|lung(5)|ovary(1)|prostate(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	17		all_cancers(24;1.29e-21)|all_epithelial(13;2.35e-19)|Colorectal(325;0.000147)|all_lung(284;0.00122)|Lung NSC(340;0.00128)|Breast(348;0.00131)|Renal(390;0.00211)|Myeloproliferative disorder(586;0.0393)|Ovarian(437;0.0707)|all_neural(195;0.0966)		UCEC - Uterine corpus endometrioid carcinoma (279;0.0178)|Epithelial(14;3.37e-51)|OV - Ovarian serous cystadenocarcinoma(117;2.22e-29)|Colorectal(126;5.31e-09)|COAD - Colon adenocarcinoma(152;9.31e-07)|BRCA - Breast invasive adenocarcinoma(304;0.000272)|STAD - Stomach adenocarcinoma(196;0.000588)|KIRC - Kidney renal clear cell carcinoma(1967;0.000716)|READ - Rectum adenocarcinoma(331;0.0419)		GCTCTGTTGGCCGCTCCCACG	0.647		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													33	36	35			NA	NA	1		NA											NA				27278809		2168	4233	6401	SO:0001819	synonymous_variant											NA	NA			NA							NA					NA						ENST00000320567.5:c.63G>A	1.37:g.27278809C>T		NA	Q5QP32|Q8N0S7	37	CCDS293.1																																																																																			C1orf172-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000012340.1		-	ENST00000320567.5	Silent	SNP	1 : 27278809 - 27278809 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	279	5
DHRS7	51635	broad.mit.edu	37	14	60620745	60620745	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr14:60620745G>A	ENST00000216500.5	-	4	780	c.325C>T	c.(325-327)Ccc>Tcc	p.P109S	DHRS7_ENST00000536410.2_Missense_Mutation_p.P59S|PCNXL4_ENST00000406949.1_Intron|PCNXL4_ENST00000553898.1_Intron|DHRS7_ENST00000557185.1_Missense_Mutation_p.P109S			Q9Y394	DHRS7_HUMAN	dehydrogenase/reductase (SDR family) member 7	109							binding|oxidoreductase activity			endometrium(1)|lung(1)|ovary(1)|prostate(1)|urinary_tract(1)	5				OV - Ovarian serous cystadenocarcinoma(108;0.121)		AGGTCAAGGGGCAAAACAAGT	0.398		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0								G	SER/PRO	0,4406		0,0,2203	102	105	104		325	6.2	1	14		104	1,8599	1.2+/-3.3	0,1,4299	no	missense	DHRS7	NM_016029.2	74	0,1,6502	AA,AG,GG	NA	0.0116,0.0,0.0077	probably-damaging	109/340	60620745	1,13005	2203	4300	6503	SO:0001583	missense			AF151844	CCDS9743.1	14q23.1	2011-09-20			ENSG00000100612	ENSG00000100612	51635	51635		Short chain dehydrogenase/reductase superfamily / Classical SDR fold cluster 3	21524	protein-coding gene	gene with protein product	retinal short-chain dehydrogenase/reductase 4, short chain dehydrogenase/reductase family 34C, member 1	612833			NA	10800688, 10810093, 19027726	Standard	NM_016029	NM_016029	NA	Approved	retDSR4, SDR34C1	uc001xes.3	Q9Y394	OTTHUMG00000140331	ENST00000216500.5:c.325C>T	14.37:g.60620745G>A	ENSP00000216500:p.Pro109Ser	NA	B2R896|Q9UKU2	37	CCDS9743.1	.	.	.	.	.	.	.	.	.	.	G	24.5	4.535731	0.85812	0.0	1.16E-4	ENSG00000100612	ENST00000216500;ENST00000360557;ENST00000557185;ENST00000536410	D;D;D	0.87103	-2.21;-2.21;-2.21	6.16	6.16	0.99307	NAD(P)-binding domain (1);	0.154690	0.64402	D	0.000015	D	0.90304	0.6967	L	0.28649	0.875	0.80722	D	1	D;D	0.76494	0.999;0.999	D;D	0.74348	0.945;0.983	D	0.88764	0.3259	10	0.40728	T	0.16	.	20.8598	0.99761	0.0:0.0:1.0:0.0	.	109;109	F8W9Q4;Q9Y394	.;DHRS7_HUMAN	S	109;109;109;59	ENSP00000216500:P109S;ENSP00000451882:P109S;ENSP00000442993:P59S	ENSP00000216500:P109S	P	-	1	0	DHRS7	59690498	1.000000	0.71417	1.000000	0.80357	0.563000	0.35712	9.197000	0.94985	2.937000	0.99478	0.650000	0.86243	CCC	DHRS7-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000276947.2		-	ENST00000216500.5	Missense_Mutation	SNP	14 : 60620745 - 60620745 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	293	5
DHX30	22907	broad.mit.edu	37	3	47891156	47891156	+	Silent	SNP	T	T	C			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr3:47891156T>C	ENST00000348968.4	+	22	3564	c.3144T>C	c.(3142-3144)taT>taC	p.Y1048Y	DHX30_ENST00000457607.1_Silent_p.Y1104Y|DHX30_ENST00000446256.2_Silent_p.Y1037Y|DHX30_ENST00000445061.1_Silent_p.Y1076Y			Q7L2E3	DHX30_HUMAN	DEAH (Asp-Glu-Ala-His) box helicase 30	1076						mitochondrial nucleoid	ATP binding|ATP-dependent helicase activity|protein binding|RNA binding			endometrium(3)|kidney(1)|large_intestine(11)|lung(13)|ovary(4)|pancreas(1)|prostate(1)|skin(3)	37				BRCA - Breast invasive adenocarcinoma(193;0.000696)|KIRC - Kidney renal clear cell carcinoma(197;0.00609)|Kidney(197;0.007)		GGCTGACGTATTTCATGGCAG	0.627		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													88	80	83			NA	NA	3		NA											NA				47891156		2203	4300	6503	SO:0001819	synonymous_variant			AB020697	CCDS2759.1	3p24.3-p22.1	2013-07-16	2013-07-16	2003-06-13	ENSG00000132153	ENSG00000132153	22907	22907		DEAH-boxes	16716	protein-coding gene	gene with protein product			DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 30, DEAH (Asp-Glu-Ala-His) box polypeptide 30	DDX30	NA	10048485, 18022663	Standard	NM_138615	NM_138615	NA	Approved	KIAA0890, FLJ11214	uc003cru.3	Q7L2E3	OTTHUMG00000133522	ENST00000348968.4:c.3144T>C	3.37:g.47891156T>C		NA	A8K5F1|O94965|Q7Z753|Q96CH4|Q9NUQ0	37																																																																																				DHX30-005	NOVEL	not_organism_supported|basic|exp_conf	protein_coding	NA	protein_coding	OTTHUMT00000346137.1		+	ENST00000348968.4	Silent	SNP	3 : 47891156 - 47891156 C PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	316	16
