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
PEG3	5178	broad.mit.edu	37	19	57327003	57327003	+	Missense_Mutation	SNP	C	T	T	rs140722468		TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr19:57327003C>T	uc002qnu.2	-	6	3158	c.2807G>A	c.(2806-2808)cGt>cAt	p.R936H	PEG3_uc010ygr.1_Intron|PEG3_uc010ygq.1_Intron|PEG3_uc002qnr.2_Intron|PEG3_uc010etp.2_Intron|PEG3_uc010ygs.1_Intron|PEG3_uc002qnq.2_Intron|PEG3_uc002qnt.2_Missense_Mutation_p.R907H|PEG3_uc002qnv.2_Missense_Mutation_p.R936H|PEG3_uc002qnw.2_Missense_Mutation_p.R812H|PEG3_uc002qnx.2_Missense_Mutation_p.R810H|PEG3_uc010etr.2_Missense_Mutation_p.R936H	NM_001146186	NP_001139657	Q9GZU2	PEG3_HUMAN	Homo sapiens paternally expressed 3 (PEG3), transcript variant 4, mRNA.	936					apoptosis|viral reproduction	cytoplasm|nucleus	nucleic acid binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			NS(1)|biliary_tract(4)|breast(2)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(9)|large_intestine(27)|lung(84)|ovary(8)|pancreas(5)|prostate(6)|skin(8)|stomach(2)|upper_aerodigestive_tract(6)	170		Colorectal(82;0.000256)|all_neural(62;0.103)|Ovarian(87;0.243)		GBM - Glioblastoma multiforme(193;0.0269)		CTTTTTAGCACGAGCCTTCTG	0.448000														149			23		0	0	1	0	0
LPIN1	23175	broad.mit.edu	37	2	11907890	11907890	+	Splice_Site	SNP	T	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr2:11907890T>A	uc010yjm.2	+	4	393	c.340_splice	c.e4-1	p.V114_splice	LPIN1_uc010yjn.2_Splice_Site_p.V65_splice|LPIN1_uc002rbt.3_Splice_Site_p.V65_splice|LPIN1_uc002rbs.3_Splice_Site_p.V65_splice	NM_145693	NP_663731	Q14693	LPIN1_HUMAN	Homo sapiens lipin 1 (LPIN1), mRNA.	65					fatty acid catabolic process|transcription, DNA-dependent|triglyceride biosynthetic process|triglyceride mobilization	cytosol|endoplasmic reticulum membrane	phosphatidate phosphatase activity			autonomic_ganglia(1)|breast(1)|cervix(1)|endometrium(2)|kidney(5)|large_intestine(15)|liver(1)|lung(10)|ovary(2)|prostate(2)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(2)	45	all_hematologic(175;0.127)|Acute lymphoblastic leukemia(172;0.155)			Epithelial(75;0.11)|OV - Ovarian serous cystadenocarcinoma(76;0.173)		TCCCTTCAGGTTGACATAGAA	0.423000														117			9		0	0	1	0	0
KIFAP3	22920	broad.mit.edu	37	1	170004687	170004687	+	Silent	SNP	G	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr1:170004687G>A	uc001ggv.3	-	5	796	c.525C>T	c.(523-525)gcC>gcT	p.A175A	KIFAP3_uc021pep.1_Silent_p.A135A|KIFAP3_uc010ply.2_Silent_p.A97A|KIFAP3_uc001ggw.2_Silent_p.A131A	NM_014970	NP_001191446	Q92845	KIFA3_HUMAN	Homo sapiens kinesin-associated protein 3 (KIFAP3), transcript variant 1, mRNA.	175					blood coagulation|plus-end-directed vesicle transport along microtubule|protein complex assembly|signal transduction	centrosome|condensed nuclear chromosome|cytosol|endoplasmic reticulum|kinesin II complex|spindle microtubule	kinesin binding			endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(3)|lung(18)|prostate(2)|skin(3)|urinary_tract(2)	35	all_hematologic(923;0.0922)|Acute lymphoblastic leukemia(37;0.181)					ATGCACCAAGGGCAGTTTCTA	0.368000														60			3		0	0	1	0	0
EVC2	132884	broad.mit.edu	37	4	5564754	5564754	+	Missense_Mutation	SNP	C	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr4:5564754C>T	uc003gij.3	-	21	3802	c.3748G>A	c.(3748-3750)Ggc>Agc	p.G1250S	EVC2_uc003gik.3_Missense_Mutation_p.G1170S|EVC2_uc011bwb.2_Missense_Mutation_p.G690S	NM_147127	NP_667338	Q86UK5	LBN_HUMAN	Homo sapiens Ellis van Creveld syndrome 2 (EVC2), transcript variant 1, mRNA.	1250						integral to membrane				NS(2)|breast(3)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(32)|lung(28)|ovary(4)|pancreas(1)|prostate(2)|skin(2)|stomach(1)|urinary_tract(2)	81						GCCAGTTCGCCAATGGGCTCC	0.443000														100			14		0	0	1	0	0
