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	t_alt_count	t_ref_count	validation_alt_allele	validation_method	validation_status	validation_tumor_sample	pox	qox	pox_cutoff	isArtifactMode	oxoGCut
CA10	56934	broad.mit.edu	37	17	49710999	49710999	+	Missense_Mutation	SNP	G	G	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:49710999G>A	uc002itv.4	-	8	1556	c.820C>T	c.(820-822)Cgc>Tgc	p.R274C	CA10_uc002itw.4_Missense_Mutation_p.R268C|CA10_uc002itx.4_Missense_Mutation_p.R268C|CA10_uc002ity.4_Missense_Mutation_p.R268C|CA10_uc002itz.2_Missense_Mutation_p.R268C	NM_020178	NP_064563	Q9NS85	CAH10_HUMAN	Homo sapiens carbonic anhydrase X (CA10), transcript variant 2, mRNA.	268					brain development					cervix(1)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(4)|lung(21)|ovary(1)|skin(3)|stomach(2)|urinary_tract(1)	41			BRCA - Breast invasive adenocarcinoma(22;4.74e-06)			CTGAGCAGGCGCAAGGAATGC	0.512000													10	66					0	0	1	0	0
RPS6KA1	6195	broad.mit.edu	37	1	26883148	26883148	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr1:26883148C>T	uc001bmr.1	+	11	1083	c.920C>T	c.(919-921)tCc>tTc	p.S307F	RPS6KA1_uc010ofe.1_Missense_Mutation_p.S215F|RPS6KA1_uc010off.1_Missense_Mutation_p.S291F|RPS6KA1_uc001bms.1_Missense_Mutation_p.S316F|RPS6KA1_uc009vsl.1_Missense_Mutation_p.S150F	NM_002953	NP_002944	Q15418	KS6A1_HUMAN	Homo sapiens ribosomal protein S6 kinase, 90kDa, polypeptide 1 (RPS6KA1), transcript variant 1, mRNA.	307	Protein kinase 1.				MyD88-dependent toll-like receptor signaling pathway|MyD88-independent toll-like receptor signaling pathway|Toll signaling pathway|axon guidance|innate immune response|nerve growth factor receptor signaling pathway|stress-activated MAPK cascade|synaptic transmission|toll-like receptor 1 signaling pathway|toll-like receptor 2 signaling pathway|toll-like receptor 3 signaling pathway|toll-like receptor 4 signaling pathway	cytosol|nucleoplasm	ATP binding|caspase inhibitor activity|magnesium ion binding|protein binding|protein serine/threonine kinase activity			lung(1)	1		all_cancers(24;2.49e-24)|Colorectal(325;3.46e-05)|all_lung(284;4.76e-05)|Lung NSC(340;5.83e-05)|Renal(390;0.0007)|Ovarian(437;0.00473)|Breast(348;0.00571)|Myeloproliferative disorder(586;0.0255)|all_neural(195;0.0381)		UCEC - Uterine corpus endometrioid carcinoma (279;0.0178)|Epithelial(14;1.12e-50)|OV - Ovarian serous cystadenocarcinoma(117;2.89e-29)|Colorectal(126;1.4e-08)|COAD - Colon adenocarcinoma(152;9.31e-07)|BRCA - Breast invasive adenocarcinoma(304;0.000537)|KIRC - Kidney renal clear cell carcinoma(1967;0.000759)|STAD - Stomach adenocarcinoma(196;0.00151)|GBM - Glioblastoma multiforme(114;0.0361)|READ - Rectum adenocarcinoma(331;0.0649)|Lung(427;0.161)|LUSC - Lung squamous cell carcinoma(448;0.234)		CTTTCAGGCTCCGGCCCTGAT	0.592000													20	52					0	0	1	0	0
TTN	7273	broad.mit.edu	37	2	179554578	179554578	+	Missense_Mutation	SNP	A	A	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr2:179554578A>G	uc021vsy.1	-	118	28301	c.28076T>C	c.(28075-28077)gTt>gCt	p.V9359A	TTN_uc021vsz.1_Intron|TTN_uc021vta.1_Intron|TTN_uc021vtb.1_Intron|TTN_uc002umz.1_Missense_Mutation_p.V6020A|TTN_uc010fre.1_Missense_Mutation_p.V470A	NM_133378	NP_596869	Q8WZ42	TITIN_HUMAN	Homo sapiens titin (TTN), transcript variant N2-A, mRNA.	10286	Ig-like 76.						ATP binding|nucleic acid binding|protein serine/threonine kinase activity|protein tyrosine kinase activity			NS(24)|autonomic_ganglia(1)|breast(64)|central_nervous_system(14)|cervix(14)|endometrium(96)|haematopoietic_and_lymphoid_tissue(16)|kidney(91)|large_intestine(303)|liver(1)|lung(595)|ovary(58)|pancreas(17)|prostate(38)|skin(60)|stomach(29)|upper_aerodigestive_tract(1)|urinary_tract(26)	1448			OV - Ovarian serous cystadenocarcinoma(117;0.023)|Epithelial(96;0.0454)|all cancers(119;0.134)			TGCAACAGGAACGGGAATCTT	0.378000													13	169					0	0	1	0	0
LOC650368	650368	broad.mit.edu	37	11	3427845	3427845	+	RNA	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr11:3427845C>T	uc010qxs.1	+	8		c.838C>T			LOC650368_uc001lxy.2_Non-coding_Transcript					Homo sapiens asparagine-linked glycosylation 1-like pseudogene (LOC650368), non-coding RNA.																		CTTCAAGTGGCAGGAGCAGAA	0.587000													5	52					0	0	1	0	0
LILRA5	353514	broad.mit.edu	37	19	54822890	54822890	+	Missense_Mutation	SNP	T	T	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:54822890T>G	uc002qfe.3	-	4	626	c.506A>C	c.(505-507)gAc>gCc	p.D169A	LILRA5_uc002qff.3_Missense_Mutation_p.D157A|LILRA5_uc010yev.2_Missense_Mutation_p.D169A|LILRA5_uc010yew.2_Missense_Mutation_p.D157A|LILRA5_uc002qfg.1_Missense_Mutation_p.D169A|LILRA5_uc002qfh.1_Missense_Mutation_p.D157A	NM_021250	NP_067073	A6NI73	LIRA5_HUMAN	Homo sapiens leukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 5 (LILRA5), transcript variant 1, mRNA.	169	Ig-like C2-type 2.				innate immune response	extracellular region|integral to membrane	receptor activity			breast(1)|endometrium(2)|large_intestine(4)|lung(6)|ovary(1)|prostate(2)|upper_aerodigestive_tract(3)|urinary_tract(1)	20	Ovarian(34;0.19)			GBM - Glioblastoma multiforme(193;0.105)		AATGAACCTGTCGAATCTCAG	0.587000													34	58					0	0	1	0	0