DNAH3	55567	broad.mit.edu	37	16	21051256	21051256	+	Missense_Mutation	SNP	G	G	A	rs141534193	byFrequency	TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr16:21051256G>A	ENST00000261383.3	-	33	4647	c.4648C>T	c.(4648-4650)Cgg>Tgg	p.R1550W	DNAH3_ENST00000415178.1_Missense_Mutation_p.R1550W	NM_017539.1	NP_060009.1	Q8TD57	DYH3_HUMAN	dynein, axonemal, heavy chain 3	1550	AAA 1 (By similarity).				ciliary or flagellar motility|microtubule-based movement	axonemal dynein complex|cilium axoneme|cytoplasm|microtubule	ATP binding|microtubule motor activity	p.R1550W(2)		NS(3)|autonomic_ganglia(1)|breast(12)|central_nervous_system(3)|cervix(2)|endometrium(15)|haematopoietic_and_lymphoid_tissue(4)|kidney(10)|large_intestine(42)|liver(2)|lung(57)|ovary(14)|pancreas(1)|prostate(7)|skin(11)|stomach(5)|upper_aerodigestive_tract(7)|urinary_tract(6)	202				GBM - Glioblastoma multiforme(48;0.207)		GCCACTGTCCGGAACAAGGCC	0.483		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				2	Substitution - Missense(2)	lung(2)						G	TRP/ARG	0,4402		0,0,2201	116	105	109		4648	4.5	1	16	dbSNP_134	109	6,8594	5.0+/-18.6	0,6,4294	yes	missense	DNAH3	NM_017539.1	101	0,6,6495	AA,AG,GG	NA	0.0698,0.0,0.0461	probably-damaging	1550/4117	21051256	6,12996	2201	4300	6501	SO:0001583	missense			U83574	CCDS10594.1	16p12.2	2008-08-01	2006-09-04		ENSG00000158486	ENSG00000158486	55567	55567		Axonemal dyneins	2949	protein-coding gene	gene with protein product		603334	dynein, axonemal, heavy polypeptide 3		NA	9256245, 9373155	Standard	NM_017539	NM_017539	NA	Approved	Dnahc3b, DLP3, Hsadhc3, DKFZp434N074	uc010vbe.2	Q8TD57	OTTHUMG00000090677	ENST00000261383.3:c.4648C>T	16.37:g.21051256G>A	ENSP00000261383:p.Arg1550Trp	NA	O00437|O15437|O43326|Q3C0H2|Q8WUP9|Q9UEM3|Q9UEM5|Q9UG35	37	CCDS10594.1	.	.	.	.	.	.	.	.	.	.	G	21.5	4.162239	0.78226	0.0	6.98E-4	ENSG00000158486	ENST00000261383;ENST00000415178	T;T	0.15256	2.44;2.44	5.48	4.5	0.54988	ATPase, AAA+ type, core (1);	0.000000	0.64402	D	0.000001	T	0.62478	0.2431	H	0.99758	4.755	0.80722	D	1	D	0.89917	1.0	D	0.97110	1.0	T	0.79614	-0.1730	10	0.87932	D	0	.	13.3483	0.60587	0.0:0.0:0.6813:0.3187	.	1550	Q8TD57	DYH3_HUMAN	W	1550	ENSP00000261383:R1550W;ENSP00000394245:R1550W	ENSP00000261383:R1550W	R	-	1	2	DNAH3	20958757	1.000000	0.71417	1.000000	0.80357	0.991000	0.79684	3.607000	0.54102	1.351000	0.45789	0.650000	0.86243	CGG	DNAH3-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000207361.1		-	ENST00000261383.3	Missense_Mutation	SNP	16 : 21051256 - 21051256 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	326	7
DNAJB1	3337	broad.mit.edu	37	19	14627503	14627503	+	Silent	SNP	C	C	T	rs146528791		TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr19:14627503C>T	ENST00000254322.2	-	2	637	c.567G>A	c.(565-567)cgG>cgA	p.R189R	DNAJB1_ENST00000396969.4_Silent_p.R89R	NM_006145.1	NP_006136.1	P25685	DNJB1_HUMAN	DnaJ (Hsp40) homolog, subfamily B, member 1	189					chaperone cofactor-dependent protein refolding|response to unfolded protein	cytoplasm|nucleolus	heat shock protein binding|unfolded protein binding			NS(1)|breast(1)|cervix(3)|endometrium(1)|kidney(1)|lung(7)|prostate(1)|urinary_tract(1)	16				GBM - Glioblastoma multiforme(1328;0.0476)		CGGGGTTTAGCCGCTTGTGGG	0.493		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													165	165	165			NA	NA	19		NA											NA				14627503		2203	4300	6503	SO:0001819	synonymous_variant			D49547	CCDS12312.1, CCDS74295.1	19p13.12	2014-08-12			ENSG00000132002	ENSG00000132002	3337	3337		Heat shock proteins / DNAJ (HSP40)	5270	protein-coding gene	gene with protein product	radial spoke 16 homolog B (Chlamydomonas)	604572		HSPF1	NA	8975727, 8250930	Standard	NM_006145	XM_006722733	NA	Approved	Hsp40, Sis1, RSPH16B	uc002myz.1	P25685	OTTHUMG00000183289	ENST00000254322.2:c.567G>A	19.37:g.14627503C>T		NA		37	CCDS12312.1																																																																																			DNAJB1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000465987.1		-	ENST00000254322.2	Silent	SNP	19 : 14627503 - 14627503 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	778	7
ERN1	2081	broad.mit.edu	37	17	62130655	62130655	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr17:62130655G>A	ENST00000433197.3	-	16	2125	c.2030C>T	c.(2029-2031)gCc>gTc	p.A677V		NM_001433.3	NP_001424.3	O75460	ERN1_HUMAN	endoplasmic reticulum to nucleus signaling 1	NA	Protein kinase.				activation of signaling protein activity involved in unfolded protein response|apoptosis|cell cycle arrest|induction of apoptosis|mRNA processing|regulation of transcription, DNA-dependent|transcription, DNA-dependent	integral to endoplasmic reticulum membrane	ATP binding|endoribonuclease activity, producing 5'-phosphomonoesters|magnesium ion binding|protein binding|protein serine/threonine kinase activity			central_nervous_system(4)|kidney(1)|lung(2)|ovary(1)|stomach(1)	9						GTGGAGGTGGGCCAGGCCCGA	0.612		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													56	62	60			NA	NA	17		NA											NA				62130655		2039	4193	6232	SO:0001583	missense			AF059198	CCDS45762.1	17q23	2011-08-12	2007-08-14			ENSG00000178607	2081	2081			3449	protein-coding gene	gene with protein product	inositol-requiring enzyme 1	604033	ER to nucleus signalling 1		NA	9637683	Standard	NM_001433	NM_001433	NA	Approved	IRE1, IRE1P	uc002jdz.2	O75460		ENST00000433197.3:c.2030C>T	17.37:g.62130655G>A	ENSP00000401445:p.Ala677Val	NA	A1L457|A8K8N8|A8MXS7|Q59EE2	37	CCDS45762.1	.	.	.	.	.	.	.	.	.	.	G	25.7	4.668806	0.88348	.	.	ENSG00000178607	ENST00000433197	T	0.67345	-0.26	5.69	5.69	0.88448	Serine/threonine-protein kinase-like domain (1);Protein kinase-like domain (1);Protein kinase, catalytic domain (1);	0.058929	0.64402	D	0.000002	T	0.62332	0.2419	L	0.42744	1.35	0.80722	D	1	P	0.44690	0.841	B	0.40864	0.342	T	0.59434	-0.7455	10	0.25751	T	0.34	-24.0047	19.8084	0.96538	0.0:0.0:1.0:0.0	.	677	O75460	ERN1_HUMAN	V	677	ENSP00000401445:A677V	ENSP00000401445:A677V	A	-	2	0	ERN1	59484387	1.000000	0.71417	0.987000	0.45799	0.964000	0.63967	7.467000	0.80930	2.687000	0.91594	0.462000	0.41574	GCC	ERN1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000443734.2		-	ENST00000433197.3	Missense_Mutation	SNP	17 : 62130655 - 62130655 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	174	4
