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
TCRA	0	broad.mit.edu	37	14	22964913	22964913	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr14:22964913C>T	uc001weq.3	+	0	18	c.4C>T	c.(4-6)Cgc>Tgc	p.R2C	TCRA_uc001wbw.2_Intron|TCRA_uc001wco.3_Intron|TCRA_uc010aje.1_Intron|TCRA_uc001wcp.2_Intron|TCRA_uc001wcr.1_Intron|TCRA_uc001wcs.1_Intron|TCRA_uc010ajf.1_Intron|TCRA_uc001wcx.4_Intron|TCRA_uc021rpr.1_Intron|TCRA_uc010ajj.1_Intron|TCRA_uc001wde.1_Intron|TCRA_uc010ajk.2_Intron|TCRA_uc001wdg.1_Intron|TCRA_uc021rpt.1_Intron|TCRA_uc010ajl.1_Intron|AV4S1_uc021rpv.1_Intron|TCRA_uc010ajo.1_Intron|TCRA_uc010ajp.1_Intron|TCRA_uc021rpw.1_Intron|TCRA_uc001wdv.4_Intron|TCRA_uc001wec.3_Intron|TCRA_uc001wee.4_Intron|TCRA_uc010tmt.1_Intron|TCRA_uc010ajv.1_Intron|TCRA_uc001weg.2_Intron|TCRA_uc001weh.1_Intron|TCRA_uc001wei.3_Intron|TCRA_uc001wej.3_Intron|TCRA_uc001wek.3_Intron|TCRA_uc001wel.3_Intron|TCRA_uc001wem.4_Intron|TCRA_uc001wen.2_Intron|TCRA_uc001weo.2_Intron|TCRA_uc001wep.3_Intron|TCRA_uc021rpz.1_5'Flank|TCRA_uc021rqa.1_5'Flank|TCRA_uc021rqb.1_5'Flank|TCRA_uc001wet.3_5'Flank					SubName: Full=TRA@ protein;																		CAATGACATGCGCTTTGGAGC	0.498000													13	91					0	0	1	0	0
XKR4	114786	broad.mit.edu	37	8	56015725	56015725	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr8:56015725C>T	uc003xsf.3	+	0	709	c.677C>T	c.(676-678)gCg>gTg	p.A226V		NM_052898	NP_443130	Q5GH76	XKR4_HUMAN	Homo sapiens XK, Kell blood group complex subunit-related family, member 4 (XKR4), mRNA.	226						integral to membrane				NS(1)|autonomic_ganglia(1)|endometrium(1)|kidney(3)|large_intestine(4)|liver(2)|lung(12)|ovary(1)|pancreas(2)|prostate(2)|skin(3)|upper_aerodigestive_tract(2)	34			Epithelial(17;0.000117)|all cancers(17;0.000836)			AACATCGCCGCGGCCAACAGC	0.652000													4	85					0	0	1	0	0
ZNF831	128611	broad.mit.edu	37	20	57767498	57767498	+	Missense_Mutation	SNP	C	C	T	rs139591279		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr20:57767498C>T	uc002yan.3	+	0	1424	c.1424C>T	c.(1423-1425)aCg>aTg	p.T475M		NM_178457	NP_848552	Q5JPB2	ZN831_HUMAN	Homo sapiens zinc finger protein 831 (ZNF831), mRNA.	475						intracellular	nucleic acid binding|zinc ion binding	p.T475M(2)		NS(1)|breast(3)|central_nervous_system(1)|cervix(1)|endometrium(3)|kidney(2)|large_intestine(15)|lung(71)|ovary(2)|pancreas(1)|prostate(4)|skin(16)|upper_aerodigestive_tract(2)|urinary_tract(3)	125	all_lung(29;0.0085)					TCCACCTGGACGCCCCCAGAC	0.672000													13	96					0	0	1	0	0
EP300	2033	broad.mit.edu	37	22	41573200	41573200	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr22:41573200C>T	uc003azl.4	+	30	5880	c.5485C>T	c.(5485-5487)Cgc>Tgc	p.R1829C		NM_001429	NP_001420	Q09472	EP300_HUMAN	Homo sapiens E1A binding protein p300 (EP300), mRNA.	1829					DNA damage response, signal transduction by p53 class mediator resulting in induction of apoptosis|N-terminal peptidyl-lysine acetylation|apoptosis|cell cycle|histone H4 acetylation|interspecies interaction between organisms|positive regulation of sequence-specific DNA binding transcription factor activity|positive regulation of transcription from RNA polymerase II promoter|regulation of androgen receptor signaling pathway|response to estrogen stimulus|response to hypoxia	centrosome|histone acetyltransferase complex	DNA binding|RNA polymerase II activating transcription factor binding|androgen receptor binding|beta-catenin binding|histone acetyltransferase activity|transcription coactivator activity|zinc ion binding			NS(2)|breast(11)|central_nervous_system(7)|cervix(1)|endometrium(10)|haematopoietic_and_lymphoid_tissue(31)|kidney(5)|large_intestine(31)|liver(2)|lung(33)|ovary(2)|pancreas(4)|prostate(1)|skin(6)|stomach(1)|upper_aerodigestive_tract(8)|urinary_tract(16)	171						CCAAATGCTTCGCAGGAGGAT	0.607000			"""T,  N, F, Mis, O"""	"""MLL, RUNXBP2"""	"""colorectal, breast, pancreatic, AML, ALL, DLBCL"""				Rubinstein-Taybi syndrome				12	126					0	0	1	0	0
KLHL12	59349	broad.mit.edu	37	1	202861726	202861726	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:202861726C>T	uc001gyo.1	-	11	1842	c.1642G>A	c.(1642-1644)Gaa>Aaa	p.E548K	KLHL12_uc001gym.1_3'UTR|KLHL12_uc001gyn.1_3'UTR|KLHL12_uc010pqc.1_Missense_Mutation_p.E586K	NM_021633	NP_067646	Q53G59	KLH12_HUMAN	Homo sapiens kelch-like 12 (Drosophila) (KLHL12), mRNA.	548	Interaction with DVL3.				Wnt receptor signaling pathway		protein binding			NS(3)|breast(2)|endometrium(1)|large_intestine(1)|lung(6)|stomach(1)	14			BRCA - Breast invasive adenocarcinoma(75;0.166)			GTCACGACTTCCCAGCTGTCG	0.478000													9	79					0	0	1	0	0
