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
CHD5	26038	broad.mit.edu	37	1	6184051	6184051	+	Silent	SNP	G	G	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:6184051G>C	uc001amb.2	-	30	4767	c.4656C>G	c.(4654-4656)ccC>ccG	p.P1552P	CHD5_uc001alz.2_Silent_p.P409P|CHD5_uc001ama.2_Non-coding_Transcript|CHD5_uc001amc.1_Non-coding_Transcript	NM_015557	NP_056372	Q8TDI0	CHD5_HUMAN	Homo sapiens chromodomain helicase DNA binding protein 5 (CHD5), mRNA.	1552					chromatin modification|regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	ATP binding|ATP-dependent helicase activity|DNA binding|zinc ion binding			breast(3)|central_nervous_system(3)|liver(1)|lung(1)|ovary(4)|pancreas(1)|skin(1)|upper_aerodigestive_tract(2)	16	Ovarian(185;0.0634)	all_cancers(23;5.36e-32)|all_epithelial(116;2.32e-17)|all_neural(13;3.68e-06)|all_lung(118;3.94e-06)|all_hematologic(16;2.39e-05)|Lung NSC(185;5.33e-05)|Acute lymphoblastic leukemia(12;0.000372)|Glioma(11;0.00127)|Renal(390;0.00188)|Colorectal(325;0.00342)|Breast(487;0.00373)|Hepatocellular(190;0.0218)|Myeloproliferative disorder(586;0.0393)|Ovarian(437;0.15)		Epithelial(90;3.08e-37)|GBM - Glioblastoma multiforme(13;1.36e-31)|OV - Ovarian serous cystadenocarcinoma(86;7.7e-19)|Colorectal(212;9.97e-08)|COAD - Colon adenocarcinoma(227;1.07e-05)|Kidney(185;6.16e-05)|KIRC - Kidney renal clear cell carcinoma(229;0.00109)|BRCA - Breast invasive adenocarcinoma(365;0.0012)|STAD - Stomach adenocarcinoma(132;0.00346)|READ - Rectum adenocarcinoma(331;0.0649)|Lung(427;0.193)		CAGGGCTGGCGGGCACTGGTG	0.677												
PEX14	5195	broad.mit.edu	37	1	10555343	10555343	+	Missense_Mutation	SNP	C	C	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:10555343C>G	uc001arn.3	+	1	70	c.49C>G	c.(49-51)Cca>Gca	p.P17A	PEX14_uc001arm.1_Non-coding_Transcript|PEX14_uc009vmu.1_Missense_Mutation_p.P17A|PEX14_uc009vmv.3_5'UTR|PEX14_uc010oam.2_5'UTR|PEX14_uc010oan.2_Missense_Mutation_p.P17A|PEX14_uc001arl.3_Non-coding_Transcript	NM_004565	NP_004556	O75381	PEX14_HUMAN	Homo sapiens peroxisomal biogenesis factor 14 (PEX14), mRNA.	17					negative regulation of sequence-specific DNA binding transcription factor activity|negative regulation of transcription, DNA-dependent|protein homooligomerization|protein import into peroxisome matrix|transmembrane transport	integral to membrane|nucleus|peroxisomal membrane|protein complex	protein N-terminus binding|transcription corepressor activity			breast(3)|endometrium(1)|large_intestine(3)|lung(5)|prostate(1)	13	Ovarian(185;0.203)	all_lung(284;6.02e-06)|Lung NSC(185;9.62e-06)|Renal(390;0.000147)|Breast(348;0.000932)|Colorectal(325;0.00215)|Hepatocellular(190;0.00913)|Ovarian(437;0.023)|Myeloproliferative disorder(586;0.0255)		UCEC - Uterine corpus endometrioid carcinoma (279;0.0292)|Colorectal(212;9.13e-08)|COAD - Colon adenocarcinoma(227;2.07e-05)|BRCA - Breast invasive adenocarcinoma(304;0.000482)|Kidney(185;0.00174)|KIRC - Kidney renal clear cell carcinoma(229;0.00457)|STAD - Stomach adenocarcinoma(132;0.0249)|READ - Rectum adenocarcinoma(331;0.0419)		AAGCTCTACTCCAGGAAGTGA	0.428											OREG0013090	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
UBR4	23352	broad.mit.edu	37	1	19412732	19412732	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:19412732G>A	uc001bbi.3	-	100	14724	c.14720C>T	c.(14719-14721)gCc>gTc	p.A4907V	UBR4_uc010ocv.2_Missense_Mutation_p.A430V|UBR4_uc009vph.3_Missense_Mutation_p.A541V|UBR4_uc010ocw.2_Missense_Mutation_p.A571V|UBR4_uc001bbg.3_Missense_Mutation_p.A618V|UBR4_uc001bbh.3_Missense_Mutation_p.A616V	NM_020765	NP_065816	Q5T4S7	UBR4_HUMAN	Homo sapiens ubiquitin protein ligase E3 component n-recognin 4 (UBR4), mRNA.	4907					interspecies interaction between organisms	cytoplasm|cytoskeleton|integral to membrane|nucleus	calmodulin binding|ubiquitin-protein ligase activity|zinc ion binding			breast(7)|central_nervous_system(1)|cervix(2)|endometrium(23)|kidney(25)|large_intestine(25)|liver(2)|lung(47)|ovary(10)|pancreas(2)|prostate(7)|skin(5)|stomach(5)|upper_aerodigestive_tract(4)|urinary_tract(6)	171		Colorectal(325;3.46e-05)|Renal(390;0.000147)|all_lung(284;0.000328)|Lung NSC(340;0.000406)|Breast(348;0.000814)|Ovarian(437;0.00774)|Myeloproliferative disorder(586;0.0256)		UCEC - Uterine corpus endometrioid carcinoma (279;0.00674)|BRCA - Breast invasive adenocarcinoma(304;5.43e-05)|Kidney(64;0.000337)|KIRC - Kidney renal clear cell carcinoma(64;0.00426)|STAD - Stomach adenocarcinoma(196;0.00715)|READ - Rectum adenocarcinoma(331;0.0816)		CTGCAGGGCGGCACTCTCCCA	0.612												
FUCA1	2517	broad.mit.edu	37	1	24180899	24180899	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:24180899C>T	uc001bie.3	-	4	1003	c.920G>A	c.(919-921)cGt>cAt	p.R307H	FUCA1_uc009vqt.2_Non-coding_Transcript	NM_000147	NP_000138	P04066	FUCO_HUMAN	Homo sapiens fucosidase, alpha-L- 1, tissue (FUCA1), mRNA.	307					fucose metabolic process|glycosaminoglycan catabolic process	lysosome	alpha-L-fucosidase activity|cation binding			breast(1)|endometrium(1)|large_intestine(3)|lung(3)	8		Colorectal(325;3.46e-05)|Renal(390;0.000219)|Lung NSC(340;0.000233)|all_lung(284;0.000321)|Ovarian(437;0.00348)|Breast(348;0.00957)|Myeloproliferative disorder(586;0.0255)		UCEC - Uterine corpus endometrioid carcinoma (279;0.0228)|OV - Ovarian serous cystadenocarcinoma(117;1.11e-24)|Colorectal(126;5.69e-08)|COAD - Colon adenocarcinoma(152;3.15e-06)|GBM - Glioblastoma multiforme(114;9.04e-06)|BRCA - Breast invasive adenocarcinoma(304;0.000986)|KIRC - Kidney renal clear cell carcinoma(1967;0.00342)|STAD - Stomach adenocarcinoma(196;0.0128)|READ - Rectum adenocarcinoma(331;0.0649)|Lung(427;0.144)		CATGTCACGACGATAGCCCCA	0.393												