FAT2	2196	broad.mit.edu	37	5	150923936	150923936	+	Missense_Mutation	SNP	C	C	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr5:150923936C>G	uc003lue.4	-	8	6765	c.6752G>C	c.(6751-6753)gGg>gCg	p.G2251A		NM_001447	NP_001438	Q9NYQ8	FAT2_HUMAN	Homo sapiens FAT tumor suppressor homolog 2 (Drosophila) (FAT2), mRNA.	2251	Cadherin 19.				epithelial cell migration|homophilic cell adhesion	cell-cell adherens junction|integral to membrane|nucleus	calcium ion binding			NS(6)|breast(3)|central_nervous_system(3)|cervix(5)|endometrium(15)|haematopoietic_and_lymphoid_tissue(4)|kidney(8)|large_intestine(61)|liver(1)|lung(60)|ovary(6)|prostate(5)|skin(5)|stomach(2)|upper_aerodigestive_tract(11)|urinary_tract(1)	196		Medulloblastoma(196;0.0912)|all_hematologic(541;0.104)	KIRC - Kidney renal clear cell carcinoma(527;0.000785)|Kidney(363;0.00101)			AGAAAATGACCCCAGAGCTGT	0.478000													13	41					0	0	1	0	0
SBSN	374897	broad.mit.edu	37	19	36018836	36018836	+	Silent	SNP	G	G	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:36018836G>A	uc002oad.2	-	0	418	c.348C>T	c.(346-348)ggC>ggT	p.G116G	SBSN_uc002oae.2_Silent_p.G116G|SBSN_uc021usp.1_Silent_p.G116G	NM_001166034	NP_001159506	Q6UWP8	SBSN_HUMAN	Homo sapiens suprabasin (SBSN), transcript variant 1, mRNA.	116	Ala/Gly/His-rich.					extracellular region				large_intestine(5)|lung(6)|ovary(1)|prostate(2)	14	all_lung(56;1.62e-08)|Lung NSC(56;2.47e-08)|Esophageal squamous(110;0.162)		LUSC - Lung squamous cell carcinoma(66;0.0724)			TGACCCCATGGCCAAGCTTCT	0.572000													10	170					0	0	1	0	0
ARHGEF1	9138	broad.mit.edu	37	19	42409353	42409353	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:42409353C>T	uc002orx.3	+	23	2385	c.2276C>T	c.(2275-2277)gCc>gTc	p.A759V	ARHGEF1_uc002ory.3_Missense_Mutation_p.A726V|ARHGEF1_uc002orz.3_Missense_Mutation_p.A597V|ARHGEF1_uc002osa.3_Missense_Mutation_p.A774V|ARHGEF1_uc002osb.3_Missense_Mutation_p.A741V|ARHGEF1_uc002osc.3_Missense_Mutation_p.A513V|ARHGEF1_uc002osd.3_Missense_Mutation_p.A418V	NM_004706	NP_004697	Q92888	ARHG1_HUMAN	Homo sapiens Rho guanine nucleotide exchange factor (GEF) 1 (ARHGEF1), transcript variant 2, mRNA.	759	PH.				Rho protein signal transduction|cell proliferation|negative regulation of axonogenesis|nerve growth factor receptor signaling pathway|positive regulation of axonogenesis|regulation of Rho protein signal transduction	cytosol|plasma membrane	GTPase activator activity|Rho guanyl-nucleotide exchange factor activity|protein binding			breast(2)|endometrium(8)|large_intestine(6)|lung(9)|ovary(3)|prostate(1)|skin(4)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	37		Renal(1328;0.000518)|Hepatocellular(1079;0.0046)|Medulloblastoma(540;0.0425)		Epithelial(262;5.89e-46)|GBM - Glioblastoma multiforme(1328;2.49e-12)|STAD - Stomach adenocarcinoma(1328;0.00644)		ACTGAGACTGCCGGATCCCTG	0.662000													4	89					0	0	1	0	0
BC101079	0	broad.mit.edu	37	15	102292797	102292797	+	Missense_Mutation	SNP	C	C	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr15:102292797C>G	uc010usj.2	+	3	444	c.385C>G	c.(385-387)Cca>Gca	p.P129A	DQ597539_uc002bxo.3_Non-coding_Transcript|DQ593624_uc002bxp.4_5'Flank|DQ576888_uc021sxy.1_5'Flank|DQ596486_uc002bxz.4_5'Flank|DQ582294_uc021syc.1_5'Flank|DQ595661_uc021sye.1_5'Flank|DQ588439_uc002byd.3_5'Flank|DQ593353_uc002bye.3_5'Flank|DQ597703_uc002byf.1_5'Flank|DQ585237_uc002byg.3_5'Flank|DQ588452_uc021syg.1_5'Flank|DQ586526_uc002byi.3_5'Flank|DQ588428_uc002byk.3_5'Flank|DQ597703_uc002bym.3_5'Flank|DQ571896_uc010usm.2_5'Flank|DQ586526_uc021syh.1_5'Flank|DQ588425_uc002byr.3_5'Flank					Homo sapiens cDNA clone IMAGE:40009338.									p.P129A(2)									GAGCTGCTGTCCAACCTGCAC	0.597000													3	34					0	0	1	0	0
GPS1	2873	broad.mit.edu	37	17	80013939	80013939	+	Silent	SNP	G	G	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:80013939G>A	uc002kdk.1	+	7	1437	c.1017G>A	c.(1015-1017)cgG>cgA	p.R339R	GPS1_uc002kdl.1_Silent_p.R303R|GPS1_uc010dij.1_Silent_p.R338R|GPS1_uc002kdm.1_Silent_p.R283R|GPS1_uc002kdn.1_Silent_p.R299R|GPS1_uc010wvh.1_Silent_p.R295R	NM_212492	NP_997657	Q13098	CSN1_HUMAN	Homo sapiens G protein pathway suppressor 1 (GPS1), transcript variant 1, mRNA.	303	PCI.				JNK cascade|cell cycle|cullin deneddylation|inactivation of MAPK activity	cytoplasm|signalosome	GTPase inhibitor activity|protein binding			breast(1)|central_nervous_system(1)|endometrium(3)|liver(1)|lung(4)|prostate(1)|skin(2)	13	all_neural(118;0.0878)|Ovarian(332;0.227)|all_lung(278;0.246)		BRCA - Breast invasive adenocarcinoma(99;0.0114)|OV - Ovarian serous cystadenocarcinoma(97;0.0211)			CCTTTGACCGGCAGGAGCTGC	0.652000													4	39					0	0	1	0	0
ARHGAP11B	89839	broad.mit.edu	37	15	30938316	30938316	+	Splice_Site	SNP	G	G	A	rs112615235	by1000genomes	TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr15:30938316G>A	uc010azv.1	+	11		c.1127_splice	c.e11-1		ARHGAP11B_uc001zeu.3_Splice_Site|LOC100288637_uc001zev.3_5'Flank			Q3KRB8	RHGBB_HUMAN	Homo sapiens Rho GTPase activating protein 11B (ARHGAP11B), mRNA.						regulation of small GTPase mediated signal transduction|small GTPase mediated signal transduction	cytosol	GTPase activator activity			endometrium(2)|kidney(1)|large_intestine(3)|lung(1)|prostate(1)	8		all_lung(180;2.71e-09)|Breast(32;0.00116)		all cancers(64;1.9e-15)|Epithelial(43;3.59e-12)|GBM - Glioblastoma multiforme(186;9e-05)|BRCA - Breast invasive adenocarcinoma(123;0.00177)|Lung(196;0.153)		TTCCTTGGCAGTGGATAAGTT	0.393000													3	29					0	0	1	0	0