SCARB1	949	broad.mit.edu	37	12	125299595	125299595	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr12:125299595C>T	uc001ugp.3	-	2	603	c.350G>A	c.(349-351)cGc>cAc	p.R117H	SCARB1_uc001ugm.4_Missense_Mutation_p.R117H|SCARB1_uc001ugn.4_Missense_Mutation_p.R117H|SCARB1_uc010tbd.2_Missense_Mutation_p.R117H|SCARB1_uc001ugo.4_Missense_Mutation_p.R117H	NM_001082959	NP_001076428	Q8WTV0	SCRB1_HUMAN	Homo sapiens scavenger receptor class B, member 1 (SCARB1), transcript variant 2, mRNA.	117					adhesion to symbiont|cell adhesion|cholesterol efflux|cholesterol homeostasis|cholesterol import|detection of lipopolysaccharide|high-density lipoprotein particle clearance|high-density lipoprotein particle remodeling|lipopolysaccharide transport|lipoprotein metabolic process|positive regulation of cholesterol storage|positive regulation of endothelial cell migration|positive regulation of nitric-oxide synthase activity|recognition of apoptotic cell|reverse cholesterol transport|triglyceride homeostasis|wound healing	caveola	1-phosphatidylinositol binding|apolipoprotein A-I binding|high-density lipoprotein particle receptor activity|lipopolysaccharide receptor activity|low-density lipoprotein particle binding|phosphatidylserine binding|transporter activity			endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(4)|lung(7)|prostate(1)	17	all_neural(191;0.101)|Medulloblastoma(191;0.163)			OV - Ovarian serous cystadenocarcinoma(86;0.000116)|Epithelial(86;0.000415)|all cancers(50;0.00395)	Phosphatidylserine(DB00144)	CTGGAAGGTGCGGTACTCGAG	0.612000													4	69					0	0	1	0	0
OR4D10	390197	broad.mit.edu	37	11	59245336	59245336	+	Missense_Mutation	SNP	C	C	G			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr11:59245336C>G	uc001nnz.1	+	0	434	c.434C>G	c.(433-435)aCa>aGa	p.T145R		NM_001004705	NP_001004705	Q8NGI6	OR4DA_HUMAN	Homo sapiens olfactory receptor, family 4, subfamily D, member 10 (OR4D10), mRNA.	145					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity	p.T145I(1)|p.T143I(1)		NS(1)|breast(2)|endometrium(2)|kidney(2)|large_intestine(4)|lung(12)|ovary(2)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	30						ATTGGGCTCACAGTGGCTGCC	0.517000													14	100					0	0	1	0	0
LMX1B	4010	broad.mit.edu	37	9	129458133	129458133	+	Missense_Mutation	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr9:129458133G>A	uc011maa.2	+	6	942	c.935G>A	c.(934-936)cGc>cAc	p.R312H	LMX1B_uc004bqi.3_Missense_Mutation_p.R301H|LMX1B_uc004bqj.3_Missense_Mutation_p.R301H	NM_001174146	NP_001167617	O60663	LMX1B_HUMAN	Homo sapiens LIM homeobox transcription factor 1, beta (LMX1B), transcript variant 3, mRNA.	278					dorsal/ventral pattern formation|in utero embryonic development	nucleus	protein binding|sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			endometrium(1)|large_intestine(3)|lung(9)|ovary(1)|skin(1)	15						CTGTCCAGCCGCATGGAGGGC	0.662000									Nail-Patella Syndrome				9	75					0	0	1	0	0
CKAP5	9793	broad.mit.edu	37	11	46801810	46801810	+	Silent	SNP	A	A	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr11:46801810A>C	uc001ndi.2	-	19	2493	c.2367T>G	c.(2365-2367)tcT>tcG	p.S789S	CKAP5_uc009ylg.1_Silent_p.S675S|CKAP5_uc001ndj.2_Silent_p.S789S|Metazoa_SRP_uc021qiq.1_5'Flank	NM_001008938	NP_001008938	Q14008	CKAP5_HUMAN	Homo sapiens cytoskeleton associated protein 5 (CKAP5), transcript variant 1, mRNA.	789					G2/M transition of mitotic cell cycle|RNA transport|cell division|centrosome organization|establishment or maintenance of microtubule cytoskeleton polarity|mitotic prometaphase|spindle organization	centrosome|cytosol	protein binding			breast(1)|cervix(3)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(7)|lung(13)|ovary(1)|prostate(1)|skin(4)|stomach(1)|upper_aerodigestive_tract(1)	43						ACATTCGCAAAGAGGGACCAA	0.423000													10	45					0	0	1	0	0
KLHL12	59349	broad.mit.edu	37	1	202861756	202861756	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:202861756C>T	uc001gyo.1	-	11	1812	c.1612G>A	c.(1612-1614)Gaa>Aaa	p.E538K	KLHL12_uc001gym.1_3'UTR|KLHL12_uc001gyn.1_3'UTR|KLHL12_uc010pqc.1_Missense_Mutation_p.E576K	NM_021633	NP_067646	Q53G59	KLH12_HUMAN	Homo sapiens kelch-like 12 (Drosophila) (KLHL12), mRNA.	538	Interaction with DVL3.				Wnt receptor signaling pathway		protein binding			NS(3)|breast(2)|endometrium(1)|large_intestine(1)|lung(6)|stomach(1)	14			BRCA - Breast invasive adenocarcinoma(75;0.166)			TCATAACATTCAATGCTACTT	0.483000													7	60					0	0	1	0	0
PNMA2	10687	broad.mit.edu	37	8	26366213	26366213	+	Nonsense_Mutation	SNP	G	G	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr8:26366213G>T	uc022atc.1	-	0	59	c.59C>A	c.(58-60)tCa>tAa	p.S20*	PNMA2_uc003xez.2_Nonsense_Mutation_p.S20*	NM_007257	NP_009188	Q9UL42	PNMA2_HUMAN	Homo sapiens paraneoplastic antigen MA2 (PNMA2), mRNA.	20					apoptosis	nucleolus	protein binding			NS(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(3)|lung(3)	11		all_cancers(63;0.109)|Ovarian(32;2.61e-05)|all_epithelial(46;0.105)		UCEC - Uterine corpus endometrioid carcinoma (27;0.0196)|Epithelial(17;3.13e-11)|Colorectal(74;0.123)		aaccatcagtgacttctgctc	0.512000													32	179					0	0	1	0	0