CSMD2	114784	broad.mit.edu	37	1	34037290	34037290	+	Missense_Mutation	SNP	T	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr1:34037290T>C	uc001bxm.1	-	50	7976	c.7799A>G	c.(7798-7800)gAg>gGg	p.E2600G	CSMD2_uc001bxn.1_Missense_Mutation_p.E2602G	NM_052896	NP_443128	Q7Z408	CSMD2_HUMAN	Homo sapiens CUB and Sushi multiple domains 2 (CSMD2), mRNA.	2602	Sushi 16.					integral to membrane|plasma membrane	protein binding			NS(5)|breast(5)|central_nervous_system(3)|cervix(2)|endometrium(20)|haematopoietic_and_lymphoid_tissue(4)|kidney(9)|large_intestine(43)|lung(114)|ovary(8)|pancreas(1)|prostate(6)|skin(20)|upper_aerodigestive_tract(5)|urinary_tract(1)	246		Myeloproliferative disorder(586;0.0294)|all_neural(195;0.249)				TCGGCCATGCTCCACGCTGAT	0.473000														7			29		0	0	1	0	0
DST	667	broad.mit.edu	37	6	56417323	56417323	+	Nonsense_Mutation	SNP	C	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr6:56417323C>A	uc003pcy.4	-	41	8506	c.8398G>T	c.(8398-8400)Gaa>Taa	p.E2800*		NM_015548	NP_056363	Q03001	DYST_HUMAN	Homo sapiens dystonin (DST), transcript variant 1eA, mRNA.	5212					cell adhesion|cell cycle arrest|cell motility|hemidesmosome assembly|integrin-mediated signaling pathway|intermediate filament cytoskeleton organization|maintenance of cell polarity|microtubule cytoskeleton organization|response to wounding	Z disc|actin cytoskeleton|axon|axon part|basement membrane|cell cortex|cell leading edge|cytoplasmic membrane-bounded vesicle|endoplasmic reticulum membrane|hemidesmosome|integral to membrane|intermediate filament|intermediate filament cytoskeleton|microtubule cytoskeleton|microtubule plus end|nuclear envelope|sarcomere	actin binding|calcium ion binding|integrin binding|microtubule plus-end binding|protein C-terminus binding|protein binding|protein homodimerization activity			NS(1)|breast(5)|central_nervous_system(8)|cervix(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(22)|lung(43)|ovary(7)|prostate(1)|skin(4)|upper_aerodigestive_tract(3)	105	Lung NSC(77;0.103)		LUSC - Lung squamous cell carcinoma(124;0.0485)|Lung(124;0.0956)			TTTATAGTTTCCTTTTGCTTT	0.413000														117			5		8.12818e-05	8.68875e-05	1	1	0
MUC2	4583	broad.mit.edu	37	11	1092624	1092624	+	Silent	SNP	C	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr11:1092624C>A	uc001lsx.1	+	29	4470	c.4443C>A	c.(4441-4443)acC>acA	p.T1481T		NM_002457	NP_002448	Q02817	MUC2_HUMAN	Homo sapiens mucin 2, oligomeric mucus/gel-forming (MUC2), mRNA.	1481	Approximate repeats.					inner mucus layer|outer mucus layer	protein binding			NS(3)|breast(3)|central_nervous_system(1)|cervix(1)|endometrium(26)|haematopoietic_and_lymphoid_tissue(4)|kidney(11)|large_intestine(5)|lung(22)|ovary(2)|prostate(16)|skin(5)|stomach(1)|upper_aerodigestive_tract(2)	102		all_cancers(49;1.08e-07)|all_epithelial(84;5.08e-05)|Breast(177;0.000307)|Ovarian(85;0.000953)|Medulloblastoma(188;0.0109)|all_neural(188;0.0299)|Lung NSC(207;0.191)		BRCA - Breast invasive adenocarcinoma(625;0.000207)|Lung(200;0.0576)|LUSC - Lung squamous cell carcinoma(625;0.0703)	Pranlukast(DB01411)	gccctccaaccaccactccca	0.627000														64			5		1.12685e-05	1.24758e-05	1	1	0