KIF1A	547	broad.mit.edu	37	2	241689870	241689870	+	Missense_Mutation	SNP	G	G	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr2:241689870G>A	uc010fzk.3	-	27	3200	c.2953C>T	c.(2953-2955)Cgc>Tgc	p.R985C	KIF1A_uc002vzy.3_Missense_Mutation_p.R884C|KIF1A_uc002vzz.2_Missense_Mutation_p.R985C	NM_001244008	NP_001230937	Q12756	KIF1A_HUMAN	Homo sapiens kinesin family member 1A (KIF1A), transcript variant 1, mRNA.	884					anterograde axon cargo transport	cytoplasm|microtubule|nucleus	ATP binding|microtubule motor activity	p.D984G(1)		NS(1)|central_nervous_system(2)|endometrium(14)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(8)|lung(25)|ovary(1)|prostate(5)|skin(2)|urinary_tract(1)	66		all_epithelial(40;1.35e-15)|Breast(86;2.14e-05)|Renal(207;0.00183)|Ovarian(221;0.0228)|all_lung(227;0.0295)|all_neural(83;0.0459)|Lung NSC(271;0.0942)|all_hematologic(139;0.158)|Melanoma(123;0.16)|Hepatocellular(293;0.244)		Epithelial(32;6.12e-30)|all cancers(36;3.46e-27)|OV - Ovarian serous cystadenocarcinoma(60;1.38e-14)|Kidney(56;5e-09)|KIRC - Kidney renal clear cell carcinoma(57;5e-08)|BRCA - Breast invasive adenocarcinoma(100;5.87e-06)|Lung(119;0.00209)|LUSC - Lung squamous cell carcinoma(224;0.00902)|Colorectal(34;0.0282)|COAD - Colon adenocarcinoma(134;0.176)		ACGGCCACGCGGAGGAAGCCC	0.657000													9	40					0	0	1	0	0
TNFAIP1	7126	broad.mit.edu	37	17	26666643	26666643	+	Silent	SNP	C	C	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:26666643C>A	uc002hax.2	+	1	115	c.96C>A	c.(94-96)ctC>ctA	p.L32L	TNFAIP1_uc002hay.3_Silent_p.L32L|TNFAIP1_uc010waf.2_Intron	NM_021137	NP_066960	Q13829	BACD2_HUMAN	Homo sapiens tumor necrosis factor, alpha-induced protein 1 (endothelial) (TNFAIP1), mRNA.	32	BTB.				DNA replication|apoptosis|cell migration|embryo development|immune response|negative regulation of Rho protein signal transduction|proteasomal ubiquitin-dependent protein catabolic process|protein ubiquitination|stress fiber assembly	Cul3-RING ubiquitin ligase complex|endosome|nucleus|voltage-gated potassium channel complex	GTP-Rho binding|voltage-gated potassium channel activity			endometrium(3)|kidney(1)|large_intestine(4)|lung(3)|prostate(1)	12	all_lung(13;0.000294)|Lung NSC(42;0.000964)			UCEC - Uterine corpus endometrioid carcinoma (53;0.153)		ATGTCCAGCTCAACGTGGGCG	0.637000													24	64					0	0	1	0	0
ZBTB4	57659	broad.mit.edu	37	17	7366351	7366351	+	Missense_Mutation	SNP	C	C	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:7366351C>A	uc002ghc.4	-	3	2200	c.1950G>T	c.(1948-1950)gaG>gaT	p.E650D	ZBTB4_uc002ghd.4_Missense_Mutation_p.E650D	NM_001128833	NP_065950	Q9P1Z0	ZBTB4_HUMAN	Homo sapiens zinc finger and BTB domain containing 4 (ZBTB4), transcript variant 2, mRNA.	650	Glu-rich.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			NS(1)|breast(1)|central_nervous_system(1)|cervix(2)|endometrium(7)|kidney(1)|large_intestine(4)|lung(7)|ovary(3)|prostate(3)|skin(6)	36		Colorectal(1115;3.46e-05)|Myeloproliferative disorder(207;0.0255)		COAD - Colon adenocarcinoma(228;4.1e-06)|READ - Rectum adenocarcinoma(115;0.0642)		cctcctcatcctcctcctcct	0.607000													4	41					0	0	1	0	0
IDH1	3417	broad.mit.edu	37	2	209113113	209113113	+	Missense_Mutation	SNP	G	G	A	rs121913499		TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr2:209113113G>A	uc002vcs.3	-	3	640	c.394C>T	c.(394-396)Cgt>Tgt	p.R132C	IDH1_uc002vct.3_Missense_Mutation_p.R132C|IDH1_uc002vcu.3_Missense_Mutation_p.R132C	NM_005896	NP_005887	O75874	IDHC_HUMAN	Homo sapiens isocitrate dehydrogenase 1 (NADP+), soluble (IDH1), mRNA.	132			R -> C (in colorectal cancer and glioma samples; glioblastoma multiforme; somatic mutation; abolishes magnesium binding and alters enzyme activity so that isocitrate is no longer converted to alpha- ketoglutarate but instead alpha- ketoglutarate is converted to R(-)-2- hydroxyglutarate).|R -> G (in a glioma sample; glioblastoma multiforme; somatic mutation).|R -> H (in a glioma sample; glioblastoma multiforme; somatic mutation; abolishes magnesium binding and alters enzyme activity so that isocitrate is no longer converted to alpha-ketoglutarate but instead alpha-ketoglutarate is converted to R(-)-2-hydroxyglutarate).|R -> L (in a glioma sample; glioblastoma multiforme; somatic mutation; abolishes magnesium binding and alters enzyme activity so that isocitrate is no longer converted to alpha-ketoglutarate but instead alpha-ketoglutarate is converted to R(-)-2-hydroxyglutarate).|R -> S (in a glioma sample; glioblastoma multiforme; somatic mutation; abolishes magnesium binding and alters enzyme activity so that isocitrate is no longer converted to alpha-ketoglutarate but instead alpha-ketoglutarate is converted to R(-)-2-hydroxyglutarate).		2-oxoglutarate metabolic process|NADPH regeneration|cellular lipid metabolic process|glyoxylate cycle|isocitrate metabolic process|tricarboxylic acid cycle	cytosol|peroxisomal matrix	NAD binding|isocitrate dehydrogenase (NADP+) activity|magnesium ion binding|protein homodimerization activity	p.R132H(3651)|p.R132C(1036)|p.R132G(298)|p.R132S(246)|p.R132?(189)|p.R132L(71)|p.R132V(2)|p.G131_R132>VL(2)|p.R132P(1)		NS(1)|autonomic_ganglia(2)|biliary_tract(24)|bone(237)|central_nervous_system(3764)|endometrium(3)|haematopoietic_and_lymphoid_tissue(794)|kidney(2)|large_intestine(7)|lung(7)|prostate(6)|skin(5)|soft_tissue(12)|thyroid(22)|urinary_tract(1)	4887				Epithelial(149;0.0322)|LUSC - Lung squamous cell carcinoma(261;0.0711)|Lung(261;0.136)		TAAGCATGACGACCTATGATG	0.398000			Mis		gliobastoma								15	40					0	0	1	0	0