F8	2157	broad.mit.edu	37	X	154130395	154130395	+	Missense_Mutation	SNP	G	G	A	rs137852453		TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chrX:154130395G>A	ENST00000360256.4	-	19	6246	c.6046C>T	c.(6046-6048)Cgg>Tgg	p.R2016W		NM_000132.3	NP_000123.1	P00451	FA8_HUMAN	coagulation factor VIII, procoagulant component	2016	F5/8 type A 3.|Plastocyanin-like 6.		R -> P (in HEMA; severe familial).|R -> W (in HEMA; severe/moderate/mild).		acute-phase response|blood coagulation, intrinsic pathway|cell adhesion|platelet activation|platelet degranulation	extracellular space|plasma membrane|platelet alpha granule lumen	copper ion binding|oxidoreductase activity|protein binding			NS(1)|breast(3)|central_nervous_system(1)|cervix(1)|endometrium(9)|haematopoietic_and_lymphoid_tissue(3)|kidney(6)|large_intestine(27)|liver(1)|lung(47)|ovary(5)|pancreas(3)|prostate(1)|skin(5)|upper_aerodigestive_tract(5)|urinary_tract(2)	120	all_cancers(53;7.19e-17)|all_epithelial(53;9.83e-11)|all_lung(58;6.63e-07)|Lung NSC(58;2.08e-06)|all_hematologic(71;2.45e-06)|Acute lymphoblastic leukemia(192;6.56e-05)|Breast(217;0.176)|Renal(33;0.214)				Antihemophilic Factor(DB00025)|Coagulation Factor IX(DB00100)|Drotrecogin alfa(DB00055)	CATTCCACCCGCCAAATTCCA	0.418		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0			GRCh37	CM082650|CM910144	F8	M	rs137852453						121	104	110			NA	NA	X		NA											NA				154130395		2203	4300	6503	SO:0001583	missense			M90707	CCDS35457.1, CCDS44026.1	Xq28	2014-09-17	2008-07-29		ENSG00000185010	ENSG00000185010	2157	2157			3546	protein-coding gene	gene with protein product	Factor VIIIF8B, hemophilia A	300841		F8C	NA	6438528, 3935400	Standard		NM_000132	NA	Approved	FVIII, DXS1253E, HEMA	uc004fmt.3	P00451	OTTHUMG00000022688	ENST00000360256.4:c.6046C>T	X.37:g.154130395G>A	ENSP00000353393:p.Arg2016Trp	NA	Q5HY69	37	CCDS35457.1	.	.	.	.	.	.	.	.	.	.	g	19.00	3.742748	0.69418	.	.	ENSG00000185010	ENST00000360256	D	0.99656	-6.31	5.25	3.32	0.38043	Cupredoxin (2);Multicopper oxidase, type 2 (1);	0.230205	0.37955	N	0.001866	D	0.99263	0.9743	L	0.50333	1.59	0.42866	D	0.994122	D	0.89917	1.0	D	0.91635	0.999	D	0.99075	1.0835	10	0.62326	D	0.03	-4.4738	10.5809	0.45255	0.0:0.0:0.6532:0.3468	rs28937298	2016	P00451	FA8_HUMAN	W	2016	ENSP00000353393:R2016W	ENSP00000353393:R2016W	R	-	1	2	F8	153783589	1.000000	0.71417	0.985000	0.45067	0.993000	0.82548	1.834000	0.39171	1.093000	0.41377	0.538000	0.68166	CGG	F8-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000058869.4		-	ENST00000360256.4	Missense_Mutation	SNP	X : 154130395 - 154130395 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	425	7
HNRNPCL1	343069	broad.mit.edu	37	1	12907820	12907820	+	Missense_Mutation	SNP	G	G	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr1:12907820G>T	ENST00000317869.6	-	2	548	c.323C>A	c.(322-324)tCt>tAt	p.S108Y		NM_001013631.1|NM_001136561.2|NM_001146181.1	NP_001013653.1|NP_001130033.2|NP_001139653.1			heterogeneous nuclear ribonucleoprotein C-like 1	NA										NS(1)|endometrium(3)|kidney(1)|large_intestine(5)|lung(15)|prostate(1)|skin(1)|stomach(2)	29						CAAGTCAAAAGAGGAGCCGTA	0.493		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													106	101	103			NA	NA	1		NA											NA				12907820		2203	4300	6503	SO:0001583	missense			BC002696	CCDS30591.1	1p36.21	2013-02-12		2008-04-18	ENSG00000179172	ENSG00000179172	343069	343069		RNA binding motif (RRM) containing	29295	protein-coding gene	gene with protein product				HNRPCL1	NA		Standard	NM_001013631	NM_001013631	NA	Approved			O60812	OTTHUMG00000001931	ENST00000317869.6:c.323C>A	1.37:g.12907820G>T	ENSP00000365370:p.Ser108Tyr	NA		37	CCDS30591.1	.	.	.	.	.	.	.	.	.	.	.	5.656	0.305586	0.10678	.	.	ENSG00000179172	ENST00000317869	T	0.11385	2.78	0.926	0.926	0.19430	.	0.306916	0.25091	U	0.033219	T	0.10723	0.0262	M	0.73962	2.25	0.43508	D	0.995763	P	0.37061	0.58	B	0.37601	0.254	T	0.12656	-1.0539	10	0.13470	T	0.59	.	5.218	0.15354	0.0:0.0:1.0:0.0	.	108	O60812	HNRCL_HUMAN	Y	108	ENSP00000365370:S108Y	ENSP00000365370:S108Y	S	-	2	0	HNRNPCL1	12830407	1.000000	0.71417	0.965000	0.40720	0.056000	0.15407	2.787000	0.47798	0.814000	0.34374	0.173000	0.16961	TCT	HNRNPCL1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000005462.1		-	ENST00000317869.6	Missense_Mutation	SNP	1 : 12907820 - 12907820 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	535	10
HNRNPF	3185	broad.mit.edu	37	10	43883011	43883011	+	Missense_Mutation	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr10:43883011C>T	ENST00000544000.1	-	4	729	c.322G>A	c.(322-324)Gcc>Acc	p.A108T	HNRNPF_ENST00000443950.2_Missense_Mutation_p.A108T|HNRNPF_ENST00000357065.4_Missense_Mutation_p.A108T|HNRNPF_ENST00000356053.3_Missense_Mutation_p.A108T|HNRNPF_ENST00000337970.3_Missense_Mutation_p.A108T	NM_001098207.1	NP_001091677.1	P52597	HNRPF_HUMAN	heterogeneous nuclear ribonucleoprotein F	108					regulation of RNA splicing	catalytic step 2 spliceosome|cytoplasm|heterogeneous nuclear ribonucleoprotein complex|nucleoplasm	nucleotide binding|protein binding|single-stranded RNA binding			breast(1)|endometrium(1)|kidney(1)|large_intestine(4)|lung(10)|prostate(1)|urinary_tract(1)	19						CCATCGTTGGCGCTGTCGGCA	0.522		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													160	127	138			NA	NA	10		NA											NA				43883011		2203	4300	6503	SO:0001583	missense				CCDS7204.1	10q11.21	2013-02-12		2008-04-18	ENSG00000169813	ENSG00000169813	3185	3185		RNA binding motif (RRM) containing	5039	protein-coding gene	gene with protein product		601037		HNRPF	NA	7499401	Standard		NM_001098208	NA	Approved		uc001jas.2	P52597	OTTHUMG00000018029	ENST00000544000.1:c.322G>A	10.37:g.43883011C>T	ENSP00000438061:p.Ala108Thr	NA	B3KM84|Q5T0N2|Q96AU2	37	CCDS7204.1	.	.	.	.	.	.	.	.	.	.	C	12.13	1.844871	0.32606	.	.	ENSG00000169813	ENST00000544000;ENST00000443950;ENST00000356053;ENST00000357065;ENST00000337970;ENST00000540544	T;T;T;T;T	0.29142	1.58;1.58;1.58;1.58;1.58	3.9	2.05	0.26809	.	0.162293	0.53938	N	0.000049	T	0.20740	0.0499	L	0.43923	1.385	0.49299	D	0.999776	B	0.25850	0.136	B	0.23018	0.043	T	0.05115	-1.0905	10	0.14656	T	0.56	-8.8589	8.2846	0.31922	0.0:0.798:0.0:0.202	.	108	P52597	HNRPF_HUMAN	T	108;108;108;108;108;31	ENSP00000438061:A108T;ENSP00000400433:A108T;ENSP00000348345:A108T;ENSP00000349573:A108T;ENSP00000338477:A108T	ENSP00000338477:A108T	A	-	1	0	HNRNPF	43203017	1.000000	0.71417	0.959000	0.39883	0.922000	0.55478	6.668000	0.74457	0.619000	0.30197	0.561000	0.74099	GCC	HNRNPF-202	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000047705.2		-	ENST00000544000.1	Missense_Mutation	SNP	10 : 43883011 - 43883011 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	473	6