OAS2	4939	broad.mit.edu	37	12	113447043	113447043	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr12:113447043C>T	uc001tuj.3	+	9	2187	c.2047C>T	c.(2047-2049)Ccg>Tcg	p.P683S	OAS2_uc001tui.1_Missense_Mutation_p.P683S	NM_016817	NP_058197	P29728	OAS2_HUMAN	Homo sapiens 2'-5'-oligoadenylate synthetase 2, 69/71kDa (OAS2), transcript variant 1, mRNA.	683	OAS domain 2.				interferon-gamma-mediated signaling pathway|nucleobase, nucleoside, nucleotide and nucleic acid metabolic process|type I interferon-mediated signaling pathway	endoplasmic reticulum|membrane|microsome|mitochondrion|nucleus	ATP binding|RNA binding|nucleotidyltransferase activity			NS(1)|breast(2)|endometrium(4)|large_intestine(7)|lung(8)|ovary(1)|prostate(1)|skin(3)|upper_aerodigestive_tract(1)	28						TTGGAAAGTGCCGGTAAAAGT	0.458000													6	280					0	0	1	0	0
MEF2D	4209	broad.mit.edu	37	1	156446862	156446862	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:156446862C>T	uc001fpc.3	-	6	1187	c.797G>A	c.(796-798)cGc>cAc	p.R266H	MEF2D_uc001fpb.3_Missense_Mutation_p.R266H|MEF2D_uc001fpd.3_Missense_Mutation_p.R266H|MEF2D_uc009wsa.3_Non-coding_Transcript|MEF2D_uc001fpe.1_Missense_Mutation_p.R266H	NM_005920	NP_005911	Q14814	MEF2D_HUMAN	Homo sapiens myocyte enhancer factor 2D (MEF2D), mRNA.	266					apoptosis|muscle organ development|nervous system development|positive regulation of transcription from RNA polymerase II promoter	nucleus	RNA polymerase II regulatory region sequence-specific DNA binding|activating transcription factor binding|histone deacetylase binding|sequence-specific DNA binding RNA polymerase II transcription factor activity			endometrium(4)|kidney(1)|large_intestine(2)|lung(6)|ovary(1)|urinary_tract(1)	15	all_hematologic(923;0.088)|Hepatocellular(266;0.158)					GTCGGGCTTGCGGCTGGGGGC	0.617000													4	153					0	0	1	0	0
HELB	92797	broad.mit.edu	37	12	66725028	66725028	+	Missense_Mutation	SNP	G	G	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr12:66725028G>T	uc001sti.2	+	11	2793	c.2765G>T	c.(2764-2766)cGa>cTa	p.R922L	HELB_uc010ssz.1_Non-coding_Transcript|HELB_uc009zqt.1_Non-coding_Transcript	NM_033647	NP_387467	Q8NG08	HELB_HUMAN	Homo sapiens helicase (DNA) B (HELB), mRNA.	922					DNA replication, synthesis of RNA primer		ATP binding|ATP-dependent 5'-3' DNA helicase activity|single-stranded DNA-dependent ATP-dependent DNA helicase activity			autonomic_ganglia(1)|breast(2)|central_nervous_system(1)|cervix(1)|endometrium(3)|kidney(2)|large_intestine(10)|lung(15)|pancreas(1)|prostate(3)|upper_aerodigestive_tract(1)	40			GBM - Glioblastoma multiforme(2;0.000142)	GBM - Glioblastoma multiforme(28;0.0265)		GGCCGCTGCCGAGTGTATGTG	0.532000													4	76					0	0	1	0	0
TAF5L	27097	broad.mit.edu	37	1	229738251	229738251	+	Silent	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:229738251G>A	uc001htq.3	-	3	829	c.663C>T	c.(661-663)aaC>aaT	p.N221N	TAF5L_uc001htr.3_Silent_p.N221N	NM_014409	NP_055224	O75529	TAF5L_HUMAN	Homo sapiens TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, 65kDa (TAF5L), transcript variant 1, mRNA.	221					histone H3 acetylation|transcription from RNA polymerase II promoter	STAGA complex|transcription factor TFTC complex	sequence-specific DNA binding transcription factor activity|transcription coactivator activity			breast(2)|central_nervous_system(1)|endometrium(1)|kidney(2)|lung(4)|ovary(1)	11	Breast(184;0.193)|Ovarian(103;0.249)	Prostate(94;0.167)				GCTCCAAACCGTTGTTCTCAC	0.552000													4	104					0	0	1	0	0
EHBP1	23301	broad.mit.edu	37	2	63101583	63101583	+	Silent	SNP	G	G	A	rs148159032		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr2:63101583G>A	uc002sby.3	+	10	1688	c.1206G>A	c.(1204-1206)ccG>ccA	p.P402P	EHBP1_uc010fcp.3_Silent_p.P367P|EHBP1_uc002sbz.3_Silent_p.P367P|EHBP1_uc002scb.3_Silent_p.P367P	NM_015252	NP_056067	Q8NDI1	EHBP1_HUMAN	Homo sapiens EH domain binding protein 1 (EHBP1), transcript variant 1, mRNA.	402						cytoplasm|membrane		p.P402Q(1)		biliary_tract(1)|breast(3)|cervix(1)|endometrium(4)|kidney(4)|large_intestine(8)|lung(22)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	47	Lung NSC(7;0.0951)|all_lung(7;0.169)		LUSC - Lung squamous cell carcinoma(7;7.74e-05)|Epithelial(17;0.189)			GAAAGGCCCCGGCTCCACCAG	0.388000													19	121					0	0	1	0	0