C19orf47	126526	broad.mit.edu	37	19	40828229	40828229	+	Missense_Mutation	SNP	C	C	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:40828229C>A	uc002oni.4	-	8	830	c.829G>T	c.(829-831)Gct>Tct	p.A277S	C19orf47_uc002ong.3_Missense_Mutation_p.A136S|C19orf47_uc002onh.3_Missense_Mutation_p.A210S	NM_178830	NP_849152	Q8N9M1	CS047_HUMAN	Homo sapiens chromosome 19 open reading frame 47 (C19orf47), mRNA.	277								p.P277L(2)|p.P277S(1)		endometrium(5)|kidney(2)|lung(7)|ovary(3)|prostate(1)|skin(1)|urinary_tract(1)	20			Lung(22;0.000636)			CTGTCCCAAGCCAGATCCTCG	0.612000													16	35					0	0	1	0	0
LRRIQ1	84125	broad.mit.edu	37	12	85450803	85450803	+	Silent	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr12:85450803C>T	uc001tac.3	+	7	2343	c.2232C>T	c.(2230-2232)gcC>gcT	p.A744A	LRRIQ1_uc021rbo.1_Silent_p.A622A|LRRIQ1_uc001taa.1_Silent_p.A719A	NM_001079910	NP_001073379	Q96JM4	LRIQ1_HUMAN	Homo sapiens leucine-rich repeats and IQ motif containing 1 (LRRIQ1), mRNA.	744										breast(1)|central_nervous_system(1)|cervix(1)|endometrium(6)|haematopoietic_and_lymphoid_tissue(2)|kidney(4)|large_intestine(21)|liver(1)|lung(28)|ovary(5)|prostate(1)|skin(8)|stomach(2)|upper_aerodigestive_tract(2)	83				GBM - Glioblastoma multiforme(134;0.212)		GGAGACTAGCCTGGATAAAAT	0.368000													101	225					0	0	1	0	0
TCEB3B	51224	broad.mit.edu	37	18	44560758	44560758	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr18:44560758C>T	uc002lcr.1	-	0	1231	c.878G>A	c.(877-879)cGt>cAt	p.R293H	KATNAL2_uc010dnq.1_Intron|KATNAL2_uc002lco.3_Intron	NM_016427	NP_057511	Q8IYF1	ELOA2_HUMAN	Homo sapiens transcription elongation factor B polypeptide 3B (elongin A2) (TCEB3B), mRNA.	293					regulation of transcription elongation, DNA-dependent|transcription from RNA polymerase II promoter	integral to membrane|nucleus	DNA binding			breast(1)|cervix(3)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(15)|lung(24)|ovary(2)|pancreas(2)|prostate(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	58						GGCAGGGACACGCTGGCCGCT	0.627000													51	92					0	0	1	0	0
DNAH17	8632	broad.mit.edu	37	17	76563157	76563157	+	Missense_Mutation	SNP	C	C	T	rs143602861	byFrequency	TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:76563157C>T	uc010dhp.2	-	9	1501	c.1376G>A	c.(1375-1377)cGt>cAt	p.R459H	DNAH17_uc002jvv.2_Missense_Mutation_p.R161H	NM_173628	NP_775899			Homo sapiens dynein, axonemal, heavy chain 17 (DNAH17), mRNA.											NS(2)|breast(7)|central_nervous_system(5)|cervix(1)|endometrium(15)|haematopoietic_and_lymphoid_tissue(1)|kidney(13)|large_intestine(8)|lung(37)|ovary(8)|prostate(7)|skin(4)|stomach(2)|upper_aerodigestive_tract(3)|urinary_tract(3)	116			BRCA - Breast invasive adenocarcinoma(99;0.00294)|OV - Ovarian serous cystadenocarcinoma(97;0.0656)			ATCATAGATACGGGTCACCAG	0.527000													3	28					0	0	1	0	0
FLJ43315	644316	broad.mit.edu	37	GL000211.1	107044	107044	+	RNA	SNP	T	T	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chrGL000211.1:107044T>C	uc003boa.3	+	3		c.743T>C								Homo sapiens asparagine synthetase pseudogene (FLJ43315), non-coding RNA.																		ACAAAGAAAATAGAACGCCTT	0.358000													4	218					0	0	1	0	0
NIPBL	25836	broad.mit.edu	37	5	37038775	37038775	+	Missense_Mutation	SNP	A	A	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr5:37038775A>G	uc003jkl.4	+	33	6542	c.6043A>G	c.(6043-6045)Ata>Gta	p.I2015V	NIPBL_uc003jkk.4_Missense_Mutation_p.I2015V	NM_133433	NP_597677	Q6KC79	NIPBL_HUMAN	Homo sapiens Nipped-B homolog (Drosophila) (NIPBL), transcript variant A, mRNA.	2015					brain development|cellular protein localization|cellular response to X-ray|cognition|developmental growth|ear morphogenesis|embryonic arm morphogenesis|embryonic digestive tract morphogenesis|external genitalia morphogenesis|eye morphogenesis|face morphogenesis|gall bladder development|maintenance of mitotic sister chromatid cohesion|metanephros development|negative regulation of transcription from RNA polymerase II promoter|outflow tract morphogenesis|positive regulation of histone deacetylation|regulation of developmental growth|regulation of embryonic development|regulation of hair cycle|response to DNA damage stimulus|sensory perception of sound|uterus morphogenesis	SMC loading complex	chromo shadow domain binding|histone deacetylase binding|protein C-terminus binding|protein N-terminus binding			autonomic_ganglia(1)|breast(4)|endometrium(9)|kidney(22)|large_intestine(21)|liver(1)|lung(47)|ovary(7)|pancreas(1)|prostate(1)|skin(7)|upper_aerodigestive_tract(3)|urinary_tract(4)	128	all_lung(31;0.000447)|Hepatocellular(1;0.108)		Epithelial(62;0.072)|COAD - Colon adenocarcinoma(61;0.14)|all cancers(62;0.191)|Colorectal(62;0.202)			ATTCAGCAAAATAAGACCCCA	0.363000													11	25					0	0	1	0	0
TRIM67	440730	broad.mit.edu	37	1	231333193	231333193	+	Missense_Mutation	SNP	A	A	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr1:231333193A>G	uc009xfn.1	+	1	1163	c.1121A>G	c.(1120-1122)aAc>aGc	p.N374S		NM_001004342	NP_001004342	Q6ZTA4	TRI67_HUMAN	Homo sapiens tripartite motif containing 67 (TRIM67), mRNA.	374						cytoplasm|cytoskeleton	zinc ion binding			breast(3)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(6)|lung(10)|ovary(2)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	29	Breast(184;0.0871)	all_cancers(173;0.189)|Prostate(94;0.167)				CAGCTAAAGAACATATTGCAG	0.433000													3	67					0	0	1	0	0