PTPRF	5792	broad.mit.edu	37	1	44084401	44084401	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:44084401G>A	uc001cjr.3	+	25	4812	c.4472G>A	c.(4471-4473)cGc>cAc	p.R1491H	PTPRF_uc001cjs.3_Missense_Mutation_p.R1482H|PTPRF_uc001cju.3_Missense_Mutation_p.R880H|PTPRF_uc009vwt.3_Missense_Mutation_p.R1051H|PTPRF_uc001cjv.3_Missense_Mutation_p.R962H|PTPRF_uc001cjw.3_Missense_Mutation_p.R717H	NM_002840	NP_002831	P10586	PTPRF_HUMAN	Homo sapiens protein tyrosine phosphatase, receptor type, F (PTPRF), transcript variant 1, mRNA.	1491	Tyrosine-protein phosphatase 1.				transmembrane receptor protein tyrosine phosphatase signaling pathway	integral to plasma membrane	transmembrane receptor protein tyrosine phosphatase activity			NS(2)|breast(4)|central_nervous_system(3)|endometrium(9)|kidney(4)|large_intestine(11)|liver(1)|lung(24)|ovary(4)|prostate(2)|skin(5)|upper_aerodigestive_tract(3)	72	all_hematologic(146;0.0958)|Acute lymphoblastic leukemia(166;0.155)	Myeloproliferative disorder(586;0.0333)				TACACTGTGCGCACCTTCGCA	0.572												
MUTYH	4595	broad.mit.edu	37	1	45797967	45797967	+	Silent	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:45797967C>T	uc001cnm.3	-	9	1011	c.795G>A	c.(793-795)caG>caA	p.Q265Q	MUTYH_uc001cnf.3_Silent_p.Q240Q|MUTYH_uc009vxo.3_Silent_p.Q240Q|MUTYH_uc001cng.3_Silent_p.Q251Q|MUTYH_uc001cnj.3_Silent_p.Q148Q|MUTYH_uc001cni.3_Silent_p.Q240Q|MUTYH_uc001cnh.3_Silent_p.Q241Q|MUTYH_uc001cnl.3_Silent_p.Q254Q|MUTYH_uc009vxp.3_Silent_p.Q268Q|MUTYH_uc001cnn.3_Silent_p.Q255Q|MUTYH_uc001cno.3_Silent_p.Q148Q|MUTYH_uc010oll.2_Intron	NM_012222	NP_036354	Q9UIF7	MUTYH_HUMAN	Homo sapiens mutY homolog (E. coli) (MUTYH), transcript variant alpha1, mRNA.	265					depurination|mismatch repair	nucleoplasm	4 iron, 4 sulfur cluster binding|DNA N-glycosylase activity|endonuclease activity|metal ion binding|MutSalpha complex binding			NS(1)|central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(5)|lung(8)|urinary_tract(1)	19	Acute lymphoblastic leukemia(166;0.155)					GGTCCACCAGCTGCTGGGCTA	0.597			Mis			colorectal		Base excision repair (BER), DNA glycosylases	MUTYH-associated polyposis			
DENND2C	163259	broad.mit.edu	37	1	115167981	115167981	+	Missense_Mutation	SNP	G	G	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:115167981G>C	uc001efd.1	-	3	1327	c.625C>G	c.(625-627)Cct>Gct	p.P209A	DENND2C_uc001eez.3_Non-coding_Transcript|DENND2C_uc001efc.1_Missense_Mutation_p.P209A	NM_198459	NP_940861	Q68D51	DEN2C_HUMAN	Homo sapiens DENN/MADD domain containing 2C (DENND2C), transcript variant 2, mRNA.	209										NS(2)|breast(2)|cervix(2)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(10)|lung(10)|pancreas(1)|skin(3)	37	all_epithelial(7;9.54e-05)|all_lung(7;0.000179)|Lung NSC(6;0.00195)|Lung SC(450;0.211)	all_cancers(81;4.64e-07)|all_epithelial(167;4.2e-07)|all_lung(203;9.97e-06)|Lung NSC(69;1.74e-05)		Lung(183;0.0234)|Colorectal(144;0.0686)|COAD - Colon adenocarcinoma(174;0.111)|all cancers(265;0.112)|Epithelial(280;0.124)|LUSC - Lung squamous cell carcinoma(189;0.133)		TTTGGCAAAGGATTTATGGAA	0.378												
NBPF10	100132406	broad.mit.edu	37	1	145302676	145302676	+	Missense_Mutation	SNP	G	G	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:145302676G>T	uc021oul.1	+	7	1149	c.1114G>T	c.(1114-1116)Gct>Tct	p.A372S	NBPF10_uc021ots.1_Intron|NBPF10_uc010oye.2_Intron|NBPF10_uc021ouk.1_Missense_Mutation_p.A372S|NBPF10_uc010oyi.2_5'UTR|NBPF10_uc001emq.1_Missense_Mutation_p.A101S|NBPF10_uc021oum.1_5'Flank	NM_001039703	NP_001034792	A6NDV3	A6NDV3_HUMAN	Homo sapiens neuroblastoma breakpoint family, member 10 (NBPF10), mRNA.	372										NS(3)|breast(1)|central_nervous_system(3)|endometrium(12)|kidney(23)|lung(15)|ovary(1)|prostate(7)|skin(6)|urinary_tract(2)	73	all_hematologic(923;0.032)			Colorectal(1306;1.36e-07)|KIRC - Kidney renal clear cell carcinoma(1967;0.00258)		CCTGGTTCACGCTCAGGAACG	0.483												
HIST2H3D	653604	broad.mit.edu	37	1	149785226	149785226	+	Missense_Mutation	SNP	G	G	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:149785226G>C	uc010pbl.2	-	0	11	c.11C>G	c.(10-12)aCt>aGt	p.T4S	HIST2H2BF_uc010pbj.2_5'Flank|HIST2H2BF_uc010pbk.2_5'Flank|HIST2H2BF_uc001esr.3_5'Flank	NM_001123375	NP_001116847	Q71DI3	H32_HUMAN	Homo sapiens histone cluster 2, H3d (HIST2H3D), mRNA.	4					blood coagulation|nucleosome assembly	nucleoplasm|nucleosome	DNA binding|protein binding			biliary_tract(1)|endometrium(1)|large_intestine(1)|liver(1)|lung(3)	7						AGTCTGCTTAGTACGGGCCAT	0.567												
FLG	2312	broad.mit.edu	37	1	152285914	152285914	+	Missense_Mutation	SNP	C	C	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:152285914C>A	uc001ezu.1	-	2	1484	c.1448G>T	c.(1447-1449)gGa>gTa	p.G483V	AK056431_uc001ezv.3_5'Flank	NM_002016	NP_002007	P20930	FILA_HUMAN	Homo sapiens filaggrin (FLG), mRNA.	483	Ser-rich.				keratinocyte differentiation	cytoplasmic membrane-bounded vesicle|intermediate filament	calcium ion binding|structural molecule activity			autonomic_ganglia(1)|breast(13)|central_nervous_system(5)|cervix(2)|endometrium(38)|haematopoietic_and_lymphoid_tissue(1)|kidney(16)|large_intestine(57)|lung(211)|ovary(13)|pancreas(1)|prostate(15)|skin(24)|stomach(5)|upper_aerodigestive_tract(10)|urinary_tract(12)	424	Hepatocellular(266;0.0877)|Melanoma(130;0.116)|all_hematologic(923;0.127)		LUSC - Lung squamous cell carcinoma(543;0.206)			CCCGGTCCGTCCATGGGCAGA	0.607									Ichthyosis			
UBAP2L	9898	broad.mit.edu	37	1	154242707	154242707	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:154242707C>T	uc001fep.4	+	26	3367	c.3200C>T	c.(3199-3201)tCc>tTc	p.S1067F	UBAP2L_uc010pel.2_Intron|UBAP2L_uc001feq.3_Intron|UBAP2L_uc001fer.3_Missense_Mutation_p.S280F|HAX1_uc001fet.3_5'Flank|HAX1_uc001fes.3_5'Flank|HAX1_uc010peo.2_5'Flank|HAX1_uc009wou.3_5'Flank	NM_014847	NP_055662	Q14157	UBP2L_HUMAN	Homo sapiens ubiquitin associated protein 2-like (UBAP2L), transcript variant 1, mRNA.	1067					binding of sperm to zona pellucida		protein binding			NS(2)|breast(7)|central_nervous_system(1)|endometrium(7)|kidney(1)|large_intestine(8)|lung(20)|ovary(1)|prostate(1)|urinary_tract(2)	50	all_lung(78;1.09e-30)|Lung NSC(65;1.66e-28)|Hepatocellular(266;0.0877)		LUSC - Lung squamous cell carcinoma(543;0.185)			CAGACCAGCTCCATCCCGCAG	0.562												
