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	validation_method	t_ref_count	validation_status	validation_tumor_sample	t_alt_count	validation_alt_allele	pox	qox	pox_cutoff	isArtifactMode	oxoGCut
MRGPRX3	117195	broad.mit.edu	37	11	18159150	18159150	+	Missense_Mutation	SNP	G	A	A	rs139790666	by1000genomes	TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr11:18159150G>A	uc021qek.1	+	0	401	c.401G>A	c.(400-402)cGc>cAc	p.R134H	MRGPRX3_uc001mnu.3_Missense_Mutation_p.R134H	NM_054031	NP_473372	Q96LB0	MRGX3_HUMAN	Homo sapiens MAS-related GPR, member X3 (MRGPRX3), mRNA.	134						integral to membrane|plasma membrane	G-protein coupled receptor activity			NS(1)|breast(2)|endometrium(2)|kidney(1)|large_intestine(5)|lung(10)|ovary(1)|pancreas(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(2)	27						CACTGCCGCCGCCCCAGATAC	0.572000														34			39		0	0	1	0	0
CACNA1C	775	broad.mit.edu	37	12	2783696	2783696	+	Silent	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr12:2783696C>T	uc009zdw.1	+	38	5152	c.4839C>T	c.(4837-4839)ttC>ttT	p.F1613F	CACNA1C_uc001qkc.2_Silent_p.F1591F|CACNA1C_uc001qjz.2_Intron|CACNA1C_uc001qkd.2_Silent_p.F1591F|CACNA1C_uc001qke.2_Intron|CACNA1C_uc001qkf.2_Silent_p.F1580F|CACNA1C_uc001qkg.2_Silent_p.F1578F|CACNA1C_uc001qkh.2_Silent_p.F1580F|CACNA1C_uc001qkl.2_Intron|CACNA1C_uc001qkj.2_Intron|CACNA1C_uc001qkk.2_Intron|CACNA1C_uc001qkn.2_Intron|CACNA1C_uc001qkm.2_Intron|CACNA1C_uc001qko.2_Intron|CACNA1C_uc001qkp.2_Intron|CACNA1C_uc001qkq.2_Intron|CACNA1C_uc001qku.2_Intron|CACNA1C_uc001qkr.2_Intron|CACNA1C_uc001qks.2_Intron|CACNA1C_uc001qkt.2_Silent_p.F1591F|CACNA1C_uc009zdu.1_Intron|CACNA1C_uc009zdv.1_Intron|CACNA1C_uc001qkb.2_Intron|CACNA1C_uc001qki.1_Intron|CACNA1C_uc010sea.1_Intron	NM_001129829	NP_001123301	Q13936	CAC1C_HUMAN	Homo sapiens calcium channel, voltage-dependent, L type, alpha 1C subunit (CACNA1C), transcript variant 3, mRNA.	1623					axon guidance|calcium ion transport into cytosol|energy reserve metabolic process|regulation of insulin secretion	cytoplasm|postsynaptic density|voltage-gated calcium channel complex	calmodulin binding|voltage-gated calcium channel activity			NS(3)|breast(4)|central_nervous_system(4)|cervix(2)|endometrium(12)|kidney(9)|large_intestine(20)|lung(55)|ovary(10)|pancreas(1)|prostate(5)|skin(3)|upper_aerodigestive_tract(4)	132			OV - Ovarian serous cystadenocarcinoma(31;0.00256)	LUAD - Lung adenocarcinoma(1;0.134)	Ibutilide(DB00308)|Isradipine(DB00270)|Magnesium Sulfate(DB00653)|Mibefradil(DB01388)|Nicardipine(DB00622)|Verapamil(DB00661)	AGGATCCTTTCCGCCCTGCAG	0.602000														52			45		0	0	1	0	0
MGC39584	441058	broad.mit.edu	37	GL000193.1	88251	88251	+	RNA	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chrGL000193.1:88251C>T	uc003izx.3	-	0		c.125G>A			MGC39584_uc003izy.3_5'Flank					Homo sapiens uncharacterized LOC441058 (MGC39584), non-coding RNA.																		gtgctgcttcccccgtctccg	0.622000														15			3		0	0	1	0	0
SOX13	9580	broad.mit.edu	37	1	204092909	204092909	+	Missense_Mutation	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr1:204092909A>G	uc001ham.3	+	11	1947	c.1352A>G	c.(1351-1353)aAc>aGc	p.N451S	SOX13_uc010pqp.2_Missense_Mutation_p.N450S|SOX13_uc010pqq.2_Missense_Mutation_p.N318S	NM_005686	NP_005677	Q9UN79	SOX13_HUMAN	Homo sapiens SRY (sex determining region Y)-box 13 (SOX13), mRNA.	451					anatomical structure morphogenesis	nucleus	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity			breast(1)|central_nervous_system(1)|endometrium(2)|large_intestine(3)|lung(2)|ovary(2)|prostate(2)	13	all_cancers(21;0.0754)|Breast(84;0.116)|all_epithelial(62;0.189)		KIRC - Kidney renal clear cell carcinoma(13;0.0584)|Kidney(21;0.0934)|BRCA - Breast invasive adenocarcinoma(75;0.109)			GACATGCACAACTCCAGCATC	0.572000											OREG0014126	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)		18			3		0	0	1	0	0
SCARA5	286133	broad.mit.edu	37	8	27779572	27779572	+	Silent	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr8:27779572G>A	uc003xgj.3	-	3	1043	c.432C>T	c.(430-432)ggC>ggT	p.G144G	SCARA5_uc010luz.3_Intron|SCARA5_uc003xgk.3_Silent_p.G101G|SCARA5_uc003xgl.3_Silent_p.G144G	NM_173833	NP_776194	Q6ZMJ2	SCAR5_HUMAN	Homo sapiens scavenger receptor class A, member 5 (putative) (SCARA5), mRNA.	144					cellular iron ion homeostasis|endocytosis|iron ion transmembrane transport|protein homotrimerization	integral to plasma membrane	ferritin receptor activity|scavenger receptor activity			central_nervous_system(1)|large_intestine(6)|lung(5)|prostate(3)|skin(3)	18		Ovarian(32;0.0218)		UCEC - Uterine corpus endometrioid carcinoma (27;0.023)|KIRC - Kidney renal clear cell carcinoma(542;0.152)|Kidney(114;0.181)|Colorectal(74;0.228)		GCTGCACTGCGCCCGCCAGCG	0.726000														7			12		0	0	1	0	0
SREK1IP1	285672	broad.mit.edu	37	5	64023984	64023984	+	Missense_Mutation	SNP	C	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr5:64023984C>A	uc003jtk.3	-	3	380	c.228G>T	c.(226-228)aaG>aaT	p.K76N		NM_173829	NP_776190	Q8N9Q2	SR1IP_HUMAN	Homo sapiens SREK1-interacting protein 1 (SREK1IP1), mRNA.	76	Lys-rich.				RNA splicing|mRNA processing		nucleic acid binding|zinc ion binding			breast(1)|endometrium(1)|large_intestine(3)|ovary(1)	6						tttctttcttcttttcctctt	0.274000														133			12		3.27435e-08	3.27435e-08	1	1	0