GRM3	2913	broad.mit.edu	37	7	86479693	86479693	+	Missense_Mutation	SNP	C	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr7:86479693C>T	uc003uid.3	+	4	3498	c.2399C>T	c.(2398-2400)aCg>aTg	p.T800M	GRM3_uc010lef.3_Silent_p.D442D|GRM3_uc010leg.3_Missense_Mutation_p.T672M|GRM3_uc010leh.3_Missense_Mutation_p.T392M	NM_000840	NP_000831	Q14832	GRM3_HUMAN	Homo sapiens glutamate receptor, metabotropic 3 (GRM3), mRNA.	800					synaptic transmission	integral to plasma membrane				NS(2)|breast(6)|central_nervous_system(2)|endometrium(4)|haematopoietic_and_lymphoid_tissue(2)|kidney(2)|large_intestine(9)|lung(43)|ovary(3)|pancreas(2)|prostate(4)|skin(25)|upper_aerodigestive_tract(5)	109	Esophageal squamous(14;0.0058)|all_lung(186;0.132)|Lung NSC(181;0.142)				Acamprosate(DB00659)|Nicotine(DB00184)	TAGGTGCAGACGACAACCATG	0.453000														77			26		0	0	1	0	0
CDC25C	995	broad.mit.edu	37	5	137666827	137666827	+	Missense_Mutation	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr5:137666827A>G	uc003lcs.1	-	1	477	c.277T>C	c.(277-279)Tct>Cct	p.S93P	CDC25C_uc003lcp.1_Missense_Mutation_p.S15P|CDC25C_uc003lcq.1_Missense_Mutation_p.S15P|CDC25C_uc003lcr.1_Missense_Mutation_p.S15P|CDC25C_uc011cyp.1_Missense_Mutation_p.S32P|CDC25C_uc010jet.1_Missense_Mutation_p.S15P|CDC25C_uc003lct.1_Missense_Mutation_p.S15P|CDC25C_uc003lcu.1_Missense_Mutation_p.S15P	NM_001790	NP_001781	P30307	MPIP3_HUMAN	Homo sapiens cell division cycle 25 homolog C (S. pombe) (CDC25C), transcript variant 1, mRNA.	15					DNA replication|G2/M transition of mitotic cell cycle|cell cycle checkpoint|cell division|cell proliferation|interspecies interaction between organisms|mitosis|regulation of cyclin-dependent protein kinase activity|regulation of mitosis|traversing start control point of mitotic cell cycle	cytosol|nucleoplasm	WW domain binding|protein tyrosine phosphatase activity	p.L93H(1)		endometrium(2)|kidney(3)|large_intestine(5)|lung(5)|skin(1)	16			KIRC - Kidney renal clear cell carcinoma(527;0.004)|Kidney(363;0.00592)			CCTGAGCCAGAGCTTCCTTCC	0.458000														84			4		0	0	1	0	0
TRAPPC9	83696	broad.mit.edu	37	8	141321473	141321473	+	Splice_Site	SNP	T	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr8:141321473T>C	uc003yvh.2	-	10	1805	c.1790_splice	c.e10-1	p.E597_splice	TRAPPC9_uc003yvj.2_Splice_Site_p.E499_splice|TRAPPC9_uc003yvi.1_Splice_Site_p.E490_splice	NM_031466	NP_001153844	Q96Q05	TPPC9_HUMAN	Homo sapiens trafficking protein particle complex 9 (TRAPPC9), transcript variant 1, mRNA.	499					cell differentiation	Golgi apparatus|endoplasmic reticulum				breast(4)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(7)|liver(1)|lung(16)|ovary(2)|prostate(1)|skin(4)|upper_aerodigestive_tract(3)	47						ATCTTTCTTTTCTGAAGAGAA	0.493000														20			3		0	0	1	0	0
MGC70870	403340	broad.mit.edu	37	GL000205.1	118048	118048	+	RNA	SNP	G	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chrGL000205.1:118048G>C	uc002kgk.4	+	0		c.1426G>C								Homo sapiens C-terminal binding protein 2 pseudogene (MGC70870), non-coding RNA.																		ATGAGTCGGAGCCCTTTAGTT	0.577000														38			6		0	0	1	0	0
SETD1A	9739	broad.mit.edu	37	16	30990508	30990508	+	Missense_Mutation	SNP	C	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr16:30990508C>G	uc002ead.1	+	13	4087	c.3401C>G	c.(3400-3402)cCa>cGa	p.P1134R		NM_014712	NP_055527	O15047	SET1A_HUMAN	Homo sapiens SET domain containing 1A (SETD1A), mRNA.	1134	Pro-rich.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	Set1C/COMPASS complex|chromosome|nuclear speck	RNA binding|histone-lysine N-methyltransferase activity|nucleotide binding|protein binding			NS(2)|breast(2)|central_nervous_system(1)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(9)|lung(21)|ovary(3)|prostate(2)|skin(4)|upper_aerodigestive_tract(4)|urinary_tract(1)	59						CTGCGTCCCCCAGAACCACCT	0.682000														49			6		0	0	1	0	0