SMG7	9887	broad.mit.edu	37	1	183486872	183486872	+	Missense_Mutation	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr1:183486872A>G	uc001gqg.3	+	3	479	c.229A>G	c.(229-231)Aag>Gag	p.K77E	SMG7_uc010pob.2_Missense_Mutation_p.K106E|SMG7_uc021pga.1_Missense_Mutation_p.K35E|SMG7_uc001gqf.3_Missense_Mutation_p.K77E|SMG7_uc001gqh.3_Missense_Mutation_p.K77E|SMG7_uc010poc.2_Missense_Mutation_p.K35E	NM_173156	NP_775179	Q92540	SMG7_HUMAN	Homo sapiens smg-7 homolog, nonsense mediated mRNA decay factor (C. elegans) (SMG7), transcript variant 1, mRNA.	77					mRNA export from nucleus|nuclear-transcribed mRNA catabolic process, nonsense-mediated decay|regulation of dephosphorylation	cytoplasm|intermediate filament cytoskeleton|nucleus	protein phosphatase 2A binding			breast(1)|central_nervous_system(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(2)|kidney(2)|large_intestine(7)|lung(16)|prostate(3)|skin(5)|upper_aerodigestive_tract(1)|urinary_tract(1)	46						AGGCCAGGCAAAGAATCGAGC	0.443												
FAM196A	642938	broad.mit.edu	37	10	128974485	128974485	+	Nonsense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr10:128974485G>A	uc001lju.1	-	0	216	c.175C>T	c.(175-177)Cag>Tag	p.Q59*	DOCK1_uc001ljt.3_Intron|DOCK1_uc010qun.2_Intron|FAM196A_uc010quo.1_Nonsense_Mutation_p.Q59*|FAM196A_uc001ljv.1_Nonsense_Mutation_p.Q59*|FAM196A_uc009yap.1_Nonsense_Mutation_p.Q59*	NM_001039762	NP_001034851	Q6ZSG2	F196A_HUMAN	Homo sapiens family with sequence similarity 196, member A (FAM196A), mRNA.	59										breast(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(4)|lung(13)|ovary(2)|prostate(2)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)	30						GTGTCCCTCTGCTCATTCTGT	0.587												
LUZP2	338645	broad.mit.edu	37	11	25100153	25100153	+	Silent	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr11:25100153A>G	uc001mqs.3	+	11	1264	c.990A>G	c.(988-990)aaA>aaG	p.K330K	LUZP2_uc009yif.3_Silent_p.K244K|LUZP2_uc009yig.3_Silent_p.K288K	NM_001009909	NP_001009909	Q86TE4	LUZP2_HUMAN	Homo sapiens leucine zipper protein 2 (LUZP2), transcript variant 1, mRNA.	330						extracellular region				central_nervous_system(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(3)|large_intestine(11)|lung(12)|ovary(1)|skin(2)|upper_aerodigestive_tract(1)	32						CCCCAGAAAAACCATTGACCA	0.348												
TRIM51	84767	broad.mit.edu	37	11	55655555	55655555	+	Missense_Mutation	SNP	G	G	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr11:55655555G>T	uc010rip.2	+	3	647	c.555G>T	c.(553-555)aaG>aaT	p.K185N	TRIM51_uc010riq.2_Missense_Mutation_p.K42N	NM_032681	NP_116070	Q9BSJ1	SPRY5_HUMAN	Homo sapiens SPRY domain containing 5 (SPRYD5), mRNA.	185						intracellular	zinc ion binding										AATATCAGAAGATGCCTGCAT	0.398												
ARHGAP20	57569	broad.mit.edu	37	11	110495025	110495025	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr11:110495025T>C	uc001pkz.1	-	4	649	c.364A>G	c.(364-366)Aac>Gac	p.N122D	ARHGAP20_uc001pky.1_Missense_Mutation_p.N99D|ARHGAP20_uc009yyb.1_Missense_Mutation_p.N86D|ARHGAP20_uc001pla.1_Missense_Mutation_p.N86D	NM_020809	NP_065860	Q9P2F6	RHG20_HUMAN	Homo sapiens Rho GTPase activating protein 20 (ARHGAP20), mRNA.	122	PH.				regulation of small GTPase mediated signal transduction|small GTPase mediated signal transduction	cytosol	GTPase activator activity			breast(1)|central_nervous_system(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(8)|large_intestine(18)|lung(13)|ovary(4)|prostate(2)|skin(4)|upper_aerodigestive_tract(1)	60		all_cancers(61;3.26e-12)|all_epithelial(67;6.09e-07)|Melanoma(852;1.46e-05)|all_hematologic(158;0.000484)|Acute lymphoblastic leukemia(157;0.000967)|all_neural(223;0.0199)|Medulloblastoma(222;0.0425)|Breast(348;0.0544)		Epithelial(105;3.05e-06)|BRCA - Breast invasive adenocarcinoma(274;1.24e-05)|all cancers(92;0.000147)|OV - Ovarian serous cystadenocarcinoma(223;0.0475)		atCTTAAAGTTATTGTTATAT	0.333												
TMPRSS13	84000	broad.mit.edu	37	11	117789400	117789400	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr11:117789400C>T	uc001prs.2	-	1	321	c.175G>A	c.(175-177)Gca>Aca	p.A59T	TMPRSS13_uc009yzr.2_Missense_Mutation_p.A59T|TMPRSS13_uc021qrc.1_Missense_Mutation_p.A59T|TMPRSS13_uc001prt.1_5'UTR|TMPRSS13_uc001pru.2_Missense_Mutation_p.A59T	NM_001077263	NP_001070731	Q9BYE2	TMPSD_HUMAN	Homo sapiens transmembrane protease, serine 13 (TMPRSS13), transcript variant 1, mRNA.	59	12 X 5 AA repeats of A-S-P-A-[GLQR].|4 X 5 AA repeats of T-P-P-G-R.|Ala-rich.				proteolysis	integral to membrane	scavenger receptor activity|serine-type endopeptidase activity			endometrium(1)|kidney(3)|large_intestine(6)|lung(7)|pancreas(1)|prostate(1)|urinary_tract(1)	20	all_hematologic(175;0.0487)	Medulloblastoma(222;0.0425)|all_hematologic(192;0.196)|all_neural(223;0.234)		BRCA - Breast invasive adenocarcinoma(274;1.78e-05)|Epithelial(105;0.00106)		GCTGGAGATGCCTGGGCTGGA	0.697												
TREH	11181	broad.mit.edu	37	11	118530175	118530175	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr11:118530175T>C	uc001pty.1	-	11	1381	c.1336A>G	c.(1336-1338)Act>Gct	p.T446A	TREH_uc009zaj.1_Missense_Mutation_p.T415A|TREH_uc001ptz.1_Missense_Mutation_p.T323A	NM_007180	NP_009111	O43280	TREA_HUMAN	Homo sapiens trehalase (brush-border membrane glycoprotein) (TREH), mRNA.	446					polysaccharide digestion|trehalose catabolic process	anchored to plasma membrane	alpha,alpha-trehalase activity			NS(1)|endometrium(1)|kidney(3)|large_intestine(2)|lung(3)|ovary(1)|pancreas(1)|urinary_tract(1)	13	all_hematologic(175;0.0839)	Medulloblastoma(222;0.0425)|all_hematologic(192;0.0564)|all_neural(223;0.112)		BRCA - Breast invasive adenocarcinoma(274;3.16e-05)		TACTGGTAAGTCAGGATCCGG	0.617											OREG0021385	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
CCND2	894	broad.mit.edu	37	12	4398029	4398029	+	Missense_Mutation	SNP	C	C	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:4398029C>G	uc001qmo.3	+	3	898	c.593C>G	c.(592-594)cCa>cGa	p.P198R		NM_001759	NP_001750	P30279	CCND2_HUMAN	Homo sapiens cyclin D2 (CCND2), mRNA.	198					cell division|positive regulation of cyclin-dependent protein kinase activity|positive regulation of protein phosphorylation	cyclin-dependent protein kinase holoenzyme complex|cytoplasm|membrane|nucleus	protein kinase binding			breast(1)|central_nervous_system(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(1)|lung(7)|prostate(1)|upper_aerodigestive_tract(1)	17			all cancers(3;4.15e-10)|GBM - Glioblastoma multiforme(3;6.34e-05)|Colorectal(7;0.00245)|OV - Ovarian serous cystadenocarcinoma(31;0.00301)|COAD - Colon adenocarcinoma(12;0.0264)|STAD - Stomach adenocarcinoma(119;0.206)			GCCATGTACCCACCGTCGATG	0.547			T	IGL@	"""NHL,CLL"""							