FLJ43315	644316	broad.mit.edu	37	GL000211.1	107462	107462	+	RNA	SNP	A	A	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chrGL000211.1:107462A>T	uc003boa.3	+	4		c.1002A>T								Homo sapiens asparagine synthetase pseudogene (FLJ43315), non-coding RNA.																		GTAAGGGTCAATTTTTTATAT	0.294000													6	85					0	0	1	0	0
DCAF8	50717	broad.mit.edu	37	1	160187426	160187426	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:160187426C>T	uc001fvo.2	-	13	2062	c.1750G>A	c.(1750-1752)Gac>Aac	p.D584N	DCAF8_uc001fvn.2_Missense_Mutation_p.D584N|DCAF8_uc009wth.2_Missense_Mutation_p.D584N|DCAF8_uc010pjb.1_Missense_Mutation_p.D584N|DCAF8_uc010pjc.1_Missense_Mutation_p.D738N	NM_015726	NP_056541	Q5TAQ9	DCAF8_HUMAN	Homo sapiens DDB1 and CUL4 associated factor 8 (DCAF8), transcript variant 1, mRNA.	584						CUL4 RING ubiquitin ligase complex	protein binding			cervix(1)|endometrium(4)|kidney(2)|large_intestine(6)|lung(16)|skin(3)|upper_aerodigestive_tract(1)	33						TCCTCCTCGTCCGATGTGTCT	0.622000													7	72					0	0	1	0	0
CACNA1A	773	broad.mit.edu	37	19	13616783	13616783	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr19:13616783C>T	uc002mwy.3	-	0	492	c.256G>A	c.(256-258)Gtg>Atg	p.V86M	CACNA1A_uc010xnd.2_Missense_Mutation_p.V86M|CACNA1A_uc021ups.1_Missense_Mutation_p.V86M|CACNA1A_uc010xne.2_Missense_Mutation_p.V86M|CACNA1A_uc010dze.2_Missense_Mutation_p.V86M|CACNA1A_uc021upt.1_Missense_Mutation_p.V86M	NM_001127222	NP_001120694	O00555	CAC1A_HUMAN	Homo sapiens calcium channel, voltage-dependent, P/Q type, alpha 1A subunit (CACNA1A), transcript variant 4, mRNA.	86					cell death|elevation of cytosolic calcium ion concentration|energy reserve metabolic process|membrane depolarization|regulation of insulin secretion	cytoplasm|nucleus	syntaxin binding			breast(2)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(3)|lung(25)|prostate(2)|urinary_tract(1)	42			OV - Ovarian serous cystadenocarcinoma(19;5.07e-21)		Bepridil(DB01244)|Cinnarizine(DB00568)|Loperamide(DB00836)|Nisoldipine(DB00401)|Pregabalin(DB00230)	TTTCTCACCACGTTGTCTTCG	0.597000													9	36					0	0	1	0	0
MCC	4163	broad.mit.edu	37	5	112824048	112824048	+	Missense_Mutation	SNP	T	T	C	rs35336557		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr5:112824048T>C	uc003kql.4	-	0	480	c.64A>G	c.(64-66)Agc>Ggc	p.S22G		NM_001085377	NP_001078846	P23508	CRCM_HUMAN	Homo sapiens mutated in colorectal cancers (MCC), transcript variant 1, mRNA.	550					Wnt receptor signaling pathway|negative regulation of canonical Wnt receptor signaling pathway|negative regulation of epithelial cell migration|negative regulation of epithelial cell proliferation	cytoplasm|nucleus|plasma membrane	protein binding|receptor activity	p.S22*(1)		endometrium(4)|kidney(3)|large_intestine(15)|liver(2)|lung(8)|ovary(2)|pancreas(1)|prostate(4)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	42		all_cancers(142;5.89e-08)|all_epithelial(76;3.57e-11)|all_lung(232;0.000605)|Lung NSC(810;0.000697)|Colorectal(10;0.00146)|Prostate(80;0.00174)|Ovarian(225;0.0175)|Breast(839;0.198)		OV - Ovarian serous cystadenocarcinoma(64;2.04e-54)|Epithelial(69;9.69e-49)|all cancers(49;6.25e-44)|COAD - Colon adenocarcinoma(37;0.0432)|Colorectal(14;0.0766)		ctgctgccgctgccgccgccg	0.736000													4	29					0	0	1	0	0
GPR98	84059	broad.mit.edu	37	5	90083965	90083965	+	Silent	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr5:90083965C>T	uc003kju.3	+	67	13827	c.13731C>T	c.(13729-13731)agC>agT	p.S4577S	GPR98_uc003kjt.3_Silent_p.S2283S|GPR98_uc003kjw.3_Silent_p.S238S	NM_032119	NP_115495	Q8WXG9	GPR98_HUMAN	Homo sapiens G protein-coupled receptor 98 (GPR98), transcript variant 1, mRNA.	4577	Calx-beta 31.				cell communication|cell-cell adhesion|maintenance of organ identity|neuropeptide signaling pathway|photoreceptor cell maintenance	cell surface|cytoplasm|integral to membrane|plasma membrane	G-protein coupled receptor activity|calcium ion binding			NS(4)|breast(7)|central_nervous_system(6)|cervix(1)|endometrium(13)|haematopoietic_and_lymphoid_tissue(3)|kidney(18)|large_intestine(46)|liver(2)|lung(80)|ovary(12)|pancreas(5)|prostate(1)|skin(50)|stomach(7)|upper_aerodigestive_tract(8)|urinary_tract(6)	269		all_cancers(142;1.05e-09)|all_epithelial(76;1.81e-12)|all_lung(232;5.41e-06)|Lung NSC(167;1.72e-05)|Ovarian(174;0.00948)|Colorectal(57;0.133)|Breast(839;0.192)		OV - Ovarian serous cystadenocarcinoma(54;7.01e-30)|Epithelial(54;6.79e-25)|all cancers(79;1.88e-20)		ACCCAGTGAGCGGGTTGTTCT	0.433000													4	61					0	0	1	0	0
ADAMTS5	11096	broad.mit.edu	37	21	28327086	28327086	+	Silent	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr21:28327086G>A	uc002ymg.3	-	1	1938	c.1209C>T	c.(1207-1209)caC>caT	p.H403H		NM_007038	NP_008969	Q9UNA0	ATS5_HUMAN	Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif, 5 (ADAMTS5), mRNA.	403	Peptidase M12B.				proteolysis	proteinaceous extracellular matrix	integrin binding|metalloendopeptidase activity|zinc ion binding	p.H403H(2)		breast(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(17)|lung(34)|ovary(3)|pancreas(1)|prostate(1)|skin(3)|upper_aerodigestive_tract(3)	72						TGAAGGCTGCGTGGAGGCCAT	0.498000													13	78					0	0	1	0	0