PCDHAC2	56134	broad.mit.edu	37	5	140221819	140221819	+	Missense_Mutation	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr5:140221819C>T	uc003lhs.2	+	0	913	c.913C>T	c.(913-915)Cgg>Tgg	p.R305W	PCDHAC2_uc003lha.2_Intron|PCDHAC2_uc003lhb.2_Intron|PCDHAC2_uc003lhd.2_Intron|PCDHAC2_uc003lhf.2_Intron|PCDHAC2_uc003lhh.1_Intron|PCDHAC2_uc003lhi.2_Intron|PCDHAC2_uc003lhl.2_Intron|PCDHAC2_uc003lhk.1_Intron|PCDHAC2_uc003lho.2_Intron|PCDHAC2_uc003lhn.2_Intron|PCDHAC2_uc003lhq.2_Intron|PCDHAC2_uc003lhr.1_Missense_Mutation_p.R305W	NM_018911	NP_061734	Q9Y5I4	PCDC2_HUMAN	Homo sapiens protocadherin alpha 8 (PCDHA8), transcript variant 1, mRNA.	320	Cadherin 3.				homophilic cell adhesion|nervous system development	integral to plasma membrane	calcium ion binding			NS(1)|breast(1)|endometrium(4)|kidney(4)|large_intestine(10)|liver(2)|lung(9)|ovary(2)|prostate(1)|skin(7)|upper_aerodigestive_tract(3)|urinary_tract(1)	45			KIRC - Kidney renal clear cell carcinoma(527;0.00112)|Kidney(363;0.00191)			AATAGTGATTCGGGGTAATTT	0.408000														220			5		0	0	1	0	0
ITGA9	3680	broad.mit.edu	37	3	37523097	37523097	+	Splice_Site	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr3:37523097A>G	uc003chd.3	+	4	597	c.544_splice	c.e4+1	p.E182_splice	ITGA9_uc003chc.3_Splice_Site_p.E182_splice	NM_002207	NP_002198	Q13797	ITA9_HUMAN	Homo sapiens integrin, alpha 9 (ITGA9), mRNA.	182					axon guidance|cell adhesion|integrin-mediated signaling pathway	integrin complex	receptor activity			breast(3)|central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(9)|lung(17)|pancreas(1)|prostate(2)|skin(6)|stomach(1)|urinary_tract(1)	44				KIRC - Kidney renal clear cell carcinoma(284;0.165)|Kidney(284;0.197)		CTTGCTATGAAGGTGAGCATG	0.542000														88			4		0	0	1	0	0
FKBP9	11328	broad.mit.edu	37	7	33028128	33028128	+	Silent	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr7:33028128G>A	uc011kal.2	+	6	1243	c.1062G>A	c.(1060-1062)cgG>cgA	p.R354R	AVL9_uc011kai.2_Intron|FKBP9_uc011kak.1_Non-coding_Transcript|FKBP9_uc003tdh.3_Silent_p.R301R|FKBP9_uc011kam.2_Silent_p.R69R	NM_007270	NP_009201	O95302	FKBP9_HUMAN	Homo sapiens FK506 binding protein 9, 63 kDa (FKBP9), mRNA.	301	PPIase FKBP-type 3.				protein folding	endoplasmic reticulum|membrane	FK506 binding|calcium ion binding|peptidyl-prolyl cis-trans isomerase activity			central_nervous_system(13)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(6)|lung(9)|ovary(2)|upper_aerodigestive_tract(1)	39			GBM - Glioblastoma multiforme(11;0.0156)			GCTACTCTCGGAACCGCACGT	0.483000														32			24		0	0	1	0	0
TOP1	7150	broad.mit.edu	37	20	39708803	39708803	+	Silent	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr20:39708803A>G	uc002xjl.3	+	5	660	c.414A>G	c.(412-414)agA>agG	p.R138R	TOP1_uc010gge.1_Non-coding_Transcript	NM_003286	NP_003277	P11387	TOP1_HUMAN	Homo sapiens topoisomerase (DNA) I (TOP1), mRNA.	138	Lys-rich.				DNA topological change|interspecies interaction between organisms|phosphorylation|programmed cell death|response to drug	chromosome|nucleolus|nucleoplasm	ATP binding|DNA topoisomerase (ATP-hydrolyzing) activity|DNA topoisomerase type I activity|chromatin DNA binding|protein binding			breast(5)|central_nervous_system(1)|endometrium(2)|kidney(3)|large_intestine(8)|lung(11)|ovary(3)|prostate(1)|skin(2)|urinary_tract(1)	37		Myeloproliferative disorder(115;0.00878)			Irinotecan(DB00762)|Lucanthone(DB04967)|Topotecan(DB01030)	CATTAAAGAGACCTCGAGATG	0.318000			T	NUP98	AML*									164			4		0	0	1	0	0
C1orf129	80133	broad.mit.edu	37	1	170993854	170993854	+	Missense_Mutation	SNP	A	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr1:170993854A>T	uc010plz.2	+	18	2280	c.2126A>T	c.(2125-2127)aAa>aTa	p.K709I		NM_001163629	NP_001157101	Q5TGP6	CA129_HUMAN	Homo sapiens chromosome 1 open reading frame 129 (C1orf129), transcript variant 1, mRNA.	0							binding			breast(2)|central_nervous_system(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(12)|lung(16)|pancreas(1)|prostate(1)|skin(3)	45	all_hematologic(923;0.0922)|Acute lymphoblastic leukemia(37;0.181)					CGTTTGCTCAAAGATGAAAAT	0.353000														74			7		0	0	1	0	0
SKIV2L2	23517	broad.mit.edu	37	5	54654428	54654428	+	Missense_Mutation	SNP	T	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr5:54654428T>C	uc003jpy.4	+	14	1827	c.1561T>C	c.(1561-1563)Tct>Cct	p.S521P	SKIV2L2_uc011cqi.2_Missense_Mutation_p.S420P	NM_015360	NP_056175	P42285	SK2L2_HUMAN	Homo sapiens superkiller viralicidic activity 2-like 2 (S. cerevisiae) (SKIV2L2), mRNA.	521	Helicase C-terminal.				maturation of 5.8S rRNA	catalytic step 2 spliceosome|nucleolus	ATP binding|ATP-dependent helicase activity|nucleic acid binding|protein binding			NS(2)|endometrium(7)|haematopoietic_and_lymphoid_tissue(2)|kidney(4)|large_intestine(5)|lung(12)|ovary(1)|prostate(4)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	41		Lung NSC(810;0.000744)|Breast(144;0.181)|Prostate(74;0.194)				CATTCAGATGTCTGGTCGTGC	0.323000														70			4		0	0	1	0	0