RCOR2	283248	broad.mit.edu	37	11	63681937	63681937	+	Missense_Mutation	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr11:63681937A>G	uc001nyc.3	-	5	945	c.557T>C	c.(556-558)aTg>aCg	p.M186T		NM_173587	NP_775858	Q8IZ40	RCOR2_HUMAN	Homo sapiens REST corepressor 2 (RCOR2), mRNA.	186					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding			kidney(2)|large_intestine(3)|liver(1)|lung(5)|ovary(2)|skin(3)|upper_aerodigestive_tract(1)	17						CTGTCTGTCCATCACACTAGT	0.602000														30			6		0	0	1	0	0
HRH1	3269	broad.mit.edu	37	3	11301062	11301062	+	Silent	SNP	G	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr3:11301062G>A	uc010hdr.3	+	1	681	c.339G>A	c.(337-339)gcG>gcA	p.A113A	HRH1_uc010hds.3_Silent_p.A113A|HRH1_uc010hdt.3_Silent_p.A113A|HRH1_uc003bwb.4_Silent_p.A113A|HRH1_uc021wtb.1_Silent_p.A113A	NM_001098213	NP_001091683	P35367	HRH1_HUMAN	Homo sapiens histamine receptor H1 (HRH1), transcript variant 1, mRNA.	113					activation of phospholipase C activity by G-protein coupled receptor protein signaling pathway coupled to IP3 second messenger|inflammatory response	cytoplasm|integral to plasma membrane|nucleus	histamine receptor activity	p.A113A(2)		autonomic_ganglia(1)|central_nervous_system(1)|endometrium(4)|large_intestine(3)|lung(11)|ovary(1)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(2)	25					Aceprometazine(DB01615)|Astemizole(DB00637)|Azatadine(DB00719)|Azelastine(DB00972)|Benzquinamide(DB00767)|Bepotastine(DB04890)|Bromodiphenhydramine(DB01237)|Brompheniramine(DB00835)|Buclizine(DB00354)|Carbinoxamine(DB00748)|Cetirizine(DB00341)|Chlophedianol(DB04837)|Chlorpheniramine(DB01114)|Chlorprothixene(DB01239)|Cinnarizine(DB00568)|Clemastine(DB00283)|Clozapine(DB00363)|Cyclizine(DB01176)|Cyproheptadine(DB00434)|Desipramine(DB01151)|Desloratadine(DB00967)|Dexbrompheniramine(DB00405)|Dimenhydrinate(DB00985)|Diphenhydramine(DB01075)|Diphenylpyraline(DB01146)|Doxepin(DB01142)|Doxylamine(DB00366)|Emedastine(DB01084)|Epinastine(DB00751)|Fexofenadine(DB00950)|Flunarizine(DB04841)|Histamine Phosphate(DB00667)|Hydroxyzine(DB00557)|Ketotifen(DB00920)|Levocabastine(DB01106)|Loratadine(DB00455)|Maprotiline(DB00934)|Meclizine(DB00737)|Mequitazine(DB01071)|Methdilazine(DB00902)|Methotrimeprazine(DB01403)|Mianserin(DB06148)|Mirtazapine(DB00370)|Nedocromil(DB00716)|Olanzapine(DB00334)|Olopatadine(DB00768)|Orphenadrine(DB01173)|Pemirolast(DB00885)|Phenindamine(DB01619)|Pheniramine(DB01620)|Prochlorperazine(DB00433)|Promazine(DB00420)|Promethazine(DB01069)|Propiomazine(DB00777)|Quetiapine(DB01224)|Risperidone(DB00734)|Terfenadine(DB00342)|Thiethylperazine(DB00372)|Trazodone(DB00656)|Trimeprazine(DB01246)|Tripelennamine(DB00792)|Triprolidine(DB00427)|Ziprasidone(DB00246)	CCAGCACAGCGTCCATTTTCA	0.542000														12			20		0	0	1	0	0