C16orf57	79650	broad.mit.edu	37	16	58036476	58036476	+	Silent	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr16:58036476C>T	uc002emz.3	+	1	303	c.192C>T	c.(190-192)agC>agT	p.S64S	ZNF319_uc002emx.1_5'Flank|C16orf57_uc002emy.3_Non-coding_Transcript|C16orf57_uc010via.2_Silent_p.S64S|C16orf57_uc010vib.2_Silent_p.S64S|C16orf57_uc010vic.1_Silent_p.S13S	NM_024598	NP_078874	Q9BQ65	CP057_HUMAN	Homo sapiens chromosome 16 open reading frame 57 (C16orf57), transcript variant 1, mRNA.	64										haematopoietic_and_lymphoid_tissue(1)|large_intestine(1)|lung(5)|skin(1)	8						AAGATGACAGCACAAAACACG	0.592000													40	36					0	0	1	0	0
MGC70870	403340	broad.mit.edu	37	GL000205.1	118268	118268	+	RNA	SNP	G	G	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chrGL000205.1:118268G>C	uc002kgk.4	+	0		c.1646G>C								Homo sapiens C-terminal binding protein 2 pseudogene (MGC70870), non-coding RNA.																		AAACCAGCAAGAAATTCATCC	0.512000													3	22					0	0	1	0	0
MUC16	94025	broad.mit.edu	37	19	9091118	9091118	+	Missense_Mutation	SNP	G	G	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:9091118G>T	uc002mkp.3	-	0	901	c.697C>A	c.(697-699)Ctt>Att	p.L233I		NM_024690	NP_078966	Q8WXI7	MUC16_HUMAN	Homo sapiens mucin 16, cell surface associated (MUC16), mRNA.	233	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						GAAGAATAAAGTGTCCCAAAT	0.463000													5	68					0	0	1	0	0
PI4KB	5298	broad.mit.edu	37	1	151288289	151288289	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr1:151288289C>T	uc001exr.3	-	2	1344	c.705G>A	c.(703-705)atG>atA	p.M235I	PI4KB_uc001exs.3_Missense_Mutation_p.M223I|PI4KB_uc001exu.3_Missense_Mutation_p.M223I|PI4KB_uc010pcw.2_Intron|PI4KB_uc001ext.3_Missense_Mutation_p.M223I	NM_002651	NP_001185704	Q9UBF8	PI4KB_HUMAN	Homo sapiens phosphatidylinositol 4-kinase, catalytic, beta (PI4KB), transcript variant 1, mRNA.	223					phosphatidylinositol biosynthetic process|phosphatidylinositol-mediated signaling|receptor-mediated endocytosis	Golgi apparatus|endosome|mitochondrial outer membrane|perinuclear region of cytoplasm|rough endoplasmic reticulum membrane	1-phosphatidylinositol 4-kinase activity|ATP binding|protein binding			breast(3)|endometrium(5)|kidney(3)|large_intestine(2)|lung(7)|ovary(2)|prostate(1)|skin(3)|upper_aerodigestive_tract(1)	27	Lung SC(34;0.00471)|Ovarian(49;0.0147)|Hepatocellular(266;0.0997)|all_hematologic(923;0.127)|Melanoma(130;0.185)		UCEC - Uterine corpus endometrioid carcinoma (35;0.112)|LUSC - Lung squamous cell carcinoma(543;0.181)			TGGAAATGTGCATGTCTGAAG	0.542000													23	34					0	0	1	0	0
SSTR5	6755	broad.mit.edu	37	16	1129911	1129911	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr16:1129911C>T	uc021taf.1	+	1	1114	c.1043C>T	c.(1042-1044)cCa>cTa	p.P348L	LOC146336_uc002cko.3_5'Flank|LOC146336_uc002ckp.1_5'Flank|SSTR5_uc002ckq.3_Missense_Mutation_p.P348L	NM_001172560	NP_001166031	P35346	SSR5_HUMAN	Homo sapiens somatostatin receptor 5 (SSTR5), transcript variant 2, mRNA.	348				PPAHR -> RPRT (in Ref. 1; AAA20828).	negative regulation of cell proliferation	integral to plasma membrane	somatostatin receptor activity			endometrium(2)|lung(5)|prostate(1)|skin(1)	9		Hepatocellular(780;0.00369)			Octreotide(DB00104)	GAGGCCACGCCACCCGCGCAC	0.701000													3	12					0	0	1	0	0
DCAF12L2	340578	broad.mit.edu	37	X	125299264	125299264	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chrX:125299264C>T	uc004euk.2	-	0	817	c.644G>A	c.(643-645)gGc>gAc	p.G215D		NM_001013628	NP_001013650	Q5VW00	DC122_HUMAN	Homo sapiens DDB1 and CUL4 associated factor 12-like 2 (DCAF12L2), mRNA.	215										NS(2)|central_nervous_system(1)|cervix(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(11)|lung(36)|ovary(2)|pancreas(1)|skin(2)|upper_aerodigestive_tract(3)	64						AGCCACGGTGCCGTCGCGGGA	0.642000													10	22					0	0	1	0	0
AKR1D1	6718	broad.mit.edu	37	7	137790074	137790074	+	Missense_Mutation	SNP	G	G	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr7:137790074G>C	uc003vtz.3	+	4	565	c.478G>C	c.(478-480)Gct>Cct	p.A160P	AKR1D1_uc011kqd.1_Non-coding_Transcript|AKR1D1_uc011kqb.1_Missense_Mutation_p.A160P|AKR1D1_uc011kqc.1_Non-coding_Transcript|AKR1D1_uc011kqf.2_Intron|AKR1D1_uc011kqe.1_Missense_Mutation_p.A160P|AKR1D1_uc010lmy.1_Non-coding_Transcript	NM_005989	NP_005980	P51857	AK1D1_HUMAN	Homo sapiens aldo-keto reductase family 1, member D1 (delta 4-3-ketosteroid-5-beta-reductase) (AKR1D1), transcript variant 1, mRNA.	160					C21-steroid hormone metabolic process|androgen metabolic process|bile acid biosynthetic process|bile acid catabolic process|cholesterol catabolic process|digestion	cytosol	aldo-keto reductase (NADP) activity|delta4-3-oxosteroid 5beta-reductase activity|steroid binding			endometrium(1)|kidney(2)|large_intestine(1)|lung(14)|ovary(1)|skin(3)|upper_aerodigestive_tract(1)	23						TTGCAAAGACGCTGGCTTGGT	0.478000													61	113					0	0	1	0	0
RBPJL	11317	broad.mit.edu	37	20	43943137	43943137	+	Missense_Mutation	SNP	C	C	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr20:43943137C>A	uc002xns.3	+	8	1024	c.952C>A	c.(952-954)Cca>Aca	p.P318T	RBPJL_uc002xnt.3_Missense_Mutation_p.P318T	NM_014276	NP_055091	Q9UBG7	RBPJL_HUMAN	Homo sapiens recombination signal binding protein for immunoglobulin kappa J region-like (RBPJL), mRNA.	318					signal transduction	nucleus	DNA binding|sequence-specific DNA binding transcription factor activity			NS(1)|breast(2)|kidney(1)|large_intestine(5)|lung(3)|ovary(2)|prostate(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	19		Myeloproliferative disorder(115;0.0122)				ATTCCAGTTTCCAGGCAGTCC	0.522000													4	123					0	0	1	0	0