HSPH1	10808	broad.mit.edu	37	13	31712990	31712990	+	Silent	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr13:31712990C>T	ENST00000380406.5	-	15	2349	c.2013G>A	c.(2011-2013)cgG>cgA	p.R671R	HSPH1_ENST00000380405.4_Silent_p.R668R|HSPH1_ENST00000429785.2_Silent_p.R531R|HSPH1_ENST00000445273.2_Silent_p.R714R|HSPH1_ENST00000320027.5_Silent_p.R712R			Q92598	HS105_HUMAN	heat shock 105kDa/110kDa protein 1	712					positive regulation of MHC class I biosynthetic process|positive regulation of NK T cell activation|response to unfolded protein	cytoplasm|extracellular region	ATP binding			breast(1)|cervix(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(4)|lung(7)|ovary(1)|prostate(1)|skin(1)|stomach(1)|urinary_tract(1)	27		Lung SC(185;0.0257)		all cancers(112;0.00385)|Epithelial(112;0.0328)|OV - Ovarian serous cystadenocarcinoma(117;0.0375)|GBM - Glioblastoma multiforme(144;0.125)		ACATTTTTGGCCGTTCTTCAG	0.343		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													91	90	90			NA	NA	13		NA											NA				31712990		2203	4299	6502	SO:0001819	synonymous_variant			AB003333	CCDS9340.1, CCDS66525.1, CCDS73559.1	13q12.2-q13.3	2011-09-02			ENSG00000120694	ENSG00000120694	10808	10808		Heat shock proteins / HSP70	16969	protein-coding gene	gene with protein product		610703			NA	9610721, 9931472	Standard		XM_005266236	NA	Approved	HSP105B, KIAA0201, HSP105A, NY-CO-25	uc001utj.3	Q92598	OTTHUMG00000016685	ENST00000380406.5:c.2013G>A	13.37:g.31712990C>T		NA	O95739|Q5TBM6|Q5TBM7|Q5TBM8|Q9UPC4	37																																																																																				HSPH1-201	KNOWN	basic|exp_conf	protein_coding	NA	protein_coding			-	ENST00000380406.5	Silent	SNP	13 : 31712990 - 31712990 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	640	7
IPCEF1	26034	broad.mit.edu	37	6	154489200	154489200	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr6:154489200G>A	ENST00000265198.4	-	11	1111	c.956C>T	c.(955-957)tCa>tTa	p.S319L	IPCEF1_ENST00000422970.2_Missense_Mutation_p.S320L|IPCEF1_ENST00000367220.4_Missense_Mutation_p.S320L|OPRM1_ENST00000337049.4_Intron|IPCEF1_ENST00000519344.1_Missense_Mutation_p.S291L	NM_001130700.1|NM_015553.2	NP_001124172.1|NP_056368.1			interaction protein for cytohesin exchange factors 1	NA										breast(1)|central_nervous_system(2)|endometrium(3)|large_intestine(1)|lung(3)|ovary(1)|skin(1)	12						TTGCTCTAATGATTTGTACAG	0.358		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													207	201	203			NA	NA	6		NA											NA				154489200		2203	4300	6503	SO:0001583	missense			AB007863	CCDS5245.1, CCDS47509.1	6q25.2	2013-01-10			ENSG00000074706	ENSG00000074706	26034	26034		Pleckstrin homology (PH) domain containing	21204	protein-coding gene	gene with protein product	phosphoinositide binding protein PIP3-E				NA	11804589, 19756519	Standard	NM_001130699	NM_001130699	NA	Approved	PIP3-E, KIAA0403	uc021zhc.1	Q8WWN9	OTTHUMG00000015872	ENST00000265198.4:c.956C>T	6.37:g.154489200G>A	ENSP00000265198:p.Ser319Leu	NA		37	CCDS5245.1	.	.	.	.	.	.	.	.	.	.	G	20.9	4.068581	0.76301	.	.	ENSG00000074706	ENST00000265198;ENST00000422970;ENST00000367220;ENST00000519344	T;T;T;T	0.15718	2.4;2.4;2.4;2.42	5.57	5.57	0.84162	.	0.130451	0.52532	D	0.000063	T	0.31104	0.0786	M	0.67953	2.075	0.27301	N	0.957577	D;D;D	0.76494	0.997;0.999;0.999	P;D;D	0.71656	0.882;0.973;0.974	T	0.05370	-1.0889	10	0.46703	T	0.11	-17.5544	19.5657	0.95391	0.0:0.0:1.0:0.0	.	319;320;291	Q8WWN9;Q8WWN9-2;G3V132	ICEF1_HUMAN;.;.	L	319;320;320;291	ENSP00000265198:S319L;ENSP00000394751:S320L;ENSP00000356189:S320L;ENSP00000430287:S291L	ENSP00000265198:S319L	S	-	2	0	IPCEF1	154530892	1.000000	0.71417	0.953000	0.39169	0.716000	0.41182	5.784000	0.68990	2.630000	0.89119	0.591000	0.81541	TCA	IPCEF1-001	KNOWN	basic|appris_candidate|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000042789.2		-	ENST00000265198.4	Missense_Mutation	SNP	6 : 154489200 - 154489200 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	1366	17
IRF8	3394	broad.mit.edu	37	16	85942713	85942713	+	Missense_Mutation	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr16:85942713C>T	ENST00000268638.5	+	3	714	c.292C>T	c.(292-294)Cgg>Tgg	p.R98W	IRF8_ENST00000563180.1_Missense_Mutation_p.R98W	NM_002163.2	NP_002154.1	Q02556	IRF8_HUMAN	interferon regulatory factor 8	98					interferon-gamma-mediated signaling pathway|negative regulation of transcription from RNA polymerase II promoter|type I interferon-mediated signaling pathway	nucleus	DNA binding|sequence-specific enhancer binding RNA polymerase II transcription factor activity			breast(2)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(5)|large_intestine(2)|lung(8)|ovary(2)|prostate(1)|urinary_tract(1)	24		Prostate(104;0.0771)				AGTGACGGACCGGTCCCAACT	0.458		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													64	63	64			NA	NA	16		NA											NA				85942713		2198	4300	6498	SO:0001583	missense			M91196	CCDS10956.1	16q24.1	2014-09-17	2004-11-12	2004-11-12	ENSG00000140968	ENSG00000140968	3394	3394			5358	protein-coding gene	gene with protein product		601565	interferon consensus sequence binding protein 1	ICSBP1	NA	1460054, 11997525	Standard	NM_002163	NM_002163	NA	Approved	IRF-8, ICSBP	uc002fjh.3	Q02556	OTTHUMG00000137648	ENST00000268638.5:c.292C>T	16.37:g.85942713C>T	ENSP00000268638:p.Arg98Trp	NA	A0AV82	37	CCDS10956.1	.	.	.	.	.	.	.	.	.	.	C	20.3	3.969719	0.74246	.	.	ENSG00000140968	ENST00000268638	D	0.98028	-4.67	4.97	4.97	0.65823	Winged helix-turn-helix transcription repressor DNA-binding (1);Interferon regulatory factor DNA-binding domain (3);	0.125725	0.53938	D	0.000052	D	0.98723	0.9571	M	0.88570	2.965	0.80722	D	1	D;D	0.89917	1.0;1.0	D;D	0.97110	1.0;0.999	D	0.99201	1.0873	10	0.72032	D	0.01	-33.9604	12.8225	0.57700	0.2736:0.7264:0.0:0.0	.	98;98	B2R8V7;Q02556	.;IRF8_HUMAN	W	98	ENSP00000268638:R98W	ENSP00000268638:R98W	R	+	1	2	IRF8	84500214	1.000000	0.71417	1.000000	0.80357	0.996000	0.88848	2.266000	0.43320	2.485000	0.83878	0.555000	0.69702	CGG	IRF8-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000269100.2		+	ENST00000268638.5	Missense_Mutation	SNP	16 : 85942713 - 85942713 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	306	6