MUC4	4585	broad.mit.edu	37	3	195513481	195513481	+	Missense_Mutation	SNP	G	A	A	rs77462830	by1000genomes	TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr3:195513481G>A	uc021xjp.1	-	1	5126	c.4970C>T	c.(4969-4971)gCa>gTa	p.A1657V	MUC4_uc003fvo.3_Intron|MUC4_uc003fvp.3_Intron	NM_018406	NP_060876	Q99102	MUC4_HUMAN	Homo sapiens mucin 4, cell surface associated (MUC4), transcript variant 1, mRNA.	448	VWFD.				cell-matrix adhesion	integral to plasma membrane|proteinaceous extracellular matrix	ErbB-2 class receptor binding|extracellular matrix constituent, lubricant activity			NS(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(3)|kidney(1)|large_intestine(5)|lung(23)|ovary(3)|prostate(8)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	51	all_cancers(143;1.11e-08)|Ovarian(172;0.0634)|Breast(254;0.206)	Lung NSC(153;0.191)	Epithelial(36;3.72e-24)|all cancers(36;6.22e-22)|OV - Ovarian serous cystadenocarcinoma(49;1.1e-18)|Lung(62;4.65e-05)|LUSC - Lung squamous cell carcinoma(58;5.31e-05)	GBM - Glioblastoma multiforme(46;2.37e-05)		ACCTGTGGATGCTGAGGAAGG	0.592000														15			3		0	0	1	0	0
CEP57	9702	broad.mit.edu	37	11	95561021	95561021	+	Silent	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr11:95561021A>G	uc001pfp.2	+	8	1195	c.957A>G	c.(955-957)aaA>aaG	p.K319K	CEP57_uc009ywn.2_Silent_p.K167K|CEP57_uc010ruh.2_Silent_p.K310K|CEP57_uc001pfq.2_Silent_p.K293K|CEP57_uc001pfr.2_Silent_p.K167K	NM_014679	NP_055494	Q86XR8	CEP57_HUMAN	Homo sapiens centrosomal protein 57kDa (CEP57), transcript variant 1, mRNA.	319	Mediates interaction with microtubules (By similarity).				G2/M transition of mitotic cell cycle|fibroblast growth factor receptor signaling pathway|protein import into nucleus, translocation|spermatid development	Golgi apparatus|centrosome|cytosol|microtubule|nucleus	fibroblast growth factor binding|protein homodimerization activity			endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(3)|lung(4)|ovary(1)|prostate(1)	13		Acute lymphoblastic leukemia(157;2.31e-05)|all_hematologic(158;0.00824)				AACACAGTAAAGCTTTGTGCA	0.423000									Mosaic Variegated Aneuploidy Syndrome					122			4		0	0	1	0	0
MYO15A	51168	broad.mit.edu	37	17	18025035	18025035	+	Missense_Mutation	SNP	C	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr17:18025035C>T	uc021trm.1	+	0	3140	c.2921C>T	c.(2920-2922)cCc>cTc	p.P974L	MYO15A_uc021trl.1_Missense_Mutation_p.P974L	NM_016239	NP_057323	Q9UKN7	MYO15_HUMAN	Homo sapiens myosin XVA (MYO15A), mRNA.	974	Myosin head-like.				sensory perception of sound	cytoplasm|myosin complex|stereocilium	ATP binding|actin binding|calmodulin binding|motor activity			breast(5)|central_nervous_system(2)|endometrium(17)|kidney(3)|large_intestine(16)|lung(27)|ovary(3)|pancreas(1)|prostate(6)|skin(13)|stomach(1)|upper_aerodigestive_tract(3)|urinary_tract(2)	99	all_neural(463;0.228)					GTGCCATCCCCCACCCTCCAG	0.657000														87			4		0	0	1	0	0
PTPRN2	5799	broad.mit.edu	37	7	157449123	157449123	+	Missense_Mutation	SNP	G	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr7:157449123G>A	uc003wno.3	-	13	2243	c.2122C>T	c.(2122-2124)Cgc>Tgc	p.R708C	PTPRN2_uc003wnp.3_Missense_Mutation_p.R691C|PTPRN2_uc003wnq.3_Missense_Mutation_p.R679C|PTPRN2_uc003wnr.3_Missense_Mutation_p.R670C|PTPRN2_uc011kwa.2_Missense_Mutation_p.R731C	NM_002847	NP_002838	Q92932	PTPR2_HUMAN	Homo sapiens protein tyrosine phosphatase, receptor type, N polypeptide 2 (PTPRN2), transcript variant 1, mRNA.	708						integral to plasma membrane	protein binding|transmembrane receptor protein tyrosine phosphatase activity			NS(1)|breast(1)|central_nervous_system(1)|cervix(2)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(11)|liver(1)|lung(42)|ovary(4)|pleura(1)|prostate(2)|skin(10)|upper_aerodigestive_tract(1)	86	all_neural(206;0.181)	all_cancers(7;8.99e-13)|all_epithelial(9;2.4e-06)|all_hematologic(28;0.0155)|Breast(660;0.132)	OV - Ovarian serous cystadenocarcinoma(82;0.00463)	STAD - Stomach adenocarcinoma(7;0.0875)		GCGCTGCTGCGTGCGGAGGGG	0.662000														69			4		0	0	1	0	0