ITGA8	8516	broad.mit.edu	37	10	15719635	15719635	+	Splice_Site	SNP	T	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr10:15719635T>C	uc001ioc.1	-	6	631	c.631_splice	c.e6-1	p.N211_splice	ITGA8_uc010qcb.1_Splice_Site_p.N211_splice	NM_003638	NP_003629	P53708	ITA8_HUMAN	Homo sapiens integrin, alpha 8 (ITGA8), mRNA.	211					cell differentiation|cell-cell adhesion|cell-matrix adhesion|integrin-mediated signaling pathway|nervous system development	integrin complex	receptor activity			NS(2)|breast(1)|cervix(1)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(10)|lung(57)|ovary(3)|prostate(1)|skin(2)|stomach(1)|upper_aerodigestive_tract(4)|urinary_tract(3)	96						AAGGTCTCCATTCTACAAAAC	0.368000														28			3		0	0	1	0	0
ALDH1A3	220	broad.mit.edu	37	15	101427815	101427815	+	Silent	SNP	C	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr15:101427815C>A	uc002bwn.4	+	2	347	c.243C>A	c.(241-243)gcC>gcA	p.A81A	ALDH1A3_uc010bpb.3_Silent_p.A81A	NM_000693	NP_000684	P47895	AL1A3_HUMAN	Homo sapiens aldehyde dehydrogenase 1 family, member A3 (ALDH1A3), mRNA.	81					retinal metabolic process	cytoplasm	aldehyde dehydrogenase|protein homodimerization activity			NS(1)|central_nervous_system(2)|endometrium(3)|large_intestine(7)|lung(9)|pancreas(1)|prostate(2)|skin(1)|urinary_tract(1)	27	Lung NSC(78;0.00144)|all_lung(78;0.0018)|Melanoma(26;0.00852)		OV - Ovarian serous cystadenocarcinoma(32;0.000932)|LUSC - Lung squamous cell carcinoma(107;0.0766)|Lung(145;0.103)		NADH(DB00157)|Vitamin A(DB00162)	CACAGGTTGCCTTCCAGAGGG	0.637000														55			46		1.77791e-30	1.8235e-30	1	1	0
ZNF561	93134	broad.mit.edu	37	19	9724753	9724753	+	Missense_Mutation	SNP	G	A	A	rs144117005	by1000genomes	TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr19:9724753G>A	uc002mlu.3	-	4	473	c.268C>T	c.(268-270)Cgg>Tgg	p.R90W	ZNF561_uc010dwu.3_Missense_Mutation_p.R21W|ZNF561_uc010xkr.2_Intron	NM_152289	NP_689502	Q8N587	ZN561_HUMAN	Homo sapiens zinc finger protein 561 (ZNF561), mRNA.	90	KRAB.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding	p.H90Q(1)		breast(2)|endometrium(1)|kidney(2)|large_intestine(3)|lung(5)|ovary(1)	14						AGTGATGACCGTTTGGTTCTA	0.313000														182			4		0	0	1	0	0
NRP2	8828	broad.mit.edu	37	2	206605324	206605324	+	Missense_Mutation	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr2:206605324C>T	uc002vaw.3	+	7	2019	c.1228C>T	c.(1228-1230)Cgc>Tgc	p.R410C	NRP2_uc002vat.3_Missense_Mutation_p.R410C|NRP2_uc002vau.3_Missense_Mutation_p.R410C|NRP2_uc002vav.3_Missense_Mutation_p.R410C|NRP2_uc002vax.3_Missense_Mutation_p.R410C|NRP2_uc002vay.3_Missense_Mutation_p.R410C|NRP2_uc010fud.3_Missense_Mutation_p.R410C	NM_201266	NP_957718	O60462	NRP2_HUMAN	Homo sapiens neuropilin 2 (NRP2), transcript variant 1, mRNA.	410	F5/8 type C 1.				angiogenesis|axon guidance|cell adhesion	integral to membrane|membrane fraction|plasma membrane	heparin binding|metal ion binding|semaphorin receptor activity|vascular endothelial growth factor receptor activity	p.R410C(2)		NS(1)|breast(1)|central_nervous_system(1)|endometrium(4)|kidney(2)|large_intestine(14)|lung(19)|ovary(1)|pancreas(1)|prostate(4)|skin(2)|upper_aerodigestive_tract(2)	52						TGTTAGAATCCGCCCTCAGAC	0.557000														41			4		0	0	1	0	0
ZNF560	147741	broad.mit.edu	37	19	9578613	9578613	+	Missense_Mutation	SNP	A	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr19:9578613A>T	uc002mlp.1	-	9	1220	c.1010T>A	c.(1009-1011)gTa>gAa	p.V337E	ZNF560_uc010dwr.1_Missense_Mutation_p.V231E	NM_152476	NP_689689	Q96MR9	ZN560_HUMAN	Homo sapiens zinc finger protein 560 (ZNF560), mRNA.	337					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding	p.V337A(2)|p.V337L(1)		NS(1)|breast(3)|endometrium(3)|kidney(2)|large_intestine(16)|liver(2)|lung(24)|ovary(2)|pancreas(1)|prostate(1)|skin(5)|stomach(1)|upper_aerodigestive_tract(4)	65						TTCAACATTTACAGCATGGCT	0.393000														234			24		0	0	1	0	0
HERC2P2	400322	broad.mit.edu	37	15	23285556	23285556	+	RNA	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr15:23285556G>A	uc001yvq.2	-	10		c.2359C>T			HERC2P2_uc001yvo.4_Intron|HERC2P2_uc001yvp.4_Intron					Homo sapiens hect domain and RLD 2 pseudogene 2 (HERC2P2), non-coding RNA.																		CCACCCCGGCGTGATTGTGAC	0.498000														10			12		0	0	1	0	0
STON2	85439	broad.mit.edu	37	14	81737175	81737175	+	Missense_Mutation	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr14:81737175C>T	uc010tvu.2	-	4	2650	c.2452G>A	c.(2452-2454)Ggc>Agc	p.G818S	STON2_uc001xvk.1_Missense_Mutation_p.G818S|STON2_uc010tvt.2_Missense_Mutation_p.G615S	NM_033104	NP_149095	Q8WXE9	STON2_HUMAN	Homo sapiens stonin 2 (STON2), transcript variant 1, mRNA.	818	MHD.				endocytosis|intracellular protein transport|regulation of endocytosis	clathrin adaptor complex|nucleolus	protein binding			breast(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(7)|lung(13)|pancreas(2)|prostate(1)|skin(5)	34				BRCA - Breast invasive adenocarcinoma(234;0.0348)		CGGTCAGAGCCGAGTTCAAGG	0.498000														88			3		0	0	1	0	0