ACSM4	341392	broad.mit.edu	37	12	7470689	7470689	+	Missense_Mutation	SNP	G	G	A	rs79217312		TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:7470689G>A	uc001qsx.1	+	4	832	c.832G>A	c.(832-834)Gcc>Acc	p.A278T		NM_001080454	NP_001073923	P0C7M7	ACSM4_HUMAN	Homo sapiens acyl-CoA synthetase medium-chain family member 4 (ACSM4), mRNA.	278					fatty acid metabolic process	mitochondrial matrix	ATP binding|butyrate-CoA ligase activity|metal ion binding	p.A278T(3)		endometrium(6)|kidney(1)|lung(14)	21						GGTCAAGGCCGCCATTGGCAG	0.458												
MRPS35	60488	broad.mit.edu	37	12	27908375	27908375	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:27908375G>A	uc001rih.3	+	7	1035	c.964G>A	c.(964-966)Gtg>Atg	p.V322M	MRPS35_uc001rii.3_3'UTR	NM_021821	NP_068593	P82673	RT35_HUMAN	Homo sapiens mitochondrial ribosomal protein S35 (MRPS35), nuclear gene encoding mitochondrial protein, transcript variant 1, mRNA.	322					DNA damage response, detection of DNA damage	mitochondrial small ribosomal subunit				breast(1)|endometrium(1)|kidney(1)|lung(2)|urinary_tract(1)	6	Lung SC(9;0.0873)					ACTATTAAATGTGACATGAAT	0.254												
GLI1	2735	broad.mit.edu	37	12	57864118	57864118	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:57864118G>A	uc001snx.3	+	11	1689	c.1595G>A	c.(1594-1596)cGc>cAc	p.R532H	GLI1_uc021qzi.1_Missense_Mutation_p.R491H|GLI1_uc009zpq.3_Missense_Mutation_p.R404H	NM_005269	NP_001153517	P08151	GLI1_HUMAN	Homo sapiens GLI family zinc finger 1 (GLI1), transcript variant 1, mRNA.	532					epidermal cell differentiation|negative regulation of canonical Wnt receptor signaling pathway|osteoblast differentiation|positive regulation of DNA replication|positive regulation of smoothened signaling pathway|positive regulation of transcription from RNA polymerase II promoter	cytosol|nucleus	transcription regulatory region DNA binding|zinc ion binding			NS(1)|breast(7)|central_nervous_system(1)|cervix(1)|endometrium(5)|haematopoietic_and_lymphoid_tissue(4)|kidney(2)|large_intestine(8)|lung(22)|ovary(6)|pancreas(2)|prostate(2)|skin(5)|upper_aerodigestive_tract(2)|urinary_tract(1)	69			GBM - Glioblastoma multiforme(3;3.99e-32)			GTGTCCCGCCGCGTGGGCCCC	0.602												
SLC6A15	55117	broad.mit.edu	37	12	85270346	85270346	+	Missense_Mutation	SNP	A	A	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:85270346A>T	uc001szv.3	-	5	1290	c.797T>A	c.(796-798)aTt>aAt	p.I266N	SLC6A15_uc010sul.2_Missense_Mutation_p.I159N	NM_182767	NP_001139807	Q9H2J7	S6A15_HUMAN	Homo sapiens solute carrier family 6 (neutral amino acid transporter), member 15 (SLC6A15), transcript variant 1, mRNA.	266					cellular nitrogen compound metabolic process|leucine transport|proline transport	integral to plasma membrane	amino acid transmembrane transporter activity|neurotransmitter:sodium symporter activity	p.I266T(2)		kidney(1)|large_intestine(18)|lung(15)|ovary(1)|pancreas(2)|prostate(4)|skin(2)|upper_aerodigestive_tract(1)	44						GAGGAAGCAAATAAGTACCAC	0.303												
KNTC1	9735	broad.mit.edu	37	12	123014673	123014673	+	Silent	SNP	T	T	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr12:123014673T>G	uc001ucv.3	+	1	226	c.63T>G	c.(61-63)ggT>ggG	p.G21G	KNTC1_uc010taf.2_Silent_p.G21G	NM_014708	NP_055523	P50748	KNTC1_HUMAN	Homo sapiens kinetochore associated 1 (KNTC1), mRNA.	21					cell division|mitotic cell cycle checkpoint|mitotic prometaphase|protein complex assembly|regulation of exit from mitosis	condensed chromosome kinetochore|cytosol|kinetochore microtubule|nucleus|spindle pole	protein binding			breast(1)|central_nervous_system(1)|cervix(2)|endometrium(12)|kidney(8)|large_intestine(12)|lung(20)|ovary(7)|prostate(1)|skin(1)|upper_aerodigestive_tract(3)|urinary_tract(4)	72	all_neural(191;0.0837)|Medulloblastoma(191;0.163)			OV - Ovarian serous cystadenocarcinoma(86;7.21e-05)|Epithelial(86;0.000178)|BRCA - Breast invasive adenocarcinoma(302;0.217)		TGAGTGTCGGTTCAAGAAAAG	0.403												
ATP12A	479	broad.mit.edu	37	13	25263441	25263441	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr13:25263441G>A	uc010aaa.3	+	4	807	c.474G>A	c.(472-474)acG>acA	p.T158T	ATP12A_uc001upp.3_Silent_p.T158T	NM_001185085	NP_001172014	P54707	AT12A_HUMAN	Homo sapiens ATPase, H+/K+ transporting, nongastric, alpha polypeptide (ATP12A), transcript variant 1, mRNA.	158					ATP biosynthetic process	hydrogen:potassium-exchanging ATPase complex	ATP binding|hydrogen:potassium-exchanging ATPase activity|metal ion binding	p.T158M(1)		breast(6)|central_nervous_system(4)|endometrium(3)|kidney(5)|large_intestine(23)|lung(23)|ovary(2)|pancreas(1)|prostate(2)|skin(5)	74		Lung SC(185;0.0225)|Breast(139;0.077)		all cancers(112;0.0307)|Epithelial(112;0.086)|OV - Ovarian serous cystadenocarcinoma(117;0.228)	Esomeprazole(DB00736)|Pantoprazole(DB00213)	TCATTTTAACGGGGATCTTTG	0.537												
KIAA1704	55425	broad.mit.edu	37	13	45580365	45580367	+	In_Frame_Del	DEL	GAT	GAT	-	rs138421508		TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr13:45580365_45580367delGAT	uc001uzq.3	+	2	353_355	c.250_252delGAT	c.(250-252)gatdel	p.D88del	KIAA1704_uc010tfo.1_Non-coding_Transcript|KIAA1704_uc001uzr.1_In_Frame_Del_p.D88del|KIAA1704_uc001uzs.3_5'UTR|KIAA1704_uc001uzt.3_5'UTR	NM_018559	NP_061029	Q8IXQ4	K1704_HUMAN	Homo sapiens KIAA1704 (KIAA1704), mRNA.	88	Poly-Asp.									breast(1)|endometrium(1)|kidney(2)|large_intestine(3)|lung(1)|pancreas(1)|prostate(2)|skin(1)	12		Lung NSC(96;0.00143)|Prostate(109;0.0137)|Breast(139;0.0192)|Lung SC(185;0.0367)|Hepatocellular(98;0.133)	KIRC - Kidney renal clear cell carcinoma(16;0.234)	GBM - Glioblastoma multiforme(144;0.000313)|BRCA - Breast invasive adenocarcinoma(63;0.126)		Ggatgatgacgatgatgatgatg	0.335												