ZBBX	79740	broad.mit.edu	37	3	167039952	167039952	+	Silent	SNP	T	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr3:167039952T>C	uc011bpc.2	-	11	1273	c.936A>G	c.(934-936)gaA>gaG	p.E312E	ZBBX_uc003feq.3_Silent_p.E283E|ZBBX_uc003fep.3_Silent_p.E312E	NM_001199201	NP_001186130	A8MT70	ZBBX_HUMAN	Homo sapiens zinc finger, B-box domain containing (ZBBX), transcript variant 1, mRNA.	312						intracellular	zinc ion binding			NS(1)|breast(1)|endometrium(5)|kidney(5)|large_intestine(9)|liver(1)|lung(38)|ovary(2)|prostate(1)|skin(4)|stomach(2)|upper_aerodigestive_tract(1)	70						ATAGAATGTCTTCTTTAAGTT	0.279000														106			4		0	0	1	0	0
SYNDIG1	79953	broad.mit.edu	37	20	24646034	24646034	+	Missense_Mutation	SNP	G	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr20:24646034G>A	uc002wtw.1	+	3	1304	c.671G>A	c.(670-672)cGg>cAg	p.R224Q		NM_024893	NP_079169	Q9H7V2	SYNG1_HUMAN	Homo sapiens synapse differentiation inducing 1 (SYNDIG1), mRNA.	224					response to biotic stimulus	early endosome membrane|integral to membrane|plasma membrane				breast(2)|endometrium(1)|large_intestine(3)|lung(14)|prostate(1)|skin(3)	24						ACCAGCTCCCGGCGGGCCCTA	0.587000														59			18		0	0	1	0	0
BAZ1B	9031	broad.mit.edu	37	7	72863961	72863961	+	Silent	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr7:72863961A>G	uc003tyc.3	-	14	3991	c.3639T>C	c.(3637-3639)tgT>tgC	p.C1213C		NM_032408	NP_115784	Q9UIG0	BAZ1B_HUMAN	Homo sapiens bromodomain adjacent to zinc finger domain, 1B (BAZ1B), mRNA.	1213					ATP-dependent chromatin remodeling|DNA replication-dependent nucleosome disassembly|chromatin-mediated maintenance of transcription|double-strand break repair|heart morphogenesis|transcription, DNA-dependent	WINAC complex	ATP binding|chromatin binding|histone acetyl-lysine binding|histone kinase activity|non-membrane spanning protein tyrosine kinase activity|protein complex scaffold|vitamin D receptor activator activity|vitamin D receptor binding|zinc ion binding			NS(1)|breast(5)|cervix(1)|endometrium(5)|kidney(5)|large_intestine(12)|lung(20)|ovary(5)|prostate(3)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	61		Lung NSC(55;0.0659)|all_lung(88;0.152)				CCGGCCTCAGACAAAACAGGT	0.517000														115			5		0	0	1	0	0
GYLTL1B	120071	broad.mit.edu	37	11	45945039	45945039	+	Missense_Mutation	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr11:45945039A>G	uc001nbv.1	+	2	412	c.301A>G	c.(301-303)Atc>Gtc	p.I101V	GYLTL1B_uc001nbw.1_Missense_Mutation_p.I70V|GYLTL1B_uc001nbx.1_Missense_Mutation_p.I101V	NM_152312	NP_689525	Q8N3Y3	LARG2_HUMAN	Homo sapiens glycosyltransferase-like 1B (GYLTL1B), mRNA.	101					muscle cell homeostasis	Golgi membrane|integral to membrane	transferase activity, transferring glycosyl groups			breast(2)|central_nervous_system(2)|endometrium(6)|large_intestine(4)|lung(5)|ovary(2)|upper_aerodigestive_tract(1)	22				GBM - Glioblastoma multiforme(35;0.226)		GCATGTGGCCATCGTGTGTGC	0.642000														35			5		0	0	1	0	0
MGC70870	403340	broad.mit.edu	37	GL000205.1	118544	118544	+	RNA	SNP	A	G	G			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chrGL000205.1:118544A>G	uc002kgk.4	+	0		c.1922A>G								Homo sapiens C-terminal binding protein 2 pseudogene (MGC70870), non-coding RNA.																		AGATAATCTAAGAGAAAAAGA	0.408000														19			3		0	0	1	0	0