MUC16	94025	broad.mit.edu	37	19	9057963	9057963	+	Missense_Mutation	SNP	G	G	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr19:9057963G>A	uc002mkp.3	-	2	29687	c.29483C>T	c.(29482-29484)tCc>tTc	p.S9828F		NM_024690	NP_078966	Q8WXI7	MUC16_HUMAN	Homo sapiens mucin 16, cell surface associated (MUC16), mRNA.	9830	Ser-rich.|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						TAGGACAGAGGAATGAGATTC	0.463000													38	66					0	0	1	0	0
FLJ43860	389690	broad.mit.edu	37	8	142505558	142505558	+	Missense_Mutation	SNP	G	G	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr8:142505558G>T	uc003ywi.2	-	2	369	c.288C>A	c.(286-288)gaC>gaA	p.D96E	FLJ43860_uc011ljs.1_5'Flank|FLJ43860_uc010meu.1_5'Flank	NM_207414	NP_997297	Q6ZUA9	Q6ZUA9_HUMAN	Homo sapiens FLJ43860 protein (FLJ43860), mRNA.	96							binding					all_cancers(97;7.79e-15)|all_epithelial(106;4.52e-13)|Lung NSC(106;2.07e-05)|all_lung(105;2.89e-05)|Ovarian(258;0.0303)|Acute lymphoblastic leukemia(118;0.155)		BRCA - Breast invasive adenocarcinoma(115;0.0493)			CACTGTTCATGTCCTGCAGCA	0.537000													21	43					0	0	1	0	0
ATG2A	23130	broad.mit.edu	37	11	64669827	64669827	+	Missense_Mutation	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr11:64669827C>T	uc001obx.3	-	27	3924	c.3809G>A	c.(3808-3810)tGc>tAc	p.C1270Y	ATG2A_uc001obw.3_Missense_Mutation_p.C35Y	NM_015104	NP_055919	Q2TAZ0	ATG2A_HUMAN	Homo sapiens ATG2 autophagy related 2 homolog A (S. cerevisiae) (ATG2A), mRNA.	1270							protein binding			breast(3)|central_nervous_system(3)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(8)|lung(19)|ovary(3)|prostate(5)|skin(1)|stomach(1)|urinary_tract(3)	55						CACTGGGGGGCACGAGGGCAG	0.687000													9	10					0	0	1	0	0
WRNIP1	56897	broad.mit.edu	37	6	2770371	2770371	+	Silent	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr6:2770371C>T	uc003mtz.3	+	2	1223	c.1032C>T	c.(1030-1032)caC>caT	p.H344H	WRNIP1_uc003mua.3_Intron	NM_020135	NP_064520	Q96S55	WRIP1_HUMAN	Homo sapiens Werner helicase interacting protein 1 (WRNIP1), transcript variant 1, mRNA.	344					DNA replication|DNA synthesis involved in DNA repair|regulation of DNA-dependent DNA replication initiation	mitochondrion|nucleus|perinuclear region of cytoplasm	ATP binding|ATPase activity|DNA binding|metal ion binding|protein binding			breast(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(2)|kidney(2)|large_intestine(1)|lung(2)|ovary(2)|pancreas(1)|prostate(1)|upper_aerodigestive_tract(1)	14	Ovarian(93;0.0412)	all_hematologic(90;0.0895)				TCCTTCCTCACGTGGAATGTG	0.488000													24	51					0	0	1	0	0
KIAA2026	158358	broad.mit.edu	37	9	5920338	5920338	+	Silent	SNP	A	A	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr9:5920338A>T	uc003zjq.4	-	7	5874	c.5658T>A	c.(5656-5658)ccT>ccA	p.P1886P	KIAA2026_uc010mht.3_Silent_p.P1061P	NM_001017969	NP_001017969	Q5HYC2	K2026_HUMAN	Homo sapiens KIAA2026 (KIAA2026), mRNA.	1886										breast(6)|central_nervous_system(1)|cervix(1)|endometrium(6)|kidney(1)|large_intestine(11)|lung(15)|ovary(2)|prostate(2)|skin(1)	46		Acute lymphoblastic leukemia(23;0.158)		GBM - Glioblastoma multiforme(50;0.00155)|Lung(218;0.124)		TCTGAGTACCAGGTGCCAAAG	0.428000													4	185					0	0	1	0	0
XPNPEP2	7512	broad.mit.edu	37	X	128901598	128901598	+	Missense_Mutation	SNP	C	C	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chrX:128901598C>G	uc004eut.1	+	19	2004	c.1760C>G	c.(1759-1761)aCc>aGc	p.T587S		NM_003399	NP_003390	O43895	XPP2_HUMAN	Homo sapiens X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound (XPNPEP2), mRNA.	587					cellular process|proteolysis	anchored to membrane|plasma membrane	aminopeptidase activity|metal ion binding|metalloexopeptidase activity			endometrium(3)|kidney(3)|large_intestine(5)|liver(1)|lung(20)|prostate(1)|skin(1)|upper_aerodigestive_tract(3)	37						AGCTACCTGACCTTTGAAGTG	0.567000													54	17					0	0	1	0	0
KCNA3	3738	broad.mit.edu	37	1	111217282	111217282	+	Silent	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr1:111217282C>T	uc001dzv.1	-	0	374	c.150G>A	c.(148-150)ccG>ccA	p.P50P		NM_002232	NP_002223	P22001	KCNA3_HUMAN	Homo sapiens potassium voltage-gated channel, shaker-related subfamily, member 3 (KCNA3), mRNA.	50						voltage-gated potassium channel complex	delayed rectifier potassium channel activity			endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(13)|lung(7)|ovary(4)|pancreas(1)|prostate(3)|skin(1)	38		all_cancers(81;3.92e-06)|all_epithelial(167;1.28e-05)|all_lung(203;0.000199)|Lung NSC(277;0.000398)		Lung(183;0.0235)|Colorectal(144;0.0306)|all cancers(265;0.0752)|Epithelial(280;0.0821)|COAD - Colon adenocarcinoma(174;0.132)|LUSC - Lung squamous cell carcinoma(189;0.133)		TCATGTCGGGCGGCAGCTCGC	0.776000													5	17					0	0	1	0	0
CPEB3	22849	broad.mit.edu	37	10	93999747	93999747	+	Missense_Mutation	SNP	C	C	G			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr10:93999747C>G	uc001khw.2	-	1	565	c.361G>C	c.(361-363)Gac>Cac	p.D121H	CPEB3_uc001khu.2_Missense_Mutation_p.D121H|CPEB3_uc001khv.2_Missense_Mutation_p.D121H|CPEB3_uc010qnn.2_Missense_Mutation_p.D121H	NM_014912	NP_055727	Q8NE35	CPEB3_HUMAN	Homo sapiens cytoplasmic polyadenylation element binding protein 3 (CPEB3), transcript variant 1, mRNA.	121	Pro-rich.						RNA binding|nucleotide binding			breast(1)|haematopoietic_and_lymphoid_tissue(2)|kidney(1)|large_intestine(5)|lung(5)|skin(2)|upper_aerodigestive_tract(2)	18		Colorectal(252;0.0869)				AAGAAGCTGTCCTCTACCGCG	0.667000													5	7					0	0	1	0	0