TTC12	54970	broad.mit.edu	37	11	113196336	113196336	+	Missense_Mutation	SNP	A	A	G			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr11:113196336A>G	uc001pnv.3	+	5	518	c.413A>G	c.(412-414)gAc>gGc	p.D138G	TTC12_uc001pnu.3_Missense_Mutation_p.D138G|TTC12_uc001pnw.3_Non-coding_Transcript|TTC12_uc001pnx.3_5'UTR	NM_017868	NP_060338	Q9H892	TTC12_HUMAN	Homo sapiens tetratricopeptide repeat domain 12 (TTC12), mRNA.	138							binding	p.K137N(1)		breast(1)|central_nervous_system(1)|cervix(1)|endometrium(2)|kidney(1)|large_intestine(6)|lung(12)|pancreas(2)|skin(3)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	32		all_cancers(61;2.73e-16)|all_epithelial(67;8.64e-10)|Melanoma(852;1.46e-05)|all_hematologic(158;0.00014)|Acute lymphoblastic leukemia(157;0.000967)|Breast(348;0.0101)|all_neural(223;0.0281)|Medulloblastoma(222;0.0425)|Prostate(24;0.183)|Renal(330;0.187)		BRCA - Breast invasive adenocarcinoma(274;5.3e-06)|Epithelial(105;8.37e-05)|all cancers(92;0.000694)		AAGCTGAAGGACATGAAAGTG	0.468000													19	98					0	0	1	0	0
DAPK1	1612	broad.mit.edu	37	9	90321394	90321394	+	Missense_Mutation	SNP	C	C	G			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr9:90321394C>G	uc004apc.3	+	25	3546	c.3408C>G	c.(3406-3408)caC>caG	p.H1136Q	DAPK1_uc004apd.3_Missense_Mutation_p.H1136Q|DAPK1_uc011ltg.2_Missense_Mutation_p.H1070Q|DAPK1_uc011lth.2_Missense_Mutation_p.H873Q|DAPK1_uc004apg.2_Missense_Mutation_p.H113Q	NM_004938	NP_004929	P53355	DAPK1_HUMAN	Homo sapiens death-associated protein kinase 1 (DAPK1), mRNA.	1136					apoptosis|induction of apoptosis by extracellular signals|intracellular protein kinase cascade	actin cytoskeleton|cytoplasm	ATP binding|calmodulin binding|protein serine/threonine kinase activity			breast(5)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(27)|liver(2)|lung(17)|ovary(1)|prostate(2)|skin(3)|stomach(1)	72						CCGTGGAACACCTCACCCCCT	0.612000									Chronic Lymphocytic Leukemia, Familial Clustering of				3	47					0	0	1	0	0
BOD1L1	259282	broad.mit.edu	37	4	13601210	13601210	+	Silent	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr4:13601210G>A	uc003gmz.1	-	9	7431	c.7314C>T	c.(7312-7314)tgC>tgT	p.C2438C	BOD1L1_uc010idr.1_Silent_p.C1775C	NM_148894	NP_683692	Q8NFC6	BOD1L_HUMAN	Homo sapiens biorientation of chromosomes in cell division 1-like (BOD1L), mRNA.	2438							DNA binding										CTATTTCGGGGCACTCCTTGC	0.498000											OREG0016115	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)	4	164					0	0	1	0	0
ANKRD20A9P	284232	broad.mit.edu	37	13	19413025	19413025	+	RNA	SNP	A	A	G			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr13:19413025A>G	uc010tcj.1	-	0		c.33085T>C								Homo sapiens ankyrin repeat domain 20 family, member A9, pseudogene (ANKRD20A9P), non-coding RNA.																		AATAACCTGCACATCCATGCA	0.299000													3	24					0	0	1	0	0
AL117485	0	broad.mit.edu	37	22	18844763	18844763	+	RNA	SNP	T	T	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr22:18844763T>C	uc002zoe.3	+	3		c.2017T>C			AL117485_uc002zof.3_5'Flank					Homo sapiens cDNA FLJ76361 complete cds.																		TCACAGCCTCTGAGGGCAGCA	0.562000													12	18					0	0	1	0	0
ANKRD20A9P	284232	broad.mit.edu	37	13	19413033	19413033	+	RNA	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr13:19413033G>A	uc010tcj.1	-	0		c.33077C>T								Homo sapiens ankyrin repeat domain 20 family, member A9, pseudogene (ANKRD20A9P), non-coding RNA.																		GCACATCCATGCACTAAAAAG	0.294000													3	23					0	0	1	0	0
DDX11	1663	broad.mit.edu	37	12	31237922	31237922	+	Missense_Mutation	SNP	G	G	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr12:31237922G>C	uc001rjt.1	+	4	751	c.500G>C	c.(499-501)aGa>aCa	p.R167T	DDX11_uc010sjw.1_Missense_Mutation_p.R167T|DDX11_uc010sjx.1_Non-coding_Transcript|DDX11_uc001rjr.1_Missense_Mutation_p.R167T|DDX11_uc001rjs.1_Missense_Mutation_p.R167T|DDX11_uc001rju.1_5'UTR|DDX11_uc001rjv.1_Missense_Mutation_p.R167T|DDX11_uc001rjw.1_Missense_Mutation_p.R141T|DDX11_uc001rjx.1_5'Flank	NM_152438	NP_689651	Q96FC9	DDX11_HUMAN	Homo sapiens DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 (DDX11), transcript variant 3, mRNA.	167	Glu-rich.|Helicase ATP-binding.				G2/M transition of mitotic cell cycle|S phase of mitotic cell cycle|interspecies interaction between organisms|mitotic sister chromatid segregation|positive regulation of cell proliferation|sister chromatid cohesion	midbody|nuclear chromatin|nucleolus|spindle pole	ATP binding|ATP-dependent DNA helicase activity|DNA binding|RNA binding|protein binding	p.R167T(18)		breast(4)|central_nervous_system(1)|cervix(1)|endometrium(4)|kidney(11)|large_intestine(5)|lung(23)|prostate(3)|skin(2)|stomach(1)|upper_aerodigestive_tract(2)	57	all_cancers(9;1.77e-11)|all_lung(12;6.21e-11)|all_epithelial(9;6.49e-11)|Lung NSC(12;1.06e-08)|Acute lymphoblastic leukemia(23;0.0122)|all_hematologic(23;0.0429)|Lung SC(12;0.0592)|Esophageal squamous(101;0.233)					GAAGAAGAAAGAGAGAATCTC	0.612000										Multiple Myeloma(12;0.14)			3	27					0	0	1	0	0