KCNK5	8645	broad.mit.edu	37	6	39162508	39162508	+	Silent	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr6:39162508G>A	ENST00000359534.3	-	3	665	c.327C>T	c.(325-327)ccC>ccT	p.P109P		NM_003740.3	NP_003731.1	O95279	KCNK5_HUMAN	potassium channel, subfamily K, member 5	109					excretion	integral to plasma membrane	potassium channel activity|voltage-gated ion channel activity			central_nervous_system(1)|endometrium(2)|kidney(3)|large_intestine(6)|lung(4)|skin(3)	19						GGCGACCGGCGGGGGTCTTGG	0.592		NA											g	1	5e-04	NA	0.0028	2184	NA	1	,	,	NA	2e-04	NA	NA	NA	5e-04	0.9547	EXOME	NA	NA	5e-04	SNP								NA				0													55	66	62			NA	NA	6		NA											NA				39162508		2203	4300	6503	SO:0001819	synonymous_variant			AF084830	CCDS4841.1	6p21	2012-03-07			ENSG00000164626	ENSG00000164626	8645	8645		Potassium channels, Voltage-gated ion channels / Potassium channels, Two-P	6280	protein-coding gene	gene with protein product		603493			NA	9812978, 16382106	Standard	NM_003740	XM_005249456	NA	Approved	K2p5.1, TASK-2	uc003oon.3	O95279	OTTHUMG00000014642	ENST00000359534.3:c.327C>T	6.37:g.39162508G>A		NA	B5TJL2|Q5VV76	37	CCDS4841.1																																																																																			KCNK5-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000040449.1		-	ENST00000359534.3	Silent	SNP	6 : 39162508 - 39162508 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	368	8
KRAS	3845	broad.mit.edu	37	12	25398284	25398284	+	Missense_Mutation	SNP	C	C	A	rs121913529		TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr12:25398284C>A	ENST00000311936.3	-	2	226	c.35G>T	c.(34-36)gGt>gTt	p.G12V	KRAS_ENST00000557334.1_Missense_Mutation_p.G12V|KRAS_ENST00000556131.1_Missense_Mutation_p.G12V|KRAS_ENST00000256078.4_Missense_Mutation_p.G12V	NM_004985.3	NP_004976.2	P01116	RASK_HUMAN	Kirsten rat sarcoma viral oncogene homolog	12			G -> A (in a colorectal cancer sample; somatic mutation).|G -> C (in lung carcinoma; somatic mutation).|G -> D (in pancreatic carcinoma, GASC and lung carcinoma; somatic mutation).|G -> R (in lung cancer and bladder cancer; somatic mutation).|G -> S (in lung carcinoma and GASC; somatic mutation).|G -> V (in lung carcinoma, pancreatic carcinoma, colon cancer and GASC; somatic mutation).		activation of MAPKK activity|axon guidance|blood coagulation|epidermal growth factor receptor signaling pathway|insulin receptor signaling pathway|leukocyte migration|nerve growth factor receptor signaling pathway|Ras protein signal transduction	plasma membrane	GTP binding|GTPase activity|protein binding	p.G12D(8562)|p.G12V(5775)|p.G12A(1407)|p.G12F(46)|p.G12L(8)|p.G12I(4)|p.G12E(3)|p.G12W(3)|p.G12Y(2)|p.G12fs*3(1)|p.G12C(1)|p.G12N(1)	UBE2L3/KRAS(2)	NS(6)|adrenal_gland(1)|autonomic_ganglia(3)|biliary_tract(532)|bone(2)|breast(32)|central_nervous_system(14)|cervix(50)|endometrium(411)|eye(4)|gastrointestinal_tract_(site_indeterminate)(7)|genital_tract(1)|haematopoietic_and_lymphoid_tissue(385)|kidney(8)|large_intestine(15267)|liver(29)|lung(3407)|oesophagus(16)|ovary(612)|pancreas(3739)|penis(1)|peritoneum(6)|prostate(96)|salivary_gland(6)|skin(45)|small_intestine(68)|soft_tissue(88)|stomach(207)|testis(17)|thymus(5)|thyroid(159)|upper_aerodigestive_tract(68)|urinary_tract(57)	25349	all_cancers(2;1e-35)|all_epithelial(2;1.97e-38)|all_lung(3;2.1e-23)|Lung NSC(3;1.16e-22)|Acute lymphoblastic leukemia(6;0.00231)|all_hematologic(7;0.00259)|Melanoma(3;0.0301)|Colorectal(261;0.11)|Ovarian(17;0.12)		OV - Ovarian serous cystadenocarcinoma(3;1.23e-21)|Epithelial(3;1.31e-20)|all cancers(3;5.45e-18)|STAD - Stomach adenocarcinoma(2;2.68e-05)			GCCTACGCCACCAGCTCCAAC	0.348	G12A(KMS28BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|G12A(KPNSI9S_AUTONOMIC_GANGLIA)|G12A(MM1S_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|G12A(NCIH1573_LUNG)|G12A(NCIH2009_LUNG)|G12A(RERFLCAD1_LUNG)|G12A(RPMI8226_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|G12A(SW1116_LARGE_INTESTINE)|G12D(AGS_STOMACH)|G12D(ASPC1_PANCREAS)|G12D(COLO678_LARGE_INTESTINE)|G12D(HEC1A_ENDOMETRIUM)|G12D(HEC50B_ENDOMETRIUM)|G12D(HEYA8_OVARY)|G12D(HPAC_PANCREAS)|G12D(HPAFII_PANCREAS)|G12D(KARPAS620_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|G12D(KOPN8_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|G12D(KP4_PANCREAS)|G12D(L33_PANCREAS)|G12D(LS180_LARGE_INTESTINE)|G12D(LS513_LARGE_INTESTINE)|G12D(MCAS_OVARY)|G12D(PANC0203_PANCREAS)|G12D(PANC0403_PANCREAS)|G12D(PANC0504_PANCREAS)|G12D(PANC0813_PANCREAS)|G12D(PANC1_PANCREAS)|G12D(PK1_PANCREAS)|G12D(PK59_PANCREAS)|G12D(SKLU1_LUNG)|G12D(SNUC2A_LARGE_INTESTINE)|G12D(SU8686_PANCREAS)|G12D(SUIT2_PANCREAS)|G12D(SW1990_PANCREAS)|G12V(A498_KIDNEY)|G12V(CAPAN2_PANCREAS)|G12V(CFPAC1_PANCREAS)|G12V(COLO668_LUNG)|G12V(CORL23_LUNG)|G12V(DANG_PANCREAS)|G12V(HCC56_LARGE_INTESTINE)|G12V(HUPT4_PANCREAS)|G12V(KP3_PANCREAS)|G12V(LCLC97TM1_LUNG)|G12V(NCIH2444_LUNG)|G12V(NCIH441_LUNG)|G12V(NCIH727_LUNG)|G12V(PANC0327_PANCREAS)|G12V(PATU8902_PANCREAS)|G12V(PATU8988S_PANCREAS)|G12V(QGP1_PANCREAS)|G12V(RCM1_LARGE_INTESTINE)|G12V(RERFLCAD2_LUNG)|G12V(RKN_OVARY)|G12V(SH10TC_STOMACH)|G12V(SHP77_LUNG)|G12V(SNGM_ENDOMETRIUM)|G12V(SW403_LARGE_INTESTINE)|G12V(SW480_LARGE_INTESTINE)|G12V(SW620_LARGE_INTESTINE)|G12V(SW900_LUNG)|G12V(YAPC_PANCREAS)	119	Mis		pancreatic, colorectal, lung, thyroid, AML, others				Noonan syndrome;Cardiofaciocutaneous syndrome	TSP Lung(1;<1E-08)|Multiple Myeloma(2;<1E-6)				NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA		Pancreas(8;6 143 191 305 2070 2426 4376 10944 11745 26467 38091 50869)		Dom	yes		12	12p12.1	3845	v-Ki-ras2 Kirsten rat sarcoma 2 viral oncogene homolog		L, E, M, O	15813	Substitution - Missense(15812)|Deletion - Frameshift(1)	large_intestine(9453)|pancreas(3002)|lung(1512)|ovary(500)|biliary_tract(369)|endometrium(319)|haematopoietic_and_lymphoid_tissue(163)|stomach(124)|prostate(59)|thyroid(55)|small_intestine(43)|upper_aerodigestive_tract(30)|urinary_tract(30)|soft_tissue(28)|skin(27)|cervix(22)|liver(16)|breast(11)|testis(9)|oesophagus(8)|central_nervous_system(7)|peritoneum(5)|kidney(4)|eye(4)|gastrointestinal_tract_(site_indeterminate)(3)|NS(3)|thymus(3)|autonomic_ganglia(2)|salivary_gland(1)|bone(1)											91	81	85			NA	NA	12		NA											NA				25398284		2203	4300	6503	SO:0001583	missense	Familial Cancer Database	Male Turner syndrome, Pterygium Colli syndrome, incl. Noonan-like/Multiple Giant Cell Lesion syndrome; Noonan s. with multiple lentigines/LEOPARD syndrome;CFC, CFCS	BC010502	CCDS8702.1, CCDS8703.1	12p12.1	2014-09-17	2013-07-08	2005-01-24	ENSG00000133703	ENSG00000133703	3845	3845			6407	protein-coding gene	gene with protein product		190070	v-Ki-ras2 Kirsten rat sarcoma 2 viral oncogene homolog, v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog	KRAS2	NA		Standard	NM_033360	NM_004985	NA	Approved	KRAS1	uc001rgp.1	P01116		ENST00000311936.3:c.35G>T	12.37:g.25398284C>A	ENSP00000308495:p.Gly12Val	NA	A8K8Z5|B0LPF9|P01118|Q96D10	37	CCDS8702.1	.	