PARP4	143	broad.mit.edu	37	13	25044068	25044068	+	Silent	SNP	G	G	A	rs146166448	by1000genomes	TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr13:25044068G>A	uc001upl.3	-	15	2116	c.2010C>T	c.(2008-2010)ttC>ttT	p.F670F	PARP4_uc010tdc.2_Silent_p.F670F	NM_006437	NP_006428	Q9UKK3	PARP4_HUMAN	Homo sapiens poly (ADP-ribose) polymerase family, member 4 (PARP4), mRNA.	670	VIT.				DNA repair|cell death|inflammatory response|protein ADP-ribosylation|response to drug|transport	cytoplasm|nucleus|ribonucleoprotein complex|spindle microtubule	DNA binding|NAD+ ADP-ribosyltransferase activity|enzyme binding			autonomic_ganglia(1)|breast(3)|central_nervous_system(1)|endometrium(5)|kidney(3)|large_intestine(14)|lung(18)|ovary(3)|prostate(2)|skin(6)|stomach(3)|upper_aerodigestive_tract(3)|urinary_tract(1)	63		all_epithelial(30;7.67e-16)|Lung SC(185;0.0225)|Breast(139;0.052)		all cancers(112;0.000127)|Epithelial(112;0.000778)|Kidney(163;0.039)|OV - Ovarian serous cystadenocarcinoma(117;0.0578)|KIRC - Kidney renal clear cell carcinoma(186;0.135)|Lung(94;0.195)		TGAAGGCTTCGAAGCCACACA	0.458000													3	19					0	0	1	0	0
LOC220729	220729	broad.mit.edu	37	3	197348634	197348634	+	RNA	SNP	G	G	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr3:197348634G>C	uc011bug.2	-	3		c.457C>G			LOC220729_uc003fxy.3_Non-coding_Transcript|LOC220729_uc010iao.2_Intron					Homo sapiens succinate dehydrogenase complex, subunit A, flavoprotein (Fp) pseudogene (LOC220729), non-coding RNA.																		CAGCAGCACCGATGGGCCTGC	0.542000													5	87					0	0	1	0	0
SPDYE3	441272	broad.mit.edu	37	7	99909507	99909507	+	Silent	SNP	C	C	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr7:99909507C>T	uc022aij.1	+	3	863	c.679C>T	c.(679-681)Ctg>Ttg	p.L227L		NM_001004351	NP_001004351	A6NKU9	SPDE3_HUMAN	Homo sapiens speedy homolog E3 (Xenopus laevis) (SPDYE3), mRNA.	227										endometrium(10)|kidney(1)|lung(8)|urinary_tract(1)	20						GGCAGAGACGCTGTGTGGCCT	0.587000													40	80					0	0	1	0	0
ING3	54556	broad.mit.edu	37	7	120590817	120590817	+	Splice_Site	SNP	T	T	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr7:120590817T>C	uc003vjn.3	+	1	1	c.-133_splice	c.e1-1		ING3_uc011knr.1_Splice_Site|ING3_uc003vjl.3_Splice_Site|ING3_uc003vjm.1_Splice_Site|ING3_uc003vjo.3_Splice_Site|ING3_uc003vjp.3_Splice_Site|ING3_uc011kns.2_5'Flank	NM_019071	NP_061944	Q9NXR8	ING3_HUMAN	Homo sapiens inhibitor of growth family, member 3 (ING3), transcript variant 1, mRNA.						histone H2A acetylation|histone H4 acetylation|positive regulation of apoptosis|regulation of growth|regulation of transcription, DNA-dependent|transcription, DNA-dependent	NuA4 histone acetyltransferase complex|Piccolo NuA4 histone acetyltransferase complex	zinc ion binding			NS(1)|large_intestine(2)|lung(7)|ovary(1)|urinary_tract(1)	12	all_neural(327;0.117)					tttttttttcttttttttttt	0.542000													4	5					0	0	1	0	0
BC019672	0	broad.mit.edu	37	17	20319816	20319816	+	RNA	SNP	T	T	C			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:20319816T>C	uc010vzg.1	+	1		c.187T>C			BC019672_uc002gwx.3_Non-coding_Transcript					Homo sapiens cDNA FLJ59693 complete cds, moderately similar to Ankyrin repeat domain-containing protein 26.																		CAAAGGAAAATGACAGGCCCT	0.507000													5	43					0	0	1	0	0
OR9Q1	219956	broad.mit.edu	37	11	57947006	57947006	+	Missense_Mutation	SNP	G	G	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr11:57947006G>T	uc021qjm.1	+	0	90	c.90G>T	c.(88-90)ttG>ttT	p.L30F	OR9Q1_uc001nmj.3_Missense_Mutation_p.L30F	NM_001005212	NP_001005212	Q8NGQ5	OR9Q1_HUMAN	Homo sapiens olfactory receptor, family 9, subfamily Q, member 1 (OR9Q1), mRNA.	30					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			cervix(1)|endometrium(3)|kidney(1)|large_intestine(1)|liver(1)|lung(12)|ovary(1)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(2)	26		Breast(21;0.222)				TCTTCCTCTTGTTTTTATTTA	0.448000													4	144					0	0	1	0	0
PTEN	5728	broad.mit.edu	37	10	89717715	89717716	+	Frame_Shift_Ins	INS	-	-	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr10:89717715_89717716insA	uc001kfb.3	+	6	1772_1773	c.740_741insA	c.(739-741)ttafs	p.L247fs	PTEN_uc021pvw.1_Non-coding_Transcript	NM_000314	NP_000305	P60484	PTEN_HUMAN	Homo sapiens phosphatase and tensin homolog (PTEN), mRNA.	247	C2 tensin-type.				