LOC100286793	100286793	broad.mit.edu	37	1	143744418	143744418	+	RNA	SNP	C	C	T	rs71661951		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:143744418C>T	uc001ejp.3	-	0		c.170G>A			LOC100286793_uc001ejr.4_Non-coding_Transcript|LOC100286793_uc009whx.2_Non-coding_Transcript|LOC100286793_uc009why.2_Non-coding_Transcript					Homo sapiens uncharacterized LOC100286793 (LOC100286793), non-coding RNA.																		CAAGTGGTTTCGGAAGTGATC	0.567000													6	17					0	0	1	0	0
MLL3	58508	broad.mit.edu	37	7	151878166	151878166	+	Missense_Mutation	SNP	G	G	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr7:151878166G>C	uc003wla.3	-	35	6998	c.6779C>G	c.(6778-6780)gCt>gGt	p.A2260G	MLL3_uc003wkz.3_Missense_Mutation_p.A1321G	NM_170606	NP_733751	Q8NEZ4	MLL3_HUMAN	Homo sapiens myeloid/lymphoid or mixed-lineage leukemia 3 (MLL3), mRNA.	2260	Pro-rich.				intracellular signal transduction|regulation of transcription, DNA-dependent|transcription, DNA-dependent		DNA binding|protein binding|zinc ion binding			NS(6)|biliary_tract(9)|breast(24)|central_nervous_system(18)|cervix(6)|endometrium(31)|haematopoietic_and_lymphoid_tissue(1)|kidney(26)|large_intestine(52)|liver(1)|lung(102)|ovary(10)|pancreas(17)|prostate(15)|skin(20)|soft_tissue(1)|stomach(3)|upper_aerodigestive_tract(8)|urinary_tract(15)	365	all_neural(206;0.187)	all_hematologic(28;0.0592)|Prostate(32;0.0906)	OV - Ovarian serous cystadenocarcinoma(82;0.00715)	UCEC - Uterine corpus endometrioid carcinoma (81;0.0597)|BRCA - Breast invasive adenocarcinoma(188;0.0462)		GCCAGGTAAAGCTGGTCCTCG	0.517000			N		medulloblastoma								19	81					0	0	1	0	0
ADCY4	196883	broad.mit.edu	37	14	24793576	24793576	+	Silent	SNP	C	C	T	rs141339113		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr14:24793576C>T	uc001wow.3	-	14	2264	c.1845G>A	c.(1843-1845)acG>acA	p.T615T	ADCY4_uc010toh.2_Silent_p.T301T|ADCY4_uc001wox.3_Silent_p.T615T|ADCY4_uc001woy.3_Silent_p.T615T	NM_001198568	NP_001185497	Q8NFM4	ADCY4_HUMAN	Homo sapiens adenylate cyclase 4 (ADCY4), transcript variant 3, mRNA.	615					activation of adenylate cyclase activity by G-protein signaling pathway|activation of phospholipase C activity|activation of protein kinase A activity|cellular response to glucagon stimulus|energy reserve metabolic process|inhibition of adenylate cyclase activity by G-protein signaling pathway|nerve growth factor receptor signaling pathway|synaptic transmission|transmembrane transport|water transport	cytoplasm|integral to membrane|plasma membrane	ATP binding|adenylate cyclase activity|metal ion binding|protein binding			cervix(1)|endometrium(1)|kidney(1)|large_intestine(10)|lung(13)|ovary(2)|pancreas(1)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1)	34				GBM - Glioblastoma multiforme(265;0.0192)		TGATGCTATACGTGATGGCCA	0.567000													10	87					0	0	1	0	0
AL117485	0	broad.mit.edu	37	22	18844888	18844888	+	RNA	SNP	A	A	G			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr22:18844888A>G	uc002zoe.3	+	3		c.2142A>G			AL117485_uc002zof.3_5'Flank					Homo sapiens cDNA FLJ76361 complete cds.																		GCTCACGGAAATACAGCTTCA	0.587000													10	117					0	0	1	0	0
NPEPPS	9520	broad.mit.edu	37	17	45668127	45668127	+	Nonsense_Mutation	SNP	G	G	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr17:45668127G>A	uc002ilr.4	+	9	1363	c.1140G>A	c.(1138-1140)tgG>tgA	p.W380*	NPEPPS_uc010wkt.2_Nonsense_Mutation_p.W376*|NPEPPS_uc010wku.2_Nonsense_Mutation_p.W344*|NPEPPS_uc010wkv.2_5'UTR	NM_006310	NP_006301	P55786	PSA_HUMAN	Homo sapiens aminopeptidase puromycin sensitive (NPEPPS), mRNA.	380					proteolysis	cytosol|nucleus	aminopeptidase activity|metallopeptidase activity|protein binding|zinc ion binding			breast(1)|central_nervous_system(1)|endometrium(7)|kidney(1)|large_intestine(6)|lung(7)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)	27						TTGCATCCTGGATTGAATATC	0.383000													7	61					0	0	1	0	0