TTC5	91875	broad.mit.edu	37	14	20767565	20767565	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr14:20767565G>A	uc001vwt.3	-	3	496	c.439C>T	c.(439-441)Cgt>Tgt	p.R147C	TTC5_uc001vwu.3_Missense_Mutation_p.R4C	NM_138376	NP_612385	Q8N0Z6	TTC5_HUMAN	Homo sapiens tetratricopeptide repeat domain 5 (TTC5), mRNA.	147					DNA repair	cytoplasm|nucleus	binding			endometrium(1)|kidney(2)|large_intestine(3)|lung(7)|ovary(1)|prostate(1)	15	all_cancers(95;0.00092)		Epithelial(56;1.1e-06)|all cancers(55;8.07e-06)	GBM - Glioblastoma multiforme(265;0.0106)		CGCAGCTGACGAAGCACCATT	0.493												
ISM2	145501	broad.mit.edu	37	14	77948978	77948978	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr14:77948978G>A	uc001xtz.3	-	3	734	c.660C>T	c.(658-660)gcC>gcT	p.A220A	ISM2_uc001xua.3_Intron|ISM2_uc001xty.3_Silent_p.A132A	NM_199296	NP_954993	Q6H9L7	ISM2_HUMAN	Homo sapiens isthmin 2 homolog (zebrafish) (ISM2), transcript variant 1, mRNA.	220						extracellular region		p.A220A(2)		endometrium(3)|large_intestine(4)|lung(11)|prostate(1)|skin(1)|urinary_tract(1)	21						TCGACACCTCGGCCTGGGGGT	0.622												
GOLGA8DP	100132979	broad.mit.edu	37	15	22709152	22709152	+	Missense_Mutation	SNP	G	G	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr15:22709152G>T	uc010axw.2	-	10	1245	c.347C>A	c.(346-348)gCg>gAg	p.A116E	abParts_uc001yuj.2_Intron|GOLGA8DP_uc010axx.2_Missense_Mutation_p.A116E|DQ588687_uc010tzw.1_5'Flank|DQ582939_uc021sfj.1_5'Flank					Homo sapiens golgin A8 family, member D, pseudogene (GOLGA8DP), non-coding RNA.																		GGCCTGGAGCGCTCCTGCCAC	0.607												
UNC13C	440279	broad.mit.edu	37	15	54542603	54542603	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr15:54542603G>A	uc021smr.1	+	5	3403	c.3403G>A	c.(3403-3405)Gaa>Aaa	p.E1135K	UNC13C_uc021sms.1_Missense_Mutation_p.E1137K	NM_001080534	NP_001074003	Q8NB66	UN13C_HUMAN	Homo sapiens unc-13 homolog C (C. elegans) (UNC13C), mRNA.	1137					exocytosis|intracellular signal transduction	cell junction|cytoplasm|presynaptic membrane	metal ion binding			breast(3)|endometrium(5)|kidney(5)|large_intestine(20)|lung(70)|ovary(6)|pancreas(2)|prostate(2)|upper_aerodigestive_tract(4)|urinary_tract(4)	121				GBM - Glioblastoma multiforme(80;0.0789)|all cancers(107;0.124)		GAAATGCCACGAAAAGTGTCA	0.507												
IGDCC3	9543	broad.mit.edu	37	15	65667680	65667680	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr15:65667680G>A	uc002aos.2	-	1	416	c.164C>T	c.(163-165)cCc>cTc	p.P55L		NM_004884	NP_004875	Q8IVU1	IGDC3_HUMAN	Homo sapiens immunoglobulin superfamily, DCC subclass, member 3 (IGDCC3), mRNA.	55	Ig-like C2-type 1.									breast(1)|endometrium(3)|kidney(3)|large_intestine(7)|lung(9)|ovary(4)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	30						AGGCTGCCCGGGGACGGCAAC	0.582												
LOC645752	645752	broad.mit.edu	37	15	78211648	78211648	+	Missense_Mutation	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr15:78211648A>G	uc010bky.2	-	10	883	c.119T>C	c.(118-120)cTa>cCa	p.L40P						Homo sapiens golgi autoantigen, golgin subfamily a, 6 pseudogene (LOC645752), non-coding RNA.																		CGCCAGGGATAGGGGCTCAGC	0.522												
GOLGA6L10	647042	broad.mit.edu	37	15	83014132	83014132	+	Missense_Mutation	SNP	C	C	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr15:83014132C>G	uc021ssz.1	-	5	551	c.415G>C	c.(415-417)Gag>Cag	p.E139Q	LOC440295_uc002bhl.2_Intron|GOLGA6L9_uc021ssr.1_Intron|LOC440295_uc002bhm.2_Intron|GOLGA6L10_uc021sta.1_Non-coding_Transcript			A6NI86	GG6LA_HUMAN	Homo sapiens golgin A6 family-like 10 (GOLGA6L10), mRNA.	151								p.E151Q(4)		endometrium(1)|kidney(4)	5						GCTGGGGGCTCTGGGGCCAGG	0.522												
GRIN2A	2903	broad.mit.edu	37	16	9857171	9857171	+	Silent	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr16:9857171C>T	uc010uym.2	-	13	4540	c.4230G>A	c.(4228-4230)tcG>tcA	p.S1410S	GRIN2A_uc002czo.4_Silent_p.S1410S|GRIN2A_uc010uyn.2_3'UTR|GRIN2A_uc002czr.4_3'UTR	NM_000833	NP_001127879	Q12879	NMDE1_HUMAN	Homo sapiens glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A), transcript variant 2, mRNA.	1410					response to ethanol	cell junction|N-methyl-D-aspartate selective glutamate receptor complex|outer membrane-bounded periplasmic space|postsynaptic membrane	N-methyl-D-aspartate selective glutamate receptor activity|zinc ion binding			NS(7)|breast(5)|cervix(1)|endometrium(11)|kidney(6)|large_intestine(36)|lung(71)|ovary(4)|prostate(9)|skin(45)|upper_aerodigestive_tract(2)|urinary_tract(1)	198					Felbamate(DB00949)|Glycine(DB00145)|L-Glutamic Acid(DB00142)|Loperamide(DB00836)|Memantine(DB01043)	TGGAACAGTACGATGCCGTTG	0.502												
HYDIN	54768	broad.mit.edu	37	16	70917889	70917889	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr16:70917889C>T	uc002ezr.3	-	58	10061	c.9910G>A	c.(9910-9912)Ggc>Agc	p.G3304S		NM_032821	NP_116210	Q4G0P3	HYDIN_HUMAN	Homo sapiens HYDIN, axonemal central pair apparatus protein (HYDIN), transcript variant 1, mRNA.	3305										breast(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(17)|lung(12)|ovary(2)|skin(3)|stomach(2)|upper_aerodigestive_tract(1)	43		Ovarian(137;0.0654)				GGGTCTCGGCCGGAGATATCG	0.532												
EIF4A1	1973	broad.mit.edu	37	17	7480924	7480924	+	Missense_Mutation	SNP	C	C	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:7480924C>A	uc002gho.2	+	18	3369	c.806C>A	c.(805-807)aCc>aAc	p.T269N	EIF4A1_uc002ghr.1_Missense_Mutation_p.T269N|SNORA67_uc010cml.1_5'Flank|EIF4A1_uc021tpc.1_5'Flank|CD68_uc002ghu.3_5'Flank|CD68_uc002ghv.3_5'Flank	NM_001416	NP_001407	P60842	IF4A1_HUMAN	Homo sapiens eukaryotic translation initiation factor 4A1 (EIF4A1), transcript variant 1, mRNA.	269	Helicase C-terminal.				nuclear-transcribed mRNA poly(A) tail shortening	cytosol|eukaryotic translation initiation factor 4F complex	ATP binding|ATP-dependent helicase activity|mRNA binding|protein binding|RNA cap binding|translation initiation factor activity			NS(1)|breast(2)|cervix(2)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|lung(8)|ovary(2)|prostate(2)|upper_aerodigestive_tract(2)	22						TTGTATGAAACCCTGACCATC	0.537												