LHX8	431707	broad.mit.edu	37	1	75622672	75622672	+	Missense_Mutation	SNP	T	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr1:75622672T>C	uc001dgo.3	+	8	1569	c.905T>C	c.(904-906)cTg>cCg	p.L302P	LHX8_uc001dgq.3_Missense_Mutation_p.L241P	NM_001001933	NP_001001933	Q68G74	LHX8_HUMAN	Homo sapiens LIM homeobox 8 (LHX8), transcript variant 1, mRNA.	302						nucleus	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			NS(1)|breast(1)|endometrium(1)|kidney(1)|large_intestine(4)|lung(18)|ovary(3)|urinary_tract(1)	30						CCCTCCAGGCTGTCTCCACCC	0.507000														72			4		0	0	1	0	0
FEZ1	9638	broad.mit.edu	37	11	125359542	125359542	+	Silent	SNP	G	A	A			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr11:125359542G>A	uc001qbx.3	-	1	367	c.132C>T	c.(130-132)tcC>tcT	p.S44S	FEZ1_uc010sbc.2_Silent_p.S44S|FEZ1_uc001qby.2_Silent_p.S44S|FEZ1_uc021qrv.1_Silent_p.S44S	NM_005103	NP_005094	Q99689	FEZ1_HUMAN	Homo sapiens fasciculation and elongation protein zeta 1 (zygin I) (FEZ1), transcript variant 1, mRNA.	44					axon guidance|cell adhesion|transport	microtubule|plasma membrane		p.L43I(1)		breast(1)|central_nervous_system(3)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(5)|lung(9)|ovary(1)|upper_aerodigestive_tract(1)	24	all_hematologic(175;0.228)	Breast(109;0.0021)|Lung NSC(97;0.0126)|all_lung(97;0.0132)|Medulloblastoma(222;0.0425)|all_neural(223;0.112)		BRCA - Breast invasive adenocarcinoma(274;1.49e-06)|OV - Ovarian serous cystadenocarcinoma(99;0.0934)		TCTCAAGCTCGGAGAGGGAGG	0.502000														90			24		0	0	1	0	0
OR10H2	26538	broad.mit.edu	37	19	15839690	15839690	+	Silent	SNP	C	T	T	rs141193809	by1000genomes	TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr19:15839690C>T	uc002nbm.2	+	0	857	c.837C>T	c.(835-837)taC>taT	p.Y279Y		NM_013939	NP_039227	O60403	O10H2_HUMAN	Homo sapiens olfactory receptor, family 10, subfamily H, member 2 (OR10H2), mRNA.	279					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			breast(2)|central_nervous_system(1)|endometrium(1)|kidney(1)|large_intestine(6)|lung(10)|ovary(2)|skin(3)|stomach(1)	27	all_hematologic(1;0.0517)|Acute lymphoblastic leukemia(2;0.074)					CCACCACCTACGCAGTCCTCA	0.532000														62			31		0	0	1	0	0
MGC70870	403340	broad.mit.edu	37	GL000205.1	118490	118490	+	RNA	SNP	G	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chrGL000205.1:118490G>T	uc002kgk.4	+	0		c.1868G>T								Homo sapiens C-terminal binding protein 2 pseudogene (MGC70870), non-coding RNA.																		AGCAGAGAATGCCGGAAGGTA	0.463000														38			3		0.00909568	0.00909568	1	1	0
ADAMTS14	140766	broad.mit.edu	37	10	72496471	72496471	+	Silent	SNP	C	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr10:72496471C>T	uc001jrg.3	+	9	1530	c.1530C>T	c.(1528-1530)tgC>tgT	p.C510C	ADAMTS14_uc001jrh.3_Silent_p.C507C|ADAMTS14_uc001jri.1_Silent_p.C30C	NM_139155	NP_631894	Q8WXS8	ATS14_HUMAN	Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif, 14 (ADAMTS14), transcript variant 1, mRNA.	507	Disintegrin.				collagen catabolic process|proteolysis	proteinaceous extracellular matrix	metalloendopeptidase activity|zinc ion binding			NS(1)|autonomic_ganglia(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(11)|lung(15)|ovary(7)|prostate(3)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(2)	50						AGCTGTGGTGCAGCCATCCTG	0.587000														41			3		0	0	1	0	0