THAP7	80764	broad.mit.edu	37	22	21354950	21354950	+	Silent	SNP	T	T	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr22:21354950T>C	uc002ztr.1	-	3	393	c.363A>G	c.(361-363)agA>agG	p.R121R	THAP7_uc002zts.1_Silent_p.R121R|THAP7-AS1_uc002ztt.1_5'Flank|THAP7-AS1_uc002ztv.3_5'Flank	NM_001008695	NP_085050	Q9BT49	THAP7_HUMAN	Homo sapiens THAP domain containing 7 (THAP7), transcript variant 2, mRNA.	121					negative regulation of transcription, DNA-dependent|transcription, DNA-dependent	chromosome|nuclear speck	C2H2 zinc finger domain binding|DNA binding|metal ion binding|protein N-terminus binding			cervix(1)|lung(2)|prostate(3)|skin(1)|stomach(1)	8	all_cancers(11;1.83e-25)|all_epithelial(7;9.19e-23)|Lung NSC(8;3.06e-15)|all_lung(8;5.05e-14)|Melanoma(16;0.000465)|Ovarian(15;0.0028)|Colorectal(54;0.0332)|all_neural(72;0.142)	Lung SC(17;0.0262)	LUSC - Lung squamous cell carcinoma(15;0.000204)|Lung(15;0.00494)|Epithelial(17;0.195)			TCCTGCATCGTCTGAGCCGGC	0.607000													21	143					0	0	1	0	0
SLC4A8	9498	broad.mit.edu	37	12	51855065	51855065	+	Missense_Mutation	SNP	T	T	A			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr12:51855065T>A	uc001rys.1	+	8	1269	c.1091T>A	c.(1090-1092)aTg>aAg	p.M364K	SLC4A8_uc010sni.2_Missense_Mutation_p.M311K|SLC4A8_uc001rym.3_Missense_Mutation_p.M311K|SLC4A8_uc001ryn.3_Missense_Mutation_p.M311K|SLC4A8_uc001ryo.2_Missense_Mutation_p.M311K|SLC4A8_uc001ryp.1_Missense_Mutation_p.M311K|SLC4A8_uc010snj.2_Missense_Mutation_p.M391K|SLC4A8_uc001ryq.4_Missense_Mutation_p.M364K|SLC4A8_uc001ryr.3_Missense_Mutation_p.M364K|SLC4A8_uc010snk.2_Missense_Mutation_p.M311K	NM_001039960	NP_001035049	Q2Y0W8	S4A8_HUMAN	Homo sapiens solute carrier family 4, sodium bicarbonate cotransporter, member 8 (SLC4A8), transcript variant 1, mRNA.	364					bicarbonate transport|sodium ion transport	integral to membrane|plasma membrane	inorganic anion exchanger activity			NS(1)|breast(2)|central_nervous_system(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(7)|lung(18)|ovary(3)|pancreas(1)|prostate(1)|skin(6)|stomach(2)|urinary_tract(5)	55				BRCA - Breast invasive adenocarcinoma(357;0.15)		GCCACCATCATGACAGATGAG	0.408000													3	41					0	0	1	0	0
KCNA10	3744	broad.mit.edu	37	1	111061227	111061227	+	Silent	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:111061227C>T	uc001dzt.1	-	0	571	c.183G>A	c.(181-183)acG>acA	p.T61T		NM_005549	NP_005540	Q16322	KCA10_HUMAN	Homo sapiens potassium voltage-gated channel, shaker-related subfamily, member 10 (KCNA10), mRNA.	61						voltage-gated potassium channel complex	intracellular cyclic nucleotide activated cation channel activity|voltage-gated potassium channel activity	p.T61T(2)|p.T61M(1)		endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(13)|lung(13)|ovary(3)|skin(1)|urinary_tract(1)	35		all_cancers(81;4.57e-06)|all_epithelial(167;1.52e-05)|all_lung(203;0.000152)|Lung NSC(277;0.000301)		Lung(183;0.0238)|all cancers(265;0.0874)|Colorectal(144;0.103)|Epithelial(280;0.116)|LUSC - Lung squamous cell carcinoma(189;0.134)		TGGAGAAGGCCGTCTCATGGT	0.582000													5	118					0	0	1	0	0
RSPH9	221421	broad.mit.edu	37	6	43623376	43623376	+	Silent	SNP	C	C	T			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr6:43623376C>T	uc003ovx.2	+	2	495	c.426C>T	c.(424-426)ggC>ggT	p.G142G	RSPH9_uc003ovw.2_Silent_p.G157G	NM_001193341	NP_001180270	Q9H1X1	RSPH9_HUMAN	Homo sapiens radial spoke head 9 homolog (Chlamydomonas) (RSPH9), transcript variant 2, mRNA.	157					cilium axoneme assembly|cilium movement	cytoplasm|cytoskeleton		p.G157G(1)		NS(1)|endometrium(2)|kidney(1)|large_intestine(5)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	12						TCCCCCGAGGCGCCCTCTTCA	0.572000									Kartagener syndrome				36	253					0	0	1	0	0
TMEM52	339456	broad.mit.edu	37	1	1850628	1850636	+	In_Frame_Del	DEL	AGCGGCAGG	AGCGGCAGG	-			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:1850628_1850636delAGCGGCAGG	uc001aij.2	-	0	105_113	c.69_77delCCTGCCGCT	c.(67-78)ctcctgccgctg>ctg	p.23_26LLPL>L	TMEM52_uc001aii.2_5'Flank	NM_178545	NP_848640	Q8NDY8	TMM52_HUMAN	Homo sapiens transmembrane protein 52 (TMEM52), mRNA.	23						integral to membrane				NS(1)|prostate(1)|stomach(1)	3	all_cancers(77;0.000708)|all_epithelial(69;0.000943)|all_lung(157;0.00963)|Lung NSC(156;0.0232)|Ovarian(185;0.0634)	all_epithelial(116;6.04e-15)|all_lung(118;9.67e-07)|Lung NSC(185;5.59e-05)|Renal(390;0.00571)|Breast(487;0.0183)|Hepatocellular(190;0.0268)|Myeloproliferative disorder(586;0.028)|Ovarian(437;0.127)|Medulloblastoma(700;0.151)|Lung SC(97;0.217)		Epithelial(90;1.82e-37)|OV - Ovarian serous cystadenocarcinoma(86;2.75e-23)|GBM - Glioblastoma multiforme(42;9e-08)|Colorectal(212;3.94e-05)|COAD - Colon adenocarcinoma(227;0.000193)|Kidney(185;0.00227)|BRCA - Breast invasive adenocarcinoma(365;0.00435)|STAD - Stomach adenocarcinoma(132;0.00644)|KIRC - Kidney renal clear cell carcinoma(229;0.0339)|Lung(427;0.199)		CACCTgcggcagcggcaggagcggcagga	0.766													4	3	---	---	---	---					