PIK3R6	146850	broad.mit.edu	37	17	8741187	8741187	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:8741187G>A	uc002glq.1	-	5	430	c.190_splice	c.e5-1	p.A64_splice	PIK3R6_uc002glr.1_Splice_Site|PIK3R6_uc002gls.1_Splice_Site	NM_001010855	NP_001010855	Q5UE93	PI3R6_HUMAN	Homo sapiens phosphoinositide-3-kinase, regulatory subunit 6 (PIK3R6), mRNA.	64					platelet activation	cytosol											CTGGCTTTCCGCCTGGAAAAC	0.587												
MYH8	4626	broad.mit.edu	37	17	10316043	10316043	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:10316043C>T	uc002gmm.2	-	12	1245	c.1150G>A	c.(1150-1152)Gct>Act	p.A384T	AK097500_uc002gml.1_Intron	NM_002472	NP_002463	P13535	MYH8_HUMAN	Homo sapiens myosin, heavy chain 8, skeletal muscle, perinatal (MYH8), mRNA.	384	Myosin head-like.				muscle filament sliding	cytosol|muscle myosin complex|myofibril|myosin filament	actin binding|ATP binding|calmodulin binding|motor activity|structural constituent of muscle			NS(3)|breast(8)|central_nervous_system(2)|endometrium(11)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(23)|lung(61)|ovary(3)|prostate(3)|skin(10)|upper_aerodigestive_tract(2)|urinary_tract(2)	134						GCCTTGTCAGCGACTGCAGAG	0.423									Trismus-Pseudocamptodactyly Syndrome with Cardiac Myxoma and Freckling			
CPD	1362	broad.mit.edu	37	17	28772878	28772881	+	Frame_Shift_Del	DEL	TTAA	TTAA	-			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:28772878_28772881delTTAA	uc002hfb.2	+	11	2770_2773	c.2713_2716delTTAA	c.(2713-2718)ttaattfs	p.L905fs	CPD_uc010wbo.2_Frame_Shift_Del_p.L658fs|CPD_uc010wbp.2_Non-coding_Transcript	NM_001304	NP_001295	O75976	CBPD_HUMAN	Homo sapiens carboxypeptidase D (CPD), transcript variant 1, mRNA.	905	Carboxypeptidase-like 3.				proteolysis	integral to membrane	metallocarboxypeptidase activity|serine-type carboxypeptidase activity|zinc ion binding			central_nervous_system(1)|endometrium(4)|kidney(1)|large_intestine(9)|liver(1)|lung(13)|skin(5)|stomach(1)|urinary_tract(1)	36						GTTTGAAACTTTAATTAAAGACCT	0.417												
ORMDL3	94103	broad.mit.edu	37	17	38080398	38080398	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:38080398C>T	uc002htj.2	-	1	229	c.59G>A	c.(58-60)cGt>cAt	p.R20H	ORMDL3_uc002hti.1_Non-coding_Transcript|ORMDL3_uc002htk.2_Missense_Mutation_p.R20H	NM_139280	NP_644809	Q8N138	ORML3_HUMAN	Homo sapiens ORM1-like 3 (S. cerevisiae) (ORMDL3), mRNA.	20					ceramide metabolic process	integral to membrane|SPOTS complex	protein binding			endometrium(3)|kidney(1)|lung(1)	5	Colorectal(19;0.000442)		Lung(15;0.0234)			CCAGATGCCACGGCTGTTCAT	0.602												
CNTNAP1	8506	broad.mit.edu	37	17	40837035	40837035	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:40837035G>A	uc002iay.3	+	3	606	c.390G>A	c.(388-390)tcG>tcA	p.S130S	CNTNAP1_uc010wgs.2_Non-coding_Transcript	NM_003632	NP_003623	P78357	CNTP1_HUMAN	Homo sapiens contactin associated protein 1 (CNTNAP1), mRNA.	130	F5/8 type C.				axon guidance|cell adhesion	paranode region of axon	receptor activity|receptor binding|SH3 domain binding|SH3/SH2 adaptor activity			NS(1)|breast(4)|cervix(1)|endometrium(5)|kidney(3)|large_intestine(11)|lung(15)|ovary(5)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	49		Breast(137;0.000143)		BRCA - Breast invasive adenocarcinoma(366;0.143)		TGAACGAGTCGGCGGTGGTGC	0.562												
WIPI1	55062	broad.mit.edu	37	17	66449078	66449078	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:66449078C>T	uc010dey.3	-	1	227	c.136G>A	c.(136-138)Gag>Aag	p.E46K	WIPI1_uc010wqo.2_Intron	NM_017983	NP_060453	Q5MNZ9	WIPI1_HUMAN	Homo sapiens WD repeat domain, phosphoinositide interacting 1 (WIPI1), mRNA.	46					macroautophagy|vesicle targeting, trans-Golgi to endosome	autophagic vacuole membrane|clathrin-coated vesicle|cytosol|endosome membrane|PAS complex|pre-autophagosomal structure membrane|trans-Golgi network	androgen receptor binding|estrogen receptor binding|phosphatidylinositol-3,5-bisphosphate binding|phosphatidylinositol-3-phosphate binding			breast(1)|endometrium(2)|kidney(2)|large_intestine(4)|lung(6)|skin(2)|upper_aerodigestive_tract(1)	18						TCCAGCTGCTCCACAGAACTC	0.488												
GPR142	350383	broad.mit.edu	37	17	72368095	72368095	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr17:72368095G>A	uc021ucp.1	+	3	745	c.736G>A	c.(736-738)Gcc>Acc	p.A246T	GPR142_uc010wqy.2_Missense_Mutation_p.A249T	NM_181790	NP_861455	Q7Z601	GP142_HUMAN	Homo sapiens G protein-coupled receptor 142 (GPR142), mRNA.	249						cell junction|cytoplasm|integral to membrane	G-protein coupled receptor activity			central_nervous_system(1)|endometrium(3)|large_intestine(3)|lung(21)|ovary(2)|prostate(1)|skin(4)	35						AGTCTGGATCGCCATCCTGCT	0.692												
ST8SIA5	29906	broad.mit.edu	37	18	44260035	44260035	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr18:44260035G>A	uc010xcy.1	-	7	1777	c.1209C>T	c.(1207-1209)cgC>cgT	p.R403R	ST8SIA5_uc002lci.1_Silent_p.R214R|ST8SIA5_uc002lcj.1_Silent_p.R367R|ST8SIA5_uc010xcz.1_Silent_p.R336R	NM_013305	NP_037437	O15466	SIA8E_HUMAN	Homo sapiens ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 (ST8SIA5), mRNA.	367					glycosphingolipid biosynthetic process|protein glycosylation	integral to Golgi membrane				kidney(1)|large_intestine(10)|lung(7)|ovary(1)|pancreas(1)|upper_aerodigestive_tract(2)	22						CCGTGTGCACGCGGAGGATGC	0.652												
CDH7	1005	broad.mit.edu	37	18	63430143	63430143	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr18:63430143C>T	uc002lkb.3	+	1	491	c.65C>T	c.(64-66)tCt>tTt	p.S22F	CDH7_uc002ljz.3_Missense_Mutation_p.S22F|CDH7_uc002lka.3_Missense_Mutation_p.S22F	NM_004361	NP_387450	Q9ULB5	CADH7_HUMAN	Homo sapiens cadherin 7, type 2 (CDH7), transcript variant b, mRNA.	22					adherens junction organization|cell junction assembly|homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			NS(1)|breast(1)|cervix(1)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(4)|lung(43)|ovary(3)|pancreas(1)|prostate(1)|skin(7)|stomach(1)|upper_aerodigestive_tract(2)	80		Esophageal squamous(42;0.129)				CTGTGTTTTTCTGGGATGAGT	0.433												