INVS	27130	broad.mit.edu	37	9	103004868	103004868	+	Silent	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr9:103004868C>T	uc004bap.1	+	6	1025	c.813C>T	c.(811-813)gtC>gtT	p.V271V	INVS_uc010mta.2_Silent_p.V175V|INVS_uc011lve.1_Silent_p.V175V|INVS_uc004bao.1_Silent_p.V271V|INVS_uc004baq.1_Silent_p.V175V|INVS_uc004bar.1_Silent_p.V175V|INVS_uc010mtb.1_5'UTR	NM_014425	NP_055240	Q9Y283	INVS_HUMAN	Homo sapiens inversin (INVS), transcript variant 1, mRNA.	271					Wnt receptor signaling pathway|negative regulation of canonical Wnt receptor signaling pathway	cytoplasm|membrane|microtubule|nucleus|spindle	calmodulin binding			breast(2)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(7)|lung(5)|ovary(4)|prostate(1)|skin(2)|stomach(1)|upper_aerodigestive_tract(1)	31		Acute lymphoblastic leukemia(62;0.056)				CACAGATTGTCCATCTCCTTT	0.343000														9			64		0	0	1	0	0
ETV5	2119	broad.mit.edu	37	3	185783822	185783822	+	Silent	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr3:185783822A>G	uc003fpy.3	-	7	881	c.816T>C	c.(814-816)ccT>ccC	p.P272P	ETV5_uc003fpz.3_Silent_p.P230P	NM_004454	NP_004445	P41161	ETV5_HUMAN	Homo sapiens ets variant 5 (ETV5), mRNA.	230					cellular response to oxidative stress	nucleus	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity|transcription regulatory region DNA binding			breast(2)|cervix(1)|large_intestine(7)|lung(9)|ovary(2)|prostate(1)|skin(4)|upper_aerodigestive_tract(2)	28	all_cancers(143;4.06e-12)|Ovarian(172;0.0386)|Breast(254;0.247)		OV - Ovarian serous cystadenocarcinoma(80;1.62e-24)			CTGGCTGAGGAGGGAAGGGGT	0.488000			T	"""TMPRSS2, SCL45A3"""	Prostate									106			4		0	0	1	0	0
TTLL6	284076	broad.mit.edu	37	17	46882179	46882179	+	Missense_Mutation	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr17:46882179A>G	uc021tzm.1	-	1	313	c.278T>C	c.(277-279)cTt>cCt	p.L93P	TTLL6_uc002ioc.3_5'UTR|TTLL6_uc002iod.3_5'UTR	NM_001130918	NP_001124390	Q8N841	TTLL6_HUMAN	Homo sapiens tubulin tyrosine ligase-like family, member 6 (TTLL6), transcript variant 1, mRNA.	45	TTL.					cilium|microtubule basal body	ATP binding|tubulin binding|tubulin-tyrosine ligase activity			endometrium(1)|large_intestine(5)|lung(9)|prostate(1)|skin(2)	18						GGCATTCTGAAGTCCGTTTTG	0.498000											OREG0024527	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)		53			4		0	0	1	0	0
PLEKHH1	57475	broad.mit.edu	37	14	68052685	68052685	+	Nonsense_Mutation	SNP	C	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr14:68052685C>A	uc001xjl.1	+	27	3946	c.3804C>A	c.(3802-3804)taC>taA	p.Y1268*	PLEKHH1_uc010tsw.1_Nonsense_Mutation_p.Y836*|PLEKHH1_uc001xjn.1_Nonsense_Mutation_p.Y783*|PLEKHH1_uc010tsx.1_Nonsense_Mutation_p.Y133*|PLEKHH1_uc001xjo.1_Nonsense_Mutation_p.Y133*|PLEKHH1_uc001xjp.1_Nonsense_Mutation_p.Y133*	NM_020715	NP_065766	Q9ULM0	PKHH1_HUMAN	Homo sapiens pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 (PLEKHH1), mRNA.	1268	FERM.					cytoskeleton	binding			endometrium(2)|kidney(4)|lung(12)|urinary_tract(1)	19				all cancers(60;0.000771)|OV - Ovarian serous cystadenocarcinoma(108;0.00502)|BRCA - Breast invasive adenocarcinoma(234;0.011)		ACATCACTTACCCCTACTCTT	0.498000														69			60		5.80444e-35	6.10993e-35	1	1	0
GALK2	2585	broad.mit.edu	37	15	49493438	49493438	+	Missense_Mutation	SNP	A	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr15:49493438A>G	uc001zxj.1	+	1	231	c.133A>G	c.(133-135)Aac>Gac	p.N45D	GALK2_uc001zxi.1_Missense_Mutation_p.N34D|GALK2_uc010ufb.1_Missense_Mutation_p.N21D|GALK2_uc001zxk.2_Non-coding_Transcript|GALK2_uc010ufc.1_Missense_Mutation_p.N21D|Metazoa_SRP_uc021sku.1_5'Flank	NM_002044	NP_002035	Q01415	GALK2_HUMAN	Homo sapiens galactokinase 2 (GALK2), transcript variant 1, mRNA.	45					galactose metabolic process	cytoplasm	ATP binding|N-acetylgalactosamine kinase activity|galactokinase activity			breast(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(3)|liver(2)|lung(7)|skin(1)|upper_aerodigestive_tract(1)	19		all_lung(180;0.000325)		all cancers(107;3.71e-08)|GBM - Glioblastoma multiforme(94;7e-05)		AGGAAGAGTCAACATAATAGG	0.284000														34			3		0	0	1	0	0
ROBO2	6092	broad.mit.edu	37	3	77526693	77526693	+	Nonsense_Mutation	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr3:77526693C>T	uc011bgk.2	+	2	1160	c.517C>T	c.(517-519)Cga>Tga	p.R173*	ROBO2_uc021xat.1_Nonsense_Mutation_p.R189*|ROBO2_uc003dpy.4_Nonsense_Mutation_p.R173*|ROBO2_uc003dpz.3_Nonsense_Mutation_p.R173*|ROBO2_uc011bgj.2_Non-coding_Transcript	NM_002942	NP_002933	Q9HCK4	ROBO2_HUMAN	Homo sapiens roundabout, axon guidance receptor, homolog 2 (Drosophila) (ROBO2), transcript variant 2, mRNA.	173	Ig-like C2-type 2.				apoptosis involved in luteolysis|axon midline choice point recognition|cellular response to hormone stimulus|homophilic cell adhesion|metanephros development|negative regulation of negative chemotaxis|negative regulation of synaptogenesis|olfactory bulb interneuron development|positive regulation of axonogenesis|retinal ganglion cell axon guidance|ureteric bud development	axolemma|cell surface|integral to membrane	axon guidance receptor activity|identical protein binding			NS(1)|biliary_tract(5)|breast(3)|central_nervous_system(1)|cervix(1)|endometrium(6)|haematopoietic_and_lymphoid_tissue(3)|kidney(3)|large_intestine(23)|liver(1)|lung(52)|ovary(2)|pancreas(2)|prostate(5)|skin(8)|upper_aerodigestive_tract(1)	117				Epithelial(33;0.00199)|LUSC - Lung squamous cell carcinoma(21;0.008)|BRCA - Breast invasive adenocarcinoma(55;0.00884)|Lung(72;0.0183)|KIRC - Kidney renal clear cell carcinoma(39;0.0832)|Kidney(39;0.103)		AGACAAAGTTCGAATTGATGA	0.423000														209			10		0	0	1	0	0