PCSK9	255738	broad.mit.edu	37	1	55505552	55505553	+	In_Frame_Ins	INS	-	-	CTG	rs35574083		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr1:55505552_55505553insCTG	uc001cyf.2	+	0	404_405	c.42_43insCTG	c.(40-45)insCTG	p.23_24insL	PCSK9_uc010ool.2_Non-coding_Transcript|PCSK9_uc010oom.2_5'Flank	NM_174936	NP_777596	Q8NBP7	PCSK9_HUMAN	Homo sapiens proprotein convertase subtilisin/kexin type 9 (PCSK9), mRNA.	23			L -> LL (this polymoprhism seems to have a modifier effect on LDLR mutation and familial hypercholesterolemia).		cellular response to insulin stimulus|cellular response to starvation|cholesterol homeostasis|cholesterol metabolic process|kidney development|liver development|low-density lipoprotein particle receptor catabolic process|lysosomal transport|negative regulation of catalytic activity|negative regulation of low-density lipoprotein particle clearance|negative regulation of receptor recycling|neuron differentiation|positive regulation of neuron apoptosis|positive regulation of receptor internalization|protein autoprocessing|regulation of receptor activity	extracellular space|late endosome|lysosome|perinuclear region of cytoplasm	apolipoprotein receptor binding|identical protein binding|low-density lipoprotein particle receptor binding|serine-type endopeptidase activity|very-low-density lipoprotein particle receptor binding	p.P14_L15insL(2)		NS(2)|breast(2)|central_nervous_system(3)|endometrium(3)|haematopoietic_and_lymphoid_tissue(2)|kidney(5)|large_intestine(1)|liver(2)|lung(4)|ovary(3)|prostate(3)|skin(1)|urinary_tract(1)	32						Ggccgctgccactgctgctgct	0.703													6	5	---	---	---	---					
ATP6V1H	51606	broad.mit.edu	37	8	54754237	54754238	+	Frame_Shift_Ins	INS	-	-	C			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr8:54754237_54754238insC	uc003xrl.3	-	1	165_166	c.13_14insG	c.(13-15)gatfs	p.D5fs	ATP6V1H_uc003xrk.3_5'Flank|ATP6V1H_uc003xrm.3_Frame_Shift_Ins_p.D5fs|ATP6V1H_uc003xrn.3_Frame_Shift_Ins_p.D5fs|ATP6V1H_uc011ldv.2_5'UTR|ATP6V1H_uc010lyd.3_5'UTR	NM_213620	NP_998785	Q9UI12	VATH_HUMAN	Homo sapiens ATPase, H+ transporting, lysosomal 50/57kDa, V1 subunit H (ATP6V1H), transcript variant 3, mRNA.	5					ATP hydrolysis coupled proton transport|cellular iron ion homeostasis|endocytosis|insulin receptor signaling pathway|interspecies interaction between organisms|regulation of defense response to virus by virus|transferrin transport|vacuolar acidification|viral reproduction	cytosol|plasma membrane|vacuolar proton-transporting V-type ATPase, V1 domain	enzyme regulator activity|protein binding|proton-transporting ATPase activity, rotational mechanism			endometrium(3)|large_intestine(5)|lung(8)|ovary(1)|urinary_tract(1)	18		all_epithelial(80;0.0487)|Lung NSC(129;0.109)|all_lung(136;0.181)	OV - Ovarian serous cystadenocarcinoma(7;2.79e-06)|Epithelial(17;0.000629)|all cancers(17;0.00359)			ACCTCGGATATCCATTTTGGTC	0.396													15	134	---	---	---	---					
MON1B	22879	broad.mit.edu	37	16	77228355	77228380	+	Frame_Shift_Del	DEL	CACTTACACGTGCAAGTGTCGCCCGC	CACTTACACGTGCAAGTGTCGCCCGC	-			TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr16:77228355_77228380delCACTTACACGTGCAAGTGTCGCCCGC	uc002fez.3	+	3	929_954	c.599_624delCACTTACACGTGCAAGTGTCGCCCGC	c.(598-624)acacttacacgtgcaagtgtcgcccgcfs	p.T200fs	MON1B_uc010vnf.2_Frame_Shift_Del_p.T91fs|MON1B_uc010vng.2_Frame_Shift_Del_p.T54fs|MON1B_uc002ffa.3_Frame_Shift_Del_p.T80fs	NM_014940	NP_055755	Q7L1V2	MON1B_HUMAN	Homo sapiens MON1 homolog B (yeast) (MON1B), mRNA.	200							protein binding			breast(1)|endometrium(5)|kidney(1)|large_intestine(5)|lung(3)|ovary(1)|upper_aerodigestive_tract(1)	17						ATCGTGAGCACACTTACACGTGCAAGTGTCGCCCGCATCTTCGCAC	0.611													12	158	---	---	---	---					
POLI	11201	broad.mit.edu	37	18	51795958	51795960	+	In_Frame_Del	DEL	CGA	CGA	-	rs140689079		TCGA-HC-7817-01B-11D-A29Q-08	TCGA-HC-7817-10A-01D-A29Q-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	cbec5e2a-4b00-4c72-ab57-6594b7901be0	c62fbae9-4356-4b26-8b3f-daf9c77e3a62	g.chr18:51795958_51795960delCGA	uc002lfj.4	+	0	110_112	c.42_44delCGA	c.(40-45)ggcgac>ggc	p.D17del	POLI_uc010xds.2_In_Frame_Del_p.D17del|POLI_uc002lfk.4_5'UTR|POLI_uc002lfl.1_5'Flank	NM_007195	NP_009126	Q9UNA4	POLI_HUMAN	Homo sapiens polymerase (DNA directed) iota (POLI), mRNA.	17					DNA repair|DNA replication	nucleoplasm	DNA-directed DNA polymerase activity|damaged DNA binding|metal ion binding|protein binding	p.D17delD(1)		breast(1)|endometrium(4)|kidney(2)|large_intestine(10)|lung(5)|ovary(3)|urinary_tract(1)	26				Colorectal(16;0.0234)|READ - Rectum adenocarcinoma(59;0.197)		AAGGCGGCGGCGACGACGACGAG	0.729								DNA polymerases (catalytic subunits)					8	3	---	---	---	---					