RPSA	388524	broad.mit.edu	37	19	24010294	24010294	+	Missense_Mutation	SNP	C	C	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr19:24010294C>G	uc002nrn.3	+	3	754	c.331C>G	c.(331-333)Cag>Gag	p.Q111E		NM_002295	NP_002286	P08865	RSSA_HUMAN	Homo sapiens ribosomal protein SA (RPSA), transcript variant 1, mRNA.	111	Interaction with PPP1R16B.				cell adhesion|endocrine pancreas development|endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)|endonucleolytic cleavage to generate mature 3'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA)|ribosomal small subunit assembly|rRNA export from nucleus|translational elongation|translational termination|viral transcription	90S preribosome|cytosolic small ribosomal subunit|nucleus|plasma membrane	protein binding|receptor activity|ribosome binding|structural constituent of ribosome	p.Q111E(12)		endometrium(1)|large_intestine(1)|lung(3)|prostate(1)|upper_aerodigestive_tract(1)	7				KIRC - Kidney renal clear cell carcinoma(284;0.0509)|Kidney(284;0.064)		CTTCACTAACCAGATCCAGGC	0.567												
CD3EAP	10849	broad.mit.edu	37	19	45911859	45911861	+	In_Frame_Del	DEL	GAA	GAA	-			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr19:45911859_45911861delGAA	uc002pbr.1	+	2	645_647	c.639_641delGAA	c.(637-642)cggaag>cgg	p.K219del	PPP1R13L_uc002pbo.3_5'Flank|PPP1R13L_uc002pbp.2_5'Flank|CD3EAP_uc002pbq.1_In_Frame_Del_p.K217del|ERCC1_uc002pbt.2_3'UTR|ERCC1_uc002pbs.2_3'UTR|ERCC1_uc002pbu.2_3'UTR	NM_012099	NP_036231	O15446	RPA34_HUMAN	Homo sapiens CD3e molecule, epsilon associated protein (CD3EAP), mRNA.	217					rRNA transcription|transmembrane receptor protein tyrosine kinase signaling pathway	chromosome|RNA polymerase I transcription factor complex	DNA-directed RNA polymerase activity	p.N218fs*58(2)		breast(2)|endometrium(1)|large_intestine(3)|lung(2)|ovary(2)|prostate(1)	11		all_neural(266;0.224)|Ovarian(192;0.231)		OV - Ovarian serous cystadenocarcinoma(262;0.0251)		TGGATGTGCGGAAGAAGAAGAAG	0.581												
KLK15	55554	broad.mit.edu	37	19	51330305	51330305	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr19:51330305G>A	uc002ptl.3	-	2	341	c.310C>T	c.(310-312)Cgc>Tgc	p.R104C	KLK15_uc002ptm.3_Missense_Mutation_p.R104C|KLK15_uc002ptn.3_Missense_Mutation_p.R104C|KLK15_uc002pto.3_Missense_Mutation_p.R103C|KLK15_uc010ych.2_Non-coding_Transcript|KLK15_uc010yci.2_Missense_Mutation_p.R103C|KLK15_uc010eod.3_Non-coding_Transcript	NM_017509	NP_059979	Q9H2R5	KLK15_HUMAN	Homo sapiens kallikrein-related peptidase 15 (KLK15), transcript variant 4, mRNA.	104	Peptidase S1.				proteolysis	extracellular region	serine-type endopeptidase activity			breast(1)|endometrium(2)|large_intestine(5)|liver(1)|lung(12)|skin(2)|upper_aerodigestive_tract(1)	24		all_neural(266;0.057)		OV - Ovarian serous cystadenocarcinoma(262;0.00758)|GBM - Glioblastoma multiforme(134;0.0143)		ATGTCGTTGCGGTGGCTGCGC	0.697												
NLRP5	126206	broad.mit.edu	37	19	56539657	56539657	+	Silent	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr19:56539657C>T	uc002qmj.3	+	6	2058	c.2058C>T	c.(2056-2058)gaC>gaT	p.D686D	NLRP5_uc002qmi.3_Silent_p.D667D	NM_153447	NP_703148	P59047	NALP5_HUMAN	Homo sapiens NLR family, pyrin domain containing 5 (NLRP5), mRNA.	686						mitochondrion|nucleolus	ATP binding			breast(1)|central_nervous_system(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(8)|ovary(5)|skin(2)|stomach(4)|upper_aerodigestive_tract(2)	25		Colorectal(82;3.46e-05)|Ovarian(87;0.0481)|Renal(1328;0.157)		GBM - Glioblastoma multiforme(193;0.0326)		ACACCCTGGACGCCTTCCACT	0.542												
APOB	338	broad.mit.edu	37	2	21230333	21230333	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:21230333C>T	uc002red.3	-	25	9535	c.9407G>A	c.(9406-9408)cGt>cAt	p.R3136H		NM_000384	NP_000375	P04114	APOB_HUMAN	Homo sapiens apolipoprotein B (including Ag(x) antigen) (APOB), mRNA.	3136					cholesterol homeostasis|cholesterol metabolic process|leukocyte migration|low-density lipoprotein particle clearance|low-density lipoprotein particle remodeling|platelet activation|positive regulation of cholesterol storage|positive regulation of macrophage derived foam cell differentiation|receptor-mediated endocytosis|response to virus	chylomicron remnant|clathrin-coated endocytic vesicle membrane|endoplasmic reticulum lumen|endoplasmic reticulum membrane|endosome lumen|endosome membrane|intermediate-density lipoprotein particle|low-density lipoprotein particle|mature chylomicron|microsome|plasma membrane|very-low-density lipoprotein particle	cholesterol transporter activity|enzyme binding|heparin binding|low-density lipoprotein particle receptor binding|phospholipid binding|protein heterodimerization activity	p.R3136H(2)|p.R3136C(2)		NS(5)|autonomic_ganglia(1)|breast(6)|central_nervous_system(4)|cervix(3)|endometrium(19)|kidney(10)|large_intestine(63)|liver(5)|lung(125)|ovary(16)|pancreas(1)|prostate(5)|skin(31)|stomach(1)|upper_aerodigestive_tract(4)|urinary_tract(6)	305	Acute lymphoblastic leukemia(172;0.155)|all_hematologic(175;0.215)				Atorvastatin(DB01076)	GTAAGGTAGACGCATTTCAGG	0.373												
NRXN1	9378	broad.mit.edu	37	2	50573861	50573861	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:50573861T>C	uc021vhh.1	-						NRXN1_uc010fbp.3_Missense_Mutation_p.Y76C|NRXN1_uc002rxb.4_Intron|NRXN1_uc021vhg.1_Intron|NRXN1_uc021vhi.1_Intron|NRXN1_uc021vhj.1_Intron|NRXN1_uc002rxc.1_Intron	NM_004801	NP_004792	Q9ULB1	NRX1A_HUMAN	Homo sapiens neurexin 1 (NRXN1), transcript variant alpha1, mRNA.						adult behavior|axon guidance|cell adhesion|grooming behavior|learning|neuromuscular process controlling balance|positive regulation of excitatory postsynaptic membrane potential|prepulse inhibition	cell surface|integral to plasma membrane	metal ion binding|protein binding|receptor activity			breast(1)|endometrium(3)|kidney(3)|large_intestine(10)|lung(33)|ovary(3)|prostate(1)|skin(2)|upper_aerodigestive_tract(2)	58		all_hematologic(82;0.152)|Acute lymphoblastic leukemia(82;0.192)	Lung(47;0.0813)|LUSC - Lung squamous cell carcinoma(58;0.116)			CGGTGACCTGTAGATTGCAAT	0.602												