T cell receptor signaling pathway|activation of mitotic anaphase-promoting complex activity|apoptosis|canonical Wnt receptor signaling pathway|cell proliferation|central nervous system development|induction of apoptosis|inositol phosphate dephosphorylation|negative regulation of G1/S transition of mitotic cell cycle|negative regulation of cell migration|negative regulation of cyclin-dependent protein kinase activity involved in G1/S|negative regulation of focal adhesion assembly|negative regulation of protein kinase B signaling cascade|negative regulation of protein phosphorylation|nerve growth factor receptor signaling pathway|phosphatidylinositol dephosphorylation|phosphatidylinositol-mediated signaling|positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process|positive regulation of sequence-specific DNA binding transcription factor activity|protein stabilization|regulation of neuron projection development	PML body|cytosol|internal side of plasma membrane	PDZ domain binding|anaphase-promoting complex binding|enzyme binding|inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity|lipid binding|magnesium ion binding|phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase activity|phosphatidylinositol-3,4-bisphosphate 3-phosphatase activity|phosphatidylinositol-3-phosphatase activity|protein serine/threonine phosphatase activity|protein tyrosine phosphatase activity|protein tyrosine/serine/threonine phosphatase activity	p.0?(37)|p.P248fs*5(13)|p.P246L(8)|p.R55fs*1(5)|p.L247*(5)|p.P246fs*10(3)|p.P246fs*3(2)|p.L247F(2)|p.P246fs*11(2)|p.L247fs*10(2)|p.N212fs*1(2)|p.L247fs*6(2)|p.L247fs*4(2)|p.L247fs*5(2)|p.Y27fs*1(2)|p.P246fs*9(1)|p.P246fs*14(1)|p.P246fs*12(1)|p.L247L(1)|p.L247fs*11(1)|p.L247fs*12(1)|p.?(1)|p.P246_L247insGP(1)|p.G165_K342del(1)|p.L247fs*8(1)|p.G165_*404del(1)		NS(28)|autonomic_ganglia(2)|biliary_tract(6)|bone(5)|breast(92)|central_nervous_system(676)|cervix(26)|endometrium(1068)|eye(8)|haematopoietic_and_lymphoid_tissue(137)|kidney(24)|large_intestine(98)|liver(20)|lung(91)|meninges(2)|oesophagus(2)|ovary(82)|pancreas(6)|prostate(129)|salivary_gland(5)|skin(127)|soft_tissue(19)|stomach(30)|testis(1)|thyroid(29)|upper_aerodigestive_tract(29)|urinary_tract(12)|vulva(17)	2771		all_cancers(4;3.61e-31)|all_epithelial(4;3.96e-23)|Prostate(4;8.12e-23)|Breast(4;0.000111)|Melanoma(5;0.00146)|all_hematologic(4;0.00227)|Colorectal(252;0.00494)|all_neural(4;0.00513)|Acute lymphoblastic leukemia(4;0.0116)|Glioma(4;0.0274)|all_lung(38;0.132)	KIRC - Kidney renal clear cell carcinoma(1;0.214)	UCEC - Uterine corpus endometrioid carcinoma (6;0.000228)|all cancers(1;4.16e-84)|GBM - Glioblastoma multiforme(1;7.77e-49)|Epithelial(1;7.67e-41)|OV - Ovarian serous cystadenocarcinoma(1;6.22e-15)|BRCA - Breast invasive adenocarcinoma(1;1.1e-06)|Lung(2;3.18e-06)|Colorectal(12;4.88e-06)|LUSC - Lung squamous cell carcinoma(2;4.97e-06)|COAD - Colon adenocarcinoma(12;1.13e-05)|Kidney(1;0.000288)|KIRC - Kidney renal clear cell carcinoma(1;0.00037)|STAD - Stomach adenocarcinoma(243;0.218)		CCTCAGCCGTTACCTGTGTGTG	0.406		31	"""D, Mis, N, F, S"""		"""glioma,  prostate, endometrial"""	"""harmartoma, glioma,  prostate, endometrial"""			Proteus syndrome;Juvenile Polyposis;Hereditary Mixed Polyposis Syndrome type 1;Cowden syndrome;Bannayan-Riley-Ruvalcaba syndrome	HNSCC(9;0.0022)|TCGA GBM(2;<1E-08)|TSP Lung(26;0.18)			16	14	---	---	---	---					
HNRNPKP3	399881	broad.mit.edu	37	11	43283605	43283606	+	RNA	INS	-	-	A			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr11:43283605_43283606insA	uc001mxe.1	-	1		c.1330_1331insT								Homo sapiens heterogeneous nuclear ribonucleoprotein K pseudogene 3 (HNRNPKP3), non-coding RNA.																		GAAGCAAATGTAAAAAAAAAAA	0.386													2	4	---	---	---	---					
ZNF268	10795	broad.mit.edu	37	12	133780636	133780636	+	Frame_Shift_Del	DEL	T	T	-			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr12:133780636delT	uc010tch.2	+	5	2570	c.2364delT	c.(2362-2364)gctfs	p.A788fs	ZNF268_uc010tbv.1_Frame_Shift_Del_p.A627fs|ZNF268_uc010tbz.1_Frame_Shift_Del_p.A627fs|ZNF268_uc010tcc.1_Frame_Shift_Del_p.A627fs|ZNF268_uc010tcd.1_Frame_Shift_Del_p.A627fs|ZNF268_uc010tbx.2_3'UTR|ZNF268_uc010tbw.2_3'UTR|ZNF268_uc010tce.2_3'UTR|ZNF268_uc010tcg.2_3'UTR|ZNF268_uc010tca.2_3'UTR|ZNF268_uc010tcf.2_Frame_Shift_Del_p.A788fs|ZNF268_uc010tcb.2_3'UTR|ZNF268_uc021rgu.1_Frame_Shift_Del_p.A705fs	NM_001165881	NP_001159354	Q14587	ZN268_HUMAN	Homo sapiens zinc finger protein 268 (ZNF268), transcript variant 2, mRNA.	788						nucleus	DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			NS(2)|breast(3)|endometrium(4)|kidney(2)|large_intestine(2)|liver(2)|lung(7)|ovary(1)|skin(1)	24	all_neural(191;0.0982)|Medulloblastoma(191;0.163)	all_cancers(7;0.000215)|all_epithelial(31;0.096)		OV - Ovarian serous cystadenocarcinoma(86;3.58e-08)|Epithelial(86;6.6e-07)|all cancers(50;2.28e-05)		GTGGGAAAGCTTTTAGCAGCA	0.408													2	4	---	---	---	---					
TBCD	6904	broad.mit.edu	37	17	80900326	80900327	+	Frame_Shift_Ins	INS	-	-	T			TCGA-KK-A6E7-01A-11D-A31L-08	TCGA-KK-A6E7-11A-11D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6bde582d-6c64-4529-9771-e7f9df342b04	8a82ccc3-d5f6-4647-9699-604814692936	g.chr17:80900326_80900327insT	uc002kfz.3	+	38	3696_3697	c.3566_3567insT	c.(3565-3567)cctfs	p.P1189fs	TBCD_uc002kgd.3_Frame_Shift_Ins_p.P181fs|B3GNTL1_uc002kge.1_Non-coding_Transcript	NM_005993	NP_005984	Q9BTW9	TBCD_HUMAN	Homo sapiens tubulin folding cofactor D (TBCD), mRNA.	1189					'de novo' posttranslational protein folding|adherens junction assembly|negative regulation of cell-substrate adhesion|negative regulation of microtubule polymerization|post-chaperonin tubulin folding pathway|tight junction assembly	adherens junction|cytoplasm|lateral plasma membrane|microtubule|tight junction	GTPase activator activity|beta-tubulin binding|chaperone binding					Breast(20;0.000523)|all_neural(118;0.0779)	all_cancers(8;0.0266)|all_epithelial(8;0.0696)	OV - Ovarian serous cystadenocarcinoma(97;0.0868)|BRCA - Breast invasive adenocarcinoma(99;0.18)			CTTCTTCAGCCTGGTGCCTGCT	0.619													31	46	---	---	---	---					