.	.	.	.	.	.	.	.	.	C	27.2	4.808637	0.90707	.	.	ENSG00000133703	ENST00000311936;ENST00000557334;ENST00000256078;ENST00000556131	T;T;T;T	0.78707	-1.2;-1.2;-1.2;-1.2	5.68	5.68	0.88126	Small GTP-binding protein domain (1);	0.000000	0.85682	D	0.000000	D	0.90373	0.6987	M	0.90650	3.135	0.80722	D	1	D;D	0.76494	0.997;0.999	D;D	0.72625	0.969;0.978	D	0.91773	0.5429	10	0.72032	D	0.01	.	18.3719	0.90409	0.0:1.0:0.0:0.0	.	12;12	P01116-2;P01116	.;RASK_HUMAN	V	12	ENSP00000308495:G12V;ENSP00000452512:G12V;ENSP00000256078:G12V;ENSP00000451856:G12V	ENSP00000256078:G12V	G	-	2	0	KRAS	25289551	1.000000	0.71417	1.000000	0.80357	0.998000	0.95712	7.743000	0.85020	2.668000	0.90789	0.563000	0.77884	GGT	KRAS-001	KNOWN	basic|appris_candidate|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000412230.1		-	ENST00000311936.3	Missense_Mutation	SNP	12 : 25398284 - 25398284 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	0	0
NLRP2	55655	broad.mit.edu	37	19	55494521	55494521	+	Silent	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr19:55494521C>T	ENST00000543010.1	+	6	1598	c.1455C>T	c.(1453-1455)gaC>gaT	p.D485D	NLRP2_ENST00000391721.4_Silent_p.D461D|NLRP2_ENST00000538819.1_Silent_p.D461D|NLRP2_ENST00000427260.2_Silent_p.D462D|NLRP2_ENST00000263437.6_Silent_p.D482D|NLRP2_ENST00000448584.2_Silent_p.D485D|NLRP2_ENST00000537859.1_Silent_p.D463D|NLRP2_ENST00000339757.7_Silent_p.D463D	NM_001174081.1	NP_001167552.1	Q9NX02	NALP2_HUMAN	NLR family, pyrin domain containing 2	485	NACHT.				apoptosis|positive regulation of caspase activity|positive regulation of interleukin-1 beta secretion	cytoplasm	ATP binding|Pyrin domain binding			large_intestine(4)|liver(1)|ovary(1)|skin(2)|upper_aerodigestive_tract(3)	11			BRCA - Breast invasive adenocarcinoma(297;0.163)	GBM - Glioblastoma multiforme(193;0.028)		TGTTCCTGGACGGAGACATCC	0.617		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0								C	,,,	0,4406		0,0,2203	36	36	36		1455,1389,1386,1455	0.8	0	19		36	2,8592		0,2,4295	no	coding-synonymous,coding-synonymous,coding-synonymous,coding-synonymous	NLRP2	NM_001174081.1,NM_001174082.1,NM_001174083.1,NM_017852.3	,,,	0,2,6498	TT,TC,CC	NA	0.0233,0.0,0.0154	,,,	485/1063,463/1041,462/1040,485/1063	55494521	2,12998	2203	4297	6500	SO:0001819	synonymous_variant			AK000517	CCDS12913.1, CCDS54318.1, CCDS54319.1	19q13.42	2008-02-05	2006-12-08	2006-12-08	ENSG00000022556	ENSG00000022556	55655	55655		Nucleotide-binding domain and leucine rich repeat containing	22948	protein-coding gene	gene with protein product	nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 2	609364	NACHT, leucine rich repeat and PYD containing 2	NALP2	NA	12563287, 11270363	Standard	NM_017852	NM_001174081	NA	Approved	FLJ20510, PYPAF2, NBS1, PAN1, CLR19.9	uc021vbq.1	Q9NX02	OTTHUMG00000167763	ENST00000543010.1:c.1455C>T	19.37:g.55494521C>T		NA	Q53FL5|Q59G09|Q8IXT0|Q9BVN5|Q9H6G6|Q9HAV9|Q9NWK3	37	CCDS12913.1																																																																																			NLRP2-001	KNOWN	basic|appris_candidate_longest|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000396152.1		+	ENST00000543010.1	Silent	SNP	19 : 55494521 - 55494521 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	274	5
OR2G6	391211	broad.mit.edu	37	1	248685682	248685682	+	Silent	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr1:248685682G>A	ENST00000343414.4	+	1	767	c.735G>A	c.(733-735)ctG>ctA	p.L245L		NM_001013355.1	NP_001013373.1	Q5TZ20	OR2G6_HUMAN	olfactory receptor, family 2, subfamily G, member 6	245					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			NS(1)|cervix(1)|endometrium(2)|large_intestine(7)|lung(40)|ovary(3)|prostate(2)|skin(2)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	61	all_cancers(71;0.000108)|all_epithelial(71;1.03e-05)|Breast(184;0.00909)|Ovarian(71;0.0377)|all_lung(81;0.127)|Lung NSC(105;0.136)	all_cancers(173;0.0156)	OV - Ovarian serous cystadenocarcinoma(106;0.0265)			CGTCTCACCTGGTTGTGGTCA	0.438		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													116	117	117			NA	NA	1		NA											NA				248685682		2203	4300	6503	SO:0001819	synonymous_variant				CCDS31119.1	1q44	2012-08-09			ENSG00000188558	ENSG00000188558	391211	391211		GPCR / Class A : Olfactory receptors	27019	protein-coding gene	gene with protein product					NA		Standard	XM_372842	NM_001013355	NA	Approved		uc001ien.1	Q5TZ20	OTTHUMG00000040462	ENST00000343414.4:c.735G>A	1.37:g.248685682G>A		NA	B2RP33	37	CCDS31119.1																																																																																			OR2G6-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000097358.1		+	ENST00000343414.4	Silent	SNP	1 : 248685682 - 248685682 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	614	12