PKDREJ	10343	broad.mit.edu	37	22	46657795	46657795	+	Missense_Mutation	SNP	T	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr22:46657795T>A	uc003bhh.3	-	0	1425	c.1425A>T	c.(1423-1425)agA>agT	p.R475S		NM_006071	NP_006062	Q9NTG1	PKDRE_HUMAN	Homo sapiens polycystic kidney disease (polycystin) and REJ homolog (sperm receptor for egg jelly homolog, sea urchin) (PKDREJ), mRNA.	475	REJ.				acrosome reaction|neuropeptide signaling pathway	integral to membrane	calcium ion binding|ion channel activity			NS(2)|breast(7)|central_nervous_system(1)|cervix(3)|endometrium(4)|kidney(5)|large_intestine(21)|lung(16)|ovary(2)|prostate(6)|skin(4)|upper_aerodigestive_tract(2)	73		Ovarian(80;0.00965)|all_neural(38;0.0416)		UCEC - Uterine corpus endometrioid carcinoma (28;0.00459)		ACAAAGAAAATCTATCAGAGA	0.393000														78			7		0	0	1	0	0
PCDH20	64881	broad.mit.edu	37	13	61989199	61989199	+	Silent	SNP	T	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr13:61989199T>G	uc001vid.4	-	0	457	c.93A>C	c.(91-93)ctA>ctC	p.L31L	PCDH20_uc010thj.2_Silent_p.L31L	NM_022843	NP_073754	Q8N6Y1	PCD20_HUMAN	Homo sapiens protocadherin 20 (PCDH20), mRNA.	4					homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			breast(3)|central_nervous_system(2)|endometrium(3)|kidney(4)|large_intestine(14)|liver(1)|lung(23)|ovary(5)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)	58		Breast(118;0.195)|Prostate(109;0.229)		GBM - Glioblastoma multiforme(99;0.000118)		TGGGACGATGTAGACGCCCCA	0.642000														114			5		0	0	1	0	0
MGC70870	403340	broad.mit.edu	37	GL000205.1	118065	118065	+	RNA	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chrGL000205.1:118065G>A	uc002kgk.4	+	0		c.1443G>A								Homo sapiens C-terminal binding protein 2 pseudogene (MGC70870), non-coding RNA.																		AGTTTTGCTCGGGGTCTGTTG	0.572000														66			3		0	0	1	0	0
ACBD4	79777	broad.mit.edu	37	17	43215198	43215198	+	Splice_Site	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr17:43215198G>A	uc002iid.2	+	7	917	c.573_splice	c.e7+1	p.L191_splice	ACBD4_uc010wjj.2_Splice_Site_p.W204_splice|ACBD4_uc002iie.3_Splice_Site_p.W204_splice|ACBD4_uc002iif.3_Splice_Site_p.L191_splice|ACBD4_uc002iic.3_Splice_Site_p.L191_splice|ACBD4_uc010dae.3_Splice_Site_p.W126_splice	NM_001135707	NP_001129179	Q8NC06	ACBD4_HUMAN	Homo sapiens acyl-CoA binding domain containing 4 (ACBD4), transcript variant 5, mRNA.	191							fatty-acyl-CoA binding			kidney(1)|lung(3)|ovary(1)	5						GCCTGAGCTGGTGAGCCCAGT	0.607000														3			54		0	0	1	0	0
MCM2	4171	broad.mit.edu	37	3	127317314	127317314	+	Splice_Site	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr3:127317314C>T	uc003ejp.3	+	1	63	c.6_splice	c.e1+1	p.A2_splice	MCM2_uc011bkm.2_Splice_Site|MCM2_uc010hsl.3_5'Flank	NM_004526	NP_004517	P49736	MCM2_HUMAN	Homo sapiens minichromosome maintenance complex component 2 (MCM2), mRNA.	2	Interaction with MYST2 (By similarity).				DNA strand elongation involved in DNA replication|DNA-dependent DNA replication initiation|G1/S transition of mitotic cell cycle|M/G1 transition of mitotic cell cycle|S phase of mitotic cell cycle|cell cycle checkpoint	MCM complex|chromatin	ATP binding|helicase activity|metal ion binding			ovary(3)|skin(2)|stomach(1)	6						ACTGCTATGGCGGTGAGCGCG	0.692000														56			3		0	0	1	0	0
HYDIN	54768	broad.mit.edu	37	GL000192.1	311344	311344	+	RNA	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chrGL000192.1:311344C>T	uc010yij.1	-	6		c.1025G>A			HYDIN_uc021vdl.1_Non-coding_Transcript	NM_017558		Q4G0P3	HYDIN_HUMAN	Homo sapiens HYDIN, axonemal central pair apparatus protein (HYDIN), transcript variant 2, mRNA.											breast(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(17)|lung(12)|ovary(2)|skin(3)|stomach(2)|upper_aerodigestive_tract(1)	43		Ovarian(137;0.0654)				TACCTTGCTGCAATTAAGAGC	0.577000														17			3		0	0	1	0	0
MCF2L2	23101	broad.mit.edu	37	3	183028733	183028733	+	Silent	SNP	T	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr3:183028733T>C	uc003fli.1	-	8	1053	c.963A>G	c.(961-963)caA>caG	p.Q321Q	MCF2L2_uc003flj.1_Silent_p.Q321Q|MCF2L2_uc003flp.1_Silent_p.Q356Q|MCF2L2_uc011bqs.1_Non-coding_Transcript	NM_015078	NP_055893	Q86YR7	MF2L2_HUMAN	Homo sapiens MCF.2 cell line derived transforming sequence-like 2 (MCF2L2), mRNA.	321					regulation of Rho protein signal transduction	intracellular	Rho guanyl-nucleotide exchange factor activity			breast(2)|endometrium(5)|kidney(4)|large_intestine(22)|lung(25)|ovary(3)|prostate(4)|skin(4)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	72	all_cancers(143;1.26e-12)|Ovarian(172;0.0355)		all cancers(12;3.35e-44)|Epithelial(37;6.48e-38)|LUSC - Lung squamous cell carcinoma(7;7.12e-25)|Lung(8;6.39e-23)|OV - Ovarian serous cystadenocarcinoma(80;6.75e-21)			AATGCTGTAGTTGTAGGCACT	0.393000														113			4		0	0	1	0	0