GPR35	2859	broad.mit.edu	37	2	241570087	241570087	+	Missense_Mutation	SNP	C	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr2:241570087C>T	uc010fzi.2	+	5	1683	c.811C>T	c.(811-813)Cgc>Tgc	p.R271C	GPR35_uc010fzh.2_Missense_Mutation_p.R271C|GPR35_uc021vze.1_Missense_Mutation_p.R240C|GPR35_uc002vzs.2_Missense_Mutation_p.R240C	NM_001195381	NP_001182310	Q9HC97	GPR35_HUMAN	Homo sapiens G protein-coupled receptor 35 (GPR35), transcript variant 2, mRNA.	240						integral to plasma membrane	G-protein coupled receptor activity			NS(2)|breast(1)|cervix(1)|endometrium(1)|lung(7)|ovary(1)|pancreas(1)|skin(2)|urinary_tract(1)	17		all_epithelial(40;7.49e-12)|Breast(86;0.000148)|Renal(207;0.00571)|Ovarian(221;0.104)|all_neural(83;0.107)|all_hematologic(139;0.182)|all_lung(227;0.186)|Melanoma(123;0.238)		Epithelial(32;5.29e-32)|all cancers(36;1.38e-29)|OV - Ovarian serous cystadenocarcinoma(60;2.13e-15)|Kidney(56;3.04e-09)|KIRC - Kidney renal clear cell carcinoma(57;3.23e-08)|BRCA - Breast invasive adenocarcinoma(100;5.02e-06)|Lung(119;0.00163)|Colorectal(34;0.00463)|LUSC - Lung squamous cell carcinoma(224;0.008)|COAD - Colon adenocarcinoma(134;0.031)		GCTGACAGTGCGCCTCGCAGT	0.667000														6			28		0	0	1	0	0
GPX1	2876	broad.mit.edu	37	3	49395482	49395482	+	Missense_Mutation	SNP	G	C	C			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr3:49395482G>C	uc021wxw.1	-	0	310	c.230C>G	c.(229-231)cCg>cGg	p.P77R	GPX1_uc021wxx.1_Missense_Mutation_p.P77R	NM_000581	NP_000572	P07203	GPX1_HUMAN	Homo sapiens glutathione peroxidase 1 (GPX1), transcript variant 1, mRNA.	77					UV protection|anti-apoptosis|cell redox homeostasis|glutathione metabolic process|heart contraction|hydrogen peroxide catabolic process|negative regulation of caspase activity|purine base metabolic process|purine nucleotide catabolic process|regulation of gene expression, epigenetic|regulation of mammary gland epithelial cell proliferation|regulation of proteasomal protein catabolic process|release of cytochrome c from mitochondria|response to selenium ion	cytosol|mitochondrion	SH3 domain binding|endopeptidase inhibitor activity|glutathione peroxidase activity			breast(1)|large_intestine(2)|lung(1)	4				BRCA - Breast invasive adenocarcinoma(193;8.01e-05)|Kidney(197;0.00216)|KIRC - Kidney renal clear cell carcinoma(197;0.00244)	Glutathione(DB00143)	CTGGTTGCACGGGAAGCCGAG	0.726000														14			3		0	0	1	0	0
CELSR3	1951	broad.mit.edu	37	3	48697290	48697290	+	Silent	SNP	G	T	T			TCGA-KO-8414-01A-11D-2310-10	TCGA-KO-8414-11A-01D-2311-10								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	2a61c3d7-f0c1-45d1-9eca-02fb72e95c13	edf00a92-13fd-4c2f-b41c-16458d1a47dd	g.chr3:48697290G>T	uc003cuf.1	-	2	2988	c.2988C>A	c.(2986-2988)acC>acA	p.T996T	CELSR3_uc003cul.3_Silent_p.T926T	NM_001407	NP_001398	Q9NYQ7	CELR3_HUMAN	Homo sapiens cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) (CELSR3), mRNA.	926	Cadherin 7.				homophilic cell adhesion|multicellular organismal development|neuropeptide signaling pathway	integral to membrane|plasma membrane	G-protein coupled receptor activity|calcium ion binding|protein binding	p.R995W(1)		NS(1)|biliary_tract(1)|breast(2)|central_nervous_system(3)|cervix(1)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(7)|lung(23)|ovary(9)|prostate(6)|skin(7)|stomach(1)|upper_aerodigestive_tract(3)|urinary_tract(5)	83				BRCA - Breast invasive adenocarcinoma(193;0.000292)|KIRC - Kidney renal clear cell carcinoma(197;0.00549)|Kidney(197;0.00619)		CCAGGGTGTAGGTCACCTGGT	0.522000														147			4		0.00116845	0.00120739	1	1	0