PCDHB6	56130	broad.mit.edu	37	5	140531966	140531966	+	Missense_Mutation	SNP	C	C	T			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr5:140531966C>T	ENST00000231136.1	+	1	2128	c.2128C>T	c.(2128-2130)Cgg>Tgg	p.R710W	PCDHB6_ENST00000543635.1_Missense_Mutation_p.R574W	NM_018939.2	NP_061762.1	Q9Y5E3	PCDB6_HUMAN	protocadherin beta 6	710					calcium-dependent cell-cell adhesion|homophilic cell adhesion|synapse assembly|synaptic transmission	integral to plasma membrane	calcium ion binding			cervix(1)|endometrium(14)|kidney(6)|large_intestine(16)|liver(1)|lung(33)|ovary(1)|pancreas(2)|prostate(1)|skin(6)|upper_aerodigestive_tract(2)|urinary_tract(1)	84			KIRC - Kidney renal clear cell carcinoma(527;0.00185)|Kidney(363;0.00339)			CGTGGCGGTGCGGCTGTGCAG	0.677		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													75	89	84			NA	NA	5		NA											NA				140531966		2198	4283	6481	SO:0001583	missense			AF152499	CCDS4248.1	5q31	2010-01-26			ENSG00000113211	ENSG00000113211	56130	56130		Cadherins / Protocadherins : Clustered	8691	other	protocadherin		606332			NA	10380929	Standard	NM_018939	NM_018939	NA	Approved	PCDH-BETA6	uc003lir.3	Q9Y5E3	OTTHUMG00000129623	ENST00000231136.1:c.2128C>T	5.37:g.140531966C>T	ENSP00000231136:p.Arg710Trp	NA		37	CCDS4248.1	.	.	.	.	.	.	.	.	.	.	C	19.28	3.796466	0.70567	.	.	ENSG00000113211	ENST00000543635;ENST00000231136	T;T	0.17054	2.3;2.3	4.55	-1.63	0.08345	.	.	.	.	.	T	0.45418	0.1341	H	0.95004	3.61	0.22050	N	0.999398	D	0.89917	1.0	D	0.78314	0.991	T	0.23190	-1.0195	9	0.87932	D	0	.	5.5847	0.17267	0.6595:0.1597:0.0938:0.087	.	710	Q9Y5E3	PCDB6_HUMAN	W	574;710	ENSP00000438466:R574W;ENSP00000231136:R710W	ENSP00000231136:R710W	R	+	1	2	PCDHB6	140512150	0.000000	0.05858	0.919000	0.36401	0.965000	0.64279	-0.041000	0.12084	0.036000	0.15547	-0.323000	0.08544	CGG	PCDHB6-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000251818.2		+	ENST00000231136.1	Missense_Mutation	SNP	5 : 140531966 - 140531966 T PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	947	8
PDCL3	79031	broad.mit.edu	37	2	101188240	101188240	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr2:101188240G>A	ENST00000264254.6	+	5	935	c.557G>A	c.(556-558)gGc>gAc	p.G186D		NM_024065.4	NP_076970.1	Q9H2J4	PDCL3_HUMAN	phosducin-like 3	186					apoptosis|interspecies interaction between organisms	cytoplasm	protein binding			endometrium(3)|large_intestine(2)|liver(1)|lung(6)	12						GTGTTTGGCGGCATGAACCTG	0.498		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													112	123	119			NA	NA	2		NA											NA				101188240		2203	4300	6503	SO:0001583	missense			AF267853	CCDS33261.1	2q12	2008-02-05			ENSG00000115539	ENSG00000115539	79031	79031			28860	protein-coding gene	gene with protein product		611678			NA		Standard	NM_024065	NM_024065	NA	Approved	VIAF1	uc002tao.2	Q9H2J4	OTTHUMG00000153141	ENST00000264254.6:c.557G>A	2.37:g.101188240G>A	ENSP00000264254:p.Gly186Asp	NA	B2RA00|Q53S68	37	CCDS33261.1	.|.	.|.	.|.	.|.	.|.	.|.	.|.	.|.	.|.	.|.	.|.	32|32	5.147325|5.147325	0.94603|0.94603	.|.	.|.	ENSG00000115539|ENSG00000115539	ENST00000450127|ENST00000264254	.|T	.|0.19250	.|2.16	4.89|4.89	4.89|4.89	0.63831|0.63831	.|Thioredoxin-like fold (2);	.|0.000000	.|0.85682	.|D	.|0.000000	T|T	0.52693|0.52693	0.1750|0.1750	M|M	0.87038|0.87038	2.855|2.855	0.80722|0.80722	D|D	1|1	.|D	.|0.52996	.|0.957	.|D	.|0.66196	.|0.942	T|T	0.62058|0.62058	-0.6934|-0.6934	5|10	.|0.87932	.|D	.|0	-20.1092|-20.1092	18.4609|18.4609	0.90737|0.90737	0.0:0.0:1.0:0.0|0.0:0.0:1.0:0.0	.|.	.|186	.|Q9H2J4	.|PDCL3_HUMAN	T|D	134|186	.|ENSP00000264254:G186D	.|ENSP00000264254:G186D	A|G	+|+	1|2	0|0	PDCL3|PDCL3	100554672|100554672	1.000000|1.000000	0.71417|0.71417	1.000000|1.000000	0.80357|0.80357	0.994000|0.994000	0.84299|0.84299	9.835000|9.835000	0.99442|0.99442	2.436000|2.436000	0.82500|0.82500	0.650000|0.650000	0.86243|0.86243	GCA|GGC	PDCL3-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000329734.1		+	ENST00000264254.6	Missense_Mutation	SNP	2 : 101188240 - 101188240 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	630	6
PJA2	9867	broad.mit.edu	37	5	108717235	108717235	+	Silent	SNP	T	T	C			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr5:108717235T>C	ENST00000361189.2	-	3	440	c.201A>G	c.(199-201)gaA>gaG	p.E67E	PJA2_ENST00000511624.1_5'UTR|PJA2_ENST00000361557.3_Silent_p.E67E	NM_014819.4	NP_055634.3	O43164	PJA2_HUMAN	praja ring finger 2, E3 ubiquitin protein ligase	67					long-term memory|regulation of protein kinase A signaling cascade	cell junction|endoplasmic reticulum membrane|Golgi membrane|postsynaptic density|postsynaptic membrane	ligase activity|protein kinase A catalytic subunit binding|protein kinase A regulatory subunit binding|zinc ion binding			endometrium(2)|kidney(2)|large_intestine(5)|lung(8)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	21		all_cancers(142;4.4e-06)|all_epithelial(76;8.17e-08)|Prostate(80;0.00676)|Lung NSC(167;0.0436)|Ovarian(225;0.0443)|all_lung(232;0.053)|Colorectal(57;0.0946)|Breast(839;0.151)		OV - Ovarian serous cystadenocarcinoma(64;3.46e-10)|Epithelial(69;6.02e-09)|COAD - Colon adenocarcinoma(37;0.224)		CATCATCTAGTTCCAACACTT	0.323		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													97	90	92			NA	NA	5		NA											NA				108717235		2202	4300	6502	SO:0001819	synonymous_variant			AB007898	CCDS4099.1	5q22.1	2013-01-09	2012-02-23	2003-06-05	ENSG00000198961	ENSG00000198961	9867	9867		RING-type (C3HC4) zinc fingers	17481	protein-coding gene	gene with protein product			ring finger protein 131, praja ring finger 2	RNF131	NA		Standard	NM_014819	NM_014819	NA	Approved	KIAA0438, Neurodap1	uc003kos.4	O43164	OTTHUMG00000128750	ENST00000361189.2:c.201A>G	5.37:g.108717235T>C		NA	A8K6U4|D3DSZ5|Q68D49|Q8N1G5	37	CCDS4099.1																																																																																			PJA2-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000250663.1		-	ENST00000361189.2	Silent	SNP	5 : 108717235 - 108717235 C PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	294	9
RAMP3	10268	broad.mit.edu	37	7	45222927	45222927	+	Silent	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr7:45222927G>A	ENST00000496212.1	+	3	363	c.363G>A	c.(361-363)ccG>ccA	p.P121P	RAMP3_ENST00000481345.1_Silent_p.P121P|RAMP3_ENST00000242249.4_Silent_p.P121P			O60896	RAMP3_HUMAN	receptor (G protein-coupled) activity modifying protein 3	121					intracellular protein transport|receptor-mediated endocytosis|regulation of G-protein coupled receptor protein signaling pathway	integral to plasma membrane|lysosome	protein transporter activity			breast(1)|endometrium(1)|large_intestine(4)|lung(4)|stomach(1)	11					Pramlintide(DB01278)	TTCTCATCCCGCTGATCGTTA	0.622		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													129	123	125			NA	NA	7		NA											NA				45222927		2203	4300	6503	SO:0001819	synonymous_variant			AJ001016	CCDS5503.1	7p13-p12	2006-11-21	2006-11-21		ENSG00000122679	ENSG00000122679	10268	10268		Receptor (G protein-coupled) activity modifying proteins	9845	protein-coding gene	gene with protein product		605155	receptor activity modifying protein 3, receptor (calcitonin) activity modifying protein 3		NA		Standard	NM_005856	NM_005856	NA	Approved		uc003tnb.3	O60896	OTTHUMG00000023729	ENST00000496212.1:c.363G>A	7.37:g.45222927G>A		NA	Q7Z2Y1	37																																																																																				RAMP3-003	PUTATIVE	basic|appris_candidate_longest|exp_conf	protein_coding	NA	protein_coding	OTTHUMT00000353707.1		+	ENST00000496212.1	Silent	SNP	7 : 45222927 - 45222927 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	636	11