HAS3	3038	broad.mit.edu	37	16	69148916	69148916	+	Missense_Mutation	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr16:69148916G>A	uc010cfh.3	+	3	1633	c.1409G>A	c.(1408-1410)gGc>gAc	p.G470D	HAS3_uc002ewk.3_Intron|HAS3_uc002ewl.3_Missense_Mutation_p.G470D	NM_001199280	NP_001186209	O00219	HAS3_HUMAN	Homo sapiens hyaluronan synthase 3 (HAS3), transcript variant 3, mRNA.	470					carbohydrate metabolic process	integral to plasma membrane	hyaluronan synthase activity			cervix(1)|endometrium(2)|kidney(2)|large_intestine(4)|lung(5)|urinary_tract(2)	16		Ovarian(137;0.101)		OV - Ovarian serous cystadenocarcinoma(108;0.0694)		GGCACCTCTGGCCGAAAAACC	0.532000														74			74		0	0	1	0	0
APOBEC1	339	broad.mit.edu	37	12	7802197	7802197	+	Silent	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr12:7802197C>T	uc001qtb.3	-	4	691	c.657G>A	c.(655-657)ccG>ccA	p.P219P	APOBEC1_uc001qtc.3_Silent_p.P174P	NM_001644	NP_001635	P41238	ABEC1_HUMAN	Homo sapiens apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 (APOBEC1), mRNA.	219					DNA demethylation|cytidine to uridine editing|lipid metabolic process|mRNA modification|mRNA processing|negative regulation of methylation-dependent chromatin silencing	nucleoplasm	RNA binding|cytidine deaminase activity|zinc ion binding			kidney(2)|large_intestine(2)|lung(10)|prostate(1)|skin(1)|stomach(1)	17						GGATGTGTGGCGGAATCGTTT	0.408000														140			6		0	0	1	0	0
DGCR6L	85359	broad.mit.edu	37	22	20302561	20302561	+	Missense_Mutation	SNP	C	T	T	rs141884869	by1000genomes	TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr22:20302561C>T	uc010gsc.3	-	3	928	c.811G>A	c.(811-813)Ggc>Agc	p.G271S	DGCR6L_uc002zrx.3_Intron|DGCR6L_uc010gsb.3_Intron			Q9BY27	DGC6L_HUMAN	Homo sapiens DiGeorge syndrome critical region gene 6-like (DGCR6L), mRNA.	0						nucleus				endometrium(1)|kidney(1)|lung(2)|stomach(1)	5	Colorectal(54;0.0993)					GAATCTGAGCCTCTGCCCCCA	0.667000														32			4		0	0	1	0	0
NKX3-1	4824	broad.mit.edu	37	8	23538897	23538897	+	Missense_Mutation	SNP	C	T	T	rs150251660		TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr8:23538897C>T	uc011kzx.2	-	1	590	c.542G>A	c.(541-543)cGa>cAa	p.R181Q	NKX3-1_uc003xdv.1_Intron	NM_006167	NP_006158	Q99801	NKX31_HUMAN	Homo sapiens NK3 homeobox 1 (NKX3-1), transcript variant 1, mRNA.	181					negative regulation of estrogen receptor binding|negative regulation of transcription, DNA-dependent|positive regulation of cell division|positive regulation of mitotic cell cycle|positive regulation of transcription from RNA polymerase II promoter	nucleus	estrogen receptor activity|estrogen receptor binding|sequence-specific DNA binding transcription factor activity|transcription regulatory region sequence-specific DNA binding			large_intestine(3)|lung(4)|prostate(5)|skin(2)	14		Prostate(55;0.114)		Colorectal(74;0.0146)|COAD - Colon adenocarcinoma(73;0.061)|BRCA - Breast invasive adenocarcinoma(99;0.0708)		GAGCTGCTTTCGCTTAGTCTT	0.582000														93			3		0	0	1	0	0
MYT1	4661	broad.mit.edu	37	20	62839675	62839675	+	Missense_Mutation	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr20:62839675G>A	uc002yii.3	+	6	1490	c.1126G>A	c.(1126-1128)Gga>Aga	p.G376R	MYT1_uc002yih.3_Intron|MYT1_uc002yij.3_Missense_Mutation_p.G8R	NM_004535	NP_004526	Q01538	MYT1_HUMAN	Homo sapiens myelin transcription factor 1 (MYT1), mRNA.	376					cell differentiation|nervous system development	nucleus	DNA binding|protein binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			breast(4)|central_nervous_system(1)|cervix(1)|endometrium(4)|kidney(3)|large_intestine(12)|liver(1)|lung(17)|ovary(5)|prostate(2)|skin(2)|soft_tissue(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	55	all_cancers(38;1.82e-11)|all_epithelial(29;3.3e-13)|Lung NSC(23;5.21e-10)|all_lung(23;1.92e-09)					GATGACCCGGGGAAACCTGGG	0.637000														89			11		0	0	1	0	0
CNDP1	84735	broad.mit.edu	37	18	72238436	72238436	+	Missense_Mutation	SNP	C	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr18:72238436C>A	uc002llq.3	+	6	983	c.772C>A	c.(772-774)Cag>Aag	p.Q258K	CNDP1_uc002lls.3_Missense_Mutation_p.Q61K	NM_032649	NP_116038	Q96KN2	CNDP1_HUMAN	Homo sapiens carnosine dipeptidase 1 (metallopeptidase M20 family) (CNDP1), mRNA.	258					proteolysis	extracellular region	carboxypeptidase activity|dipeptidase activity|metal ion binding|metallopeptidase activity|tripeptidase activity			breast(1)|central_nervous_system(1)|endometrium(2)|kidney(3)|large_intestine(4)|lung(12)|prostate(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)	27		Esophageal squamous(42;0.129)|Prostate(75;0.157)|Melanoma(33;0.211)		BRCA - Breast invasive adenocarcinoma(31;0.109)		ATGCAGAGACCAGGATTTTCA	0.408000														128			110		2.2287e-75	2.40941e-75	1	1	0
SERPINB12	89777	broad.mit.edu	37	18	61223519	61223519	+	Missense_Mutation	SNP	C	T	T			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr18:61223519C>T	uc010xeo.2	+	0	127	c.127C>T	c.(127-129)Cgc>Tgc	p.R43C	SERPINB12_uc010xen.2_Missense_Mutation_p.R43C	NM_080474	NP_536722	Q96P63	SPB12_HUMAN	Homo sapiens serpin peptidase inhibitor, clade B (ovalbumin), member 12 (SERPINB12), mRNA.	43					negative regulation of protein catabolic process|regulation of proteolysis	cytoplasm	enzyme binding|serine-type endopeptidase inhibitor activity			kidney(1)|large_intestine(5)|lung(19)|skin(1)	26						TGGTATGGTACGCTTGGGTGC	0.453000														78			92		0	0	1	0	0