RGS3	5998	broad.mit.edu	37	9	116356341	116356341	+	Missense_Mutation	SNP	C	C	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr9:116356341C>A	ENST00000462403.1	+	1	576	c.142C>A	c.(142-144)Ctc>Atc	p.L48I	RGS3_ENST00000394646.3_Intron|RGS3_ENST00000374140.2_Intron|RGS3_ENST00000350696.5_Intron|RGS3_ENST00000343817.5_Intron|RGS3_ENST00000462143.1_Intron|RGS3_ENST00000342620.5_Intron|RGS3_ENST00000374134.3_Intron	NM_144489.2	NP_652760.2	P49796	RGS3_HUMAN	regulator of G-protein signaling 3	0					inactivation of MAPK activity|regulation of G-protein coupled receptor protein signaling pathway	cytosol|nucleus|plasma membrane	GTPase activator activity|signal transducer activity			cervix(1)|endometrium(3)|kidney(5)|large_intestine(11)|lung(22)|ovary(1)|prostate(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(2)	48						TCCGCTCCCCCTCCTGGTCCC	0.622		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													90	103	99			NA	NA	9		NA											NA				116356341		2203	4300	6503	SO:0001583	missense			AF006610	CCDS6797.1, CCDS6798.1, CCDS35113.1, CCDS35114.1, CCDS43869.1, CCDS65111.1	9q32	2008-02-05	2007-08-14		ENSG00000138835	ENSG00000138835	5998	5998		Regulators of G-protein signaling	9999	protein-coding gene	gene with protein product		602189	regulator of G-protein signalling 3		NA	8602223, 11034339	Standard	NM_017790	NM_001276260	NA	Approved	C2PA, FLJ20370, PDZ-RGS3	uc004bhq.4	P49796	OTTHUMG00000021048	ENST00000462403.1:c.142C>A	9.37:g.116356341C>A	ENSP00000436168:p.Leu48Ile	NA	A6NHA0|A8K0V1|Q5VXB8|Q5VXC1|Q5VZ05|Q6ZRM5|Q8IUQ1|Q8NC47|Q8NFN4|Q8NFN5|Q8TD59|Q8TD68|Q8WXA0	37	CCDS35114.1	.	.	.	.	.	.	.	.	.	.	C	8.489	0.861597	0.17178	.	.	ENSG00000138835	ENST00000462403	T	0.61627	0.09	5.42	-1.9	0.07665	.	.	.	.	.	T	0.31918	0.0812	N	0.08118	0	0.09310	N	0.999995	B	0.02656	0.0	B	0.01281	0.0	T	0.20706	-1.0267	9	0.87932	D	0	.	5.4837	0.16737	0.0889:0.2997:0.4534:0.1579	.	48	Q5VZ06	.	I	48	ENSP00000436168:L48I	ENSP00000436168:L48I	L	+	1	0	RGS3	115396162	0.000000	0.05858	0.000000	0.03702	0.020000	0.10135	-0.902000	0.04088	-0.299000	0.08909	-0.821000	0.03111	CTC	RGS3-008	KNOWN	basic|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000055568.4		+	ENST00000462403.1	Missense_Mutation	SNP	9 : 116356341 - 116356341 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	823	18
SPATA31D1	389763	broad.mit.edu	37	9	84606551	84606551	+	Missense_Mutation	SNP	T	T	C			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr9:84606551T>C	ENST00000344803.2	+	4	1213	c.1166T>C	c.(1165-1167)tTt>tCt	p.F389S		NM_001001670.2	NP_001001670.1			SPATA31 subfamily D, member 1	NA											NA						TCTGAGGCCTTTTTAGGGGGG	0.473		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													109	96	100			NA	NA	9		NA											NA				84606551		1844	4089	5933	SO:0001583	missense				CCDS47986.1	9q21.32	2012-10-12	2012-10-12	2012-10-12	ENSG00000214929	ENSG00000214929	389763	389763			37283	protein-coding gene	gene with protein product			family with sequence similarity 75, member D1	FAM75D1	NA		Standard	NM_001001670	NM_001001670	NA	Approved	FLJ46321	uc004amn.3	Q6ZQQ2	OTTHUMG00000169122	ENST00000344803.2:c.1166T>C	9.37:g.84606551T>C	ENSP00000341988:p.Phe389Ser	NA		37	CCDS47986.1	.	.	.	.	.	.	.	.	.	.	T	0.014	-1.591898	0.00864	.	.	ENSG00000214929	ENST00000344803	T	0.04156	3.69	2.87	-2.57	0.06248	.	2.194420	0.02232	N	0.064965	T	0.01353	0.0044	N	0.00313	-1.665	0.09310	N	1	B	0.02656	0.0	B	0.01281	0.0	T	0.42224	-0.9464	10	0.19590	T	0.45	-2.0064	4.1319	0.10152	0.1638:0.4916:0.0:0.3445	.	389	Q6ZQQ2	F75D1_HUMAN	S	389	ENSP00000341988:F389S	ENSP00000341988:F389S	F	+	2	0	FAM75D1	83796371	0.000000	0.05858	0.000000	0.03702	0.001000	0.01503	-0.302000	0.08221	-0.612000	0.05701	-0.734000	0.03567	TTT	SPATA31D1-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000402325.1		+	ENST00000344803.2	Missense_Mutation	SNP	9 : 84606551 - 84606551 C PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	224	7
ZNF626	199777	broad.mit.edu	37	19	20807121	20807121	+	Missense_Mutation	SNP	G	G	A			TCGA-IB-AAUW-01A-12D-A38G-08	TCGA-IB-AAUW-10A-01D-A38J-08	G	G	-	-	G	G	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	29cf030b-07b7-46ad-afb0-d7bde31ef55c	299dc91a-7da5-4537-adb8-646b7b5b75ca	g.chr19:20807121G>A	ENST00000601440.1	-	4	1708	c.1562C>T	c.(1561-1563)cCt>cTt	p.P521L	CTC-513N18.7_ENST00000595094.1_lincRNA	NM_001076675.2	NP_001070143.1	Q68DY1	ZN626_HUMAN	zinc finger protein 626	521					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			breast(1)|endometrium(1)|lung(3)|skin(1)	6						TAAGGTGTGAGGACCGCTTGA	0.378		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	19		NA											NA				20807121		2138	4266	6404	SO:0001583	missense			BC007116	CCDS32976.1, CCDS42535.1	19p13.11	2013-01-08				ENSG00000188171	199777	199777		Zinc fingers, C2H2-type, -	30461	protein-coding gene	gene with protein product					NA	12477932	Standard	NM_145297	NM_145297	NA	Approved		uc002npb.1	Q68DY1		ENST00000601440.1:c.1562C>T	19.37:g.20807121G>A	ENSP00000469958:p.Pro521Leu	NA	Q8N8T4	37	CCDS42535.1	.	.	.	.	.	.	.	.	.	.	N	3.487	-0.104716	0.06967	.	.	ENSG00000188171	ENST00000392298;ENST00000453075	.	.	.	0.832	-0.484	0.12071	.	.	.	.	.	T	0.16557	0.0398	N	0.12746	0.255	0.09310	N	1	B	0.06786	0.001	B	0.01281	0.0	T	0.19712	-1.0297	8	0.45353	T	0.12	.	2.1362	0.03763	0.3146:0.348:0.3374:0.0	.	521	Q68DY1	ZN626_HUMAN	L	521;445	.	ENSP00000376118:P521L	P	-	2	0	ZNF626	20598961	0.000000	0.05858	0.013000	0.15412	0.013000	0.08279	-4.356000	0.00247	0.171000	0.19730	0.174000	0.16983	CCT	ZNF626-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000447845.2		-	ENST00000601440.1	Missense_Mutation	SNP	19 : 20807121 - 20807121 A PAAD-TCGA-IB-AAUW-Tumor-SM-5W7VD	404	6