CD52	1043	broad.mit.edu	37	1	26644516	26644516	+	Missense_Mutation	SNP	G	A	A			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr1:26644516G>A	uc001bmc.3	+	0	106	c.8G>A	c.(7-9)cGc>cAc	p.R3H	UBXN11_uc001bma.3_Intron|CD52_uc009vsg.1_Non-coding_Transcript	NM_001803	NP_001794	P31358	CD52_HUMAN	Homo sapiens CD52 molecule (CD52), mRNA.	3					elevation of cytosolic calcium ion concentration|respiratory burst	anchored to membrane|integral to plasma membrane|membrane fraction				large_intestine(1)	1		all_cancers(24;5.02e-24)|Colorectal(325;3.46e-05)|all_lung(284;5.94e-05)|Lung NSC(340;7.26e-05)|Renal(390;0.0007)|Ovarian(437;0.00473)|Breast(348;0.00637)|Myeloproliferative disorder(586;0.0255)|all_neural(195;0.0381)		UCEC - Uterine corpus endometrioid carcinoma (279;0.0178)|OV - Ovarian serous cystadenocarcinoma(117;7.56e-28)|Colorectal(126;1.24e-08)|COAD - Colon adenocarcinoma(152;9.31e-07)|KIRC - Kidney renal clear cell carcinoma(1967;0.000716)|BRCA - Breast invasive adenocarcinoma(304;0.000946)|STAD - Stomach adenocarcinoma(196;0.00151)|GBM - Glioblastoma multiforme(114;0.0137)|READ - Rectum adenocarcinoma(331;0.0649)	Alemtuzumab(DB00087)	AAAATGAAGCGCTTCCTCTTC	0.517000														49			4		0	0	1	0	0
FAM184A	79632	broad.mit.edu	37	6	119399412	119399413	+	Frame_Shift_Ins	INS	-	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr6:119399412_119399413insC	uc003pyj.3	-	0	400_401	c.52_53insG	c.(52-54)gccfs	p.A18fs	FAM184A_uc003pyk.4_Intron|FAM184A_uc003pyl.4_Intron	NM_024581	NP_078857	Q8NB25	F184A_HUMAN	Homo sapiens family with sequence similarity 184, member A (FAM184A), transcript variant 1, mRNA.	18										breast(2)|central_nervous_system(2)|endometrium(2)|kidney(5)|large_intestine(19)|lung(13)|ovary(2)|pancreas(1)|prostate(1)|skin(5)	52						CGCGAATTTGGCCGCCGAGCCG	0.658													---	4	---	---	2	---					
UBQLN1	29979	broad.mit.edu	37	9	86322497	86322498	+	Frame_Shift_Ins	INS	-	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr9:86322497_86322498insC	uc004amv.3	-	0	671_672	c.97_98insG	c.(97-99)gagfs	p.E33fs	UBQLN1_uc004amw.3_Frame_Shift_Ins_p.E33fs|AK300656_uc004amx.3_5'Flank	NM_013438	NP_038466	Q9UMX0	UBQL1_HUMAN	Homo sapiens ubiquilin 1 (UBQLN1), transcript variant 1, mRNA.	33					apoptosis|regulation of protein ubiquitination|response to hypoxia	endoplasmic reticulum|nucleus|perinuclear region of cytoplasm|proteasome complex	kinase binding			breast(4)|endometrium(2)|kidney(4)|large_intestine(6)|lung(10)|prostate(1)	27						GATTTTGGGCTCCGCGGAGGCA	0.673													---	8	---	---	4	---					
UBQLN1	29979	broad.mit.edu	37	9	86322500	86322500	+	Frame_Shift_Del	DEL	G	-	-			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr9:86322500delG	uc004amv.3	-	0	669	c.95delC	c.(94-96)gcgfs	p.A32fs	UBQLN1_uc004amw.3_Frame_Shift_Del_p.A32fs|AK300656_uc004amx.3_5'Flank	NM_013438	NP_038466	Q9UMX0	UBQL1_HUMAN	Homo sapiens ubiquilin 1 (UBQLN1), transcript variant 1, mRNA.	32					apoptosis|regulation of protein ubiquitination|response to hypoxia	endoplasmic reticulum|nucleus|perinuclear region of cytoplasm|proteasome complex	kinase binding			breast(4)|endometrium(2)|kidney(4)|large_intestine(6)|lung(10)|prostate(1)	27						TTTGGGCTCCGCGGAGGCAGC	0.672													---	4	---	---	5	---					
UBQLN1	29979	broad.mit.edu	37	9	86322502	86322505	+	Frame_Shift_Del	DEL	GGAG	-	-			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr9:86322502_86322505delGGAG	uc004amv.3	-	0	664_667	c.90_93delCTCC	c.(88-93)gcctccfs	p.A30fs	UBQLN1_uc004amw.3_Frame_Shift_Del_p.A30fs|AK300656_uc004amx.3_5'Flank	NM_013438	NP_038466	Q9UMX0	UBQL1_HUMAN	Homo sapiens ubiquilin 1 (UBQLN1), transcript variant 1, mRNA.	30					apoptosis|regulation of protein ubiquitination|response to hypoxia	endoplasmic reticulum|nucleus|perinuclear region of cytoplasm|proteasome complex	kinase binding			breast(4)|endometrium(2)|kidney(4)|large_intestine(6)|lung(10)|prostate(1)	27						TGGGCTCCGCGGAGGCAGCGGCCG	0.676													---	3	---	---	5	---					
OR5M1	390168	broad.mit.edu	37	11	56380362	56380363	+	Frame_Shift_Del	DEL	TT	-	-			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr11:56380362_56380363delTT	uc001nja.1	-	0	616_617	c.616_617delAA	c.(616-618)aatfs	p.N206fs	OR8U8_uc001nit.2_Intron	NM_001004740	NP_001004740	Q8NGP8	OR5M1_HUMAN	Homo sapiens olfactory receptor, family 5, subfamily M, member 1 (OR5M1), mRNA.	206					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			central_nervous_system(2)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|lung(7)|upper_aerodigestive_tract(1)	12						GCTTGAGAGATTAAAGCCTGCA	0.441													---	302	---	---	11	---					
PRH2	5555	broad.mit.edu	37	12	11083460	11083461	+	Frame_Shift_Ins	INS	-	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr12:11083460_11083461insC	uc009zhr.3	+	2	339_340	c.300_301insC	c.(298-303)catcccfs	p.H100fs	PRH1_uc001qzb.4_Intron|TAS2R14_uc021qve.1_Intron|PRH1_uc021qvg.1_Intron|PRB4_uc001qzf.1_Intron|PRH2_uc001qzh.3_Intron|PRH2_uc001qzi.4_Frame_Shift_Ins_p.H100fs	NM_001110213	NP_005033	P02810	PRPC_HUMAN	Homo sapiens proline-rich protein HaeIII subfamily 2 (PRH2), transcript variant 2, mRNA.	100						extracellular space	protein binding			breast(1)|endometrium(5)|kidney(2)|large_intestine(1)|lung(3)|upper_aerodigestive_tract(1)	13						AGGGAGGCCATCCCCCTCCTCC	0.644													---	178	---	---	7	---					
CLN3	1201	broad.mit.edu	37	16	28503050	28503051	+	Frame_Shift_Ins	INS	-	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr16:28503050_28503051insC	uc002dpo.3	-	0	353_354	c.30_31insG	c.(28-33)cgctttfs	p.R10fs	NPIPL1_uc010vct.2_Intron|CLN3_uc002dpl.3_5'UTR|CLN3_uc002dpm.3_5'UTR|CLN3_uc010vcu.2_5'UTR|CLN3_uc010vcv.2_Frame_Shift_Ins_p.R10fs|CLN3_uc002dpp.3_Frame_Shift_Ins_p.R10fs|CLN3_uc021tfs.1_5'Flank|CLN3_uc002dpt.1_5'UTR|CLN3_uc002dpq.1_Frame_Shift_Ins_p.R10fs|CLN3_uc010bye.1_Frame_Shift_Ins_p.R10fs|CLN3_uc002dpr.1_Non-coding_Transcript|CLN3_uc010byf.1_Non-coding_Transcript|CLN3_uc002dps.1_Frame_Shift_Ins_p.A12fs|CLN3_uc002dpu.1_5'UTR|CLN3_uc002dpw.1_5'UTR|CLN3_uc010vcw.1_5'UTR|CLN3_uc002dqa.2_Frame_Shift_Ins_p.R10fs|CLN3_uc010vcx.1_5'UTR|CLN3_uc002dpx.1_Frame_Shift_Ins_p.R10fs|CLN3_uc002dpy.1_Frame_Shift_Ins_p.A12fs|CLN3_uc002dpz.1_Non-coding_Transcript|APOBR_uc002dqb.2_5'Flank|APOBR_uc010byg.2_5'Flank	NM_000086	NP_001035897	Q13286	CLN3_HUMAN	Homo sapiens ceroid-lipofuscinosis, neuronal 3 (CLN3), transcript variant 2, mRNA.	10					amyloid precursor protein catabolic process|arginine transport|associative learning|autophagic vacuole fusion|cell death|cellular amino acid metabolic process|cytosolic calcium ion homeostasis|galactosylceramide metabolic process|globoside metabolic process|glucosylceramide metabolic process|ionotropic glutamate receptor signaling pathway|lysosomal lumen acidification|lysosomal lumen pH elevation|negative regulation of catalytic activity|negative regulation of macroautophagy|negative regulation of neuron apoptosis|negative regulation of proteolysis|neuromuscular process controlling balance|neurotransmitter metabolic process|protein catabolic process|protein folding|protein processing|receptor-mediated endocytosis|regulation of action potential|sphingomyelin metabolic process|vacuolar transport	Golgi membrane|Golgi stack|autophagic vacuole|caveola|cytosol|early endosome|integral to endoplasmic reticulum membrane|late endosome|lysosomal membrane|membrane fraction|mitochondrion|neuron projection|nucleus|synaptic vesicle|trans-Golgi network	unfolded protein binding			breast(1)|large_intestine(2)|lung(11)|upper_aerodigestive_tract(1)	15						GAATCCGAAAAGCGCCGCCGCG	0.653											OREG0023706	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)	---	41	---	---	7	---					
LHX1	3975	broad.mit.edu	37	17	35297586	35297587	+	Splice_Site	INS	-	C	C			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr17:35297586_35297587insC	uc002hnh.2	+	2	894	c.171_splice	c.e2-1	p.R57_splice	LHX1_uc010cux.1_Splice_Site	NM_005568	NP_005559	P48742	LHX1_HUMAN	Homo sapiens LIM homeobox 1 (LHX1), mRNA.	57					S-shaped body morphogenesis|cerebellar Purkinje cell differentiation|cerebellar Purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation|cervix development|comma-shaped body morphogenesis|dorsal/ventral pattern formation|ectoderm formation|embryonic pattern specification|embryonic retina morphogenesis in camera-type eye|embryonic viscerocranium morphogenesis|endoderm formation|forebrain regionalization|head development|motor axon guidance|negative regulation of transcription, DNA-dependent|nephric duct morphogenesis|nephron tubule epithelial cell differentiation|neuron migration|oviduct epithelium development|paramesonephric duct development|positive regulation of anterior head development|positive regulation of branching involved in ureteric bud morphogenesis|positive regulation of embryonic development|positive regulation of gastrulation|positive regulation of transcription, DNA-dependent|post-embryonic development|primitive streak formation|renal vesicle morphogenesis|retina layer formation|spinal cord association neuron differentiation|transcription from RNA polymerase II promoter|ureteric bud development|uterine epithelium development|vagina development	nucleus|protein complex	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity|transcription corepressor activity|zinc ion binding			NS(1)|central_nervous_system(1)|endometrium(3)|kidney(2)|large_intestine(1)|lung(5)|ovary(1)|prostate(1)|skin(1)	16		Breast(25;0.00607)				cccccCCGCAGGTGTTTCGGTA	0.644													---	4	---	---	2	---					
MUC16	94025	broad.mit.edu	37	19	9054266	9054267	+	Frame_Shift_Ins	INS	-	G	G			TCGA-KL-8325-01A-11D-2310-10	TCGA-KL-8325-11A-01D-2310-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	9fc0e0e8-1b0f-400c-b4cf-126193283695	4ff5a4a6-94f8-4f4c-ae7c-9b1ddb971fb7	g.chr19:9054266_9054267insG	uc002mkp.3	-	3	31559_31560	c.31355_31356insC	c.(31354-31356)cctfs	p.P10452fs		NM_024690	NP_078966	Q8WXI7	MUC16_HUMAN	Homo sapiens mucin 16, cell surface associated (MUC16), mRNA.	10454	Thr-rich.				cell adhesion	extracellular space|extrinsic to membrane|integral to membrane|plasma membrane	protein binding			NS(9)|autonomic_ganglia(1)|breast(26)|central_nervous_system(11)|cervix(1)|endometrium(46)|haematopoietic_and_lymphoid_tissue(5)|kidney(35)|large_intestine(91)|liver(1)|lung(278)|ovary(17)|pancreas(2)|prostate(17)|skin(18)|soft_tissue(1)|stomach(8)|upper_aerodigestive_tract(16)|urinary_tract(7)	590						TGGATGTCTGAGGGCCTTTGAC	0.470													---	251	---	---	9	---					