Unknown	388955	broad.mit.edu	37	2	63849736	63849736	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:63849736G>A								MDH1 (15406 upstream) : UGP2 (218362 downstream)																							GATGTACACCGAGTGAGCAAC	0.552												
ETAA1	54465	broad.mit.edu	37	2	67631223	67631226	+	Frame_Shift_Del	DEL	CAAA	CAAA	-			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:67631223_67631226delCAAA	uc002sdz.1	+	4	1548_1551	c.1409_1412delCAAA	c.(1408-1413)tcaaacfs	p.S470fs		NM_019002	NP_061875	Q9NY74	ETAA1_HUMAN	Homo sapiens Ewing tumor-associated antigen 1 (ETAA1), mRNA.	470						cytoplasm|nucleus				autonomic_ganglia(1)|breast(1)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(10)|lung(9)|ovary(3)|prostate(1)|stomach(3)|urinary_tract(1)	33						TCAAATAAATCAAACAAATTATCC	0.265												
SLC9A4	389015	broad.mit.edu	37	2	103141552	103141552	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:103141552C>T	uc002tbz.4	+	9	2345	c.1888C>T	c.(1888-1890)Cgc>Tgc	p.R630C		NM_001011552	NP_001011552	Q6AI14	SL9A4_HUMAN	Homo sapiens solute carrier family 9 (sodium/hydrogen exchanger), member 4 (SLC9A4), mRNA.	630					regulation of pH	apical plasma membrane|basolateral plasma membrane|integral to membrane	sodium:hydrogen antiporter activity			NS(1)|autonomic_ganglia(1)|central_nervous_system(1)|cervix(2)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(8)|lung(16)|ovary(1)|skin(4)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	43						GATTCTGATCCGCCGCCAGAA	0.502												
LY75-CD302	4065	broad.mit.edu	37	2	160711043	160711043	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr2:160711043C>T	uc002ubb.4	-	17	2497	c.2423G>A	c.(2422-2424)cGt>cAt	p.R808H	LY75-CD302_uc010fos.3_Missense_Mutation_p.R808H|LY75-CD302_uc002ubc.4_Missense_Mutation_p.R808H	NM_001198759	NP_001185688	O60449	LY75_HUMAN	Homo sapiens LY75-CD302 readthrough (LY75-CD302), transcript variant 1, mRNA.	808					endocytosis|immune response|inflammatory response	integral to plasma membrane	receptor activity|sugar binding	p.R808H(1)									AATTCCAGCACGGTCTAAAGA	0.363												
TGM3	7053	broad.mit.edu	37	20	2312692	2312692	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr20:2312692C>T	uc002wfx.4	+	9	1475	c.1378C>T	c.(1378-1380)Ctt>Ttt	p.L460F		NM_003245	NP_003236	Q08188	TGM3_HUMAN	Homo sapiens transglutaminase 3 (E polypeptide, protein-glutamine-gamma-glutamyltransferase) (TGM3), mRNA.	460					cell envelope organization|hair follicle morphogenesis|keratinization|peptide cross-linking|protein tetramerization	cytoplasm|extrinsic to internal side of plasma membrane	acyltransferase activity|calcium ion binding|GDP binding|GTP binding|GTPase activity|magnesium ion binding|protein-glutamine gamma-glutamyltransferase activity			breast(3)|cervix(1)|endometrium(1)|kidney(4)|large_intestine(11)|lung(10)|ovary(3)|pancreas(1)|prostate(1)|skin(2)|urinary_tract(2)	39					L-Glutamine(DB00130)	TTTGGGGAAACTTAAACCCAA	0.522												
RPRD1B	58490	broad.mit.edu	37	20	36687859	36687859	+	Nonsense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr20:36687859C>T	uc002xho.4	+	4	994	c.592C>T	c.(592-594)Cga>Tga	p.R198*		NM_021215	NP_067038	Q9NQG5	RPR1B_HUMAN	Homo sapiens regulation of nuclear pre-mRNA domain containing 1B (RPRD1B), mRNA.	198										endometrium(3)|kidney(1)|large_intestine(2)|lung(4)|pancreas(1)|skin(1)	12						TGCTACTGTCCGACAGAAAAT	0.433												
LBP	3929	broad.mit.edu	37	20	36995435	36995435	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr20:36995435G>A	uc002xic.1	+	8	979	c.944G>A	c.(943-945)cGa>cAa	p.R315Q		NM_004139	NP_004130	P18428	LBP_HUMAN	Homo sapiens lipopolysaccharide binding protein (LBP), mRNA.	315					acute-phase response|cellular defense response|cellular response to lipoteichoic acid|defense response to Gram-negative bacterium|defense response to Gram-positive bacterium|detection of molecule of bacterial origin|innate immune response|lipid transport|lipopolysaccharide transport|lipopolysaccharide-mediated signaling pathway|macrophage activation involved in immune response|negative regulation of tumor necrosis factor production|opsonization|positive regulation of interleukin-6 production|positive regulation of interleukin-8 production|positive regulation of macrophage activation|positive regulation of respiratory burst involved in inflammatory response|positive regulation of toll-like receptor 4 signaling pathway|positive regulation of tumor necrosis factor production|Toll signaling pathway	extracellular space	Gram-negative bacterial cell surface binding|Gram-positive bacterial cell surface binding|lipid binding|lipopolysaccharide binding|lipoteichoic acid binding|receptor binding			central_nervous_system(1)|endometrium(3)|kidney(2)|large_intestine(2)|lung(16)|ovary(2)|prostate(1)|urinary_tract(1)	28		Myeloproliferative disorder(115;0.00878)				TCTAATATCCGACTGACCACC	0.537												
CHD6	84181	broad.mit.edu	37	20	40065924	40065924	+	Missense_Mutation	SNP	T	T	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr20:40065924T>G	uc002xka.1	-	26	4236	c.4058A>C	c.(4057-4059)cAg>cCg	p.Q1353P	CHD6_uc002xkb.1_Missense_Mutation_p.Q119P	NM_032221	NP_115597	Q8TD26	CHD6_HUMAN	Homo sapiens chromodomain helicase DNA binding protein 6 (CHD6), mRNA.	1353					chromatin remodeling|nervous system development|regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	ATP binding|ATP-dependent helicase activity|chromatin binding|DNA binding			breast(8)|central_nervous_system(2)|cervix(2)|endometrium(5)|kidney(4)|large_intestine(24)|lung(53)|ovary(8)|prostate(5)|skin(8)|stomach(1)|urinary_tract(9)	129		Myeloproliferative disorder(115;0.00425)				CGTTTGTTTCTGGAGGCCATC	0.398												
KCNB1	3745	broad.mit.edu	37	20	48098620	48098620	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr20:48098620C>T	uc002xur.1	-	0	564	c.398G>A	c.(397-399)tGc>tAc	p.C133Y	KCNB1_uc002xus.1_Missense_Mutation_p.C133Y	NM_004975	NP_004966	Q14721	KCNB1_HUMAN	Homo sapiens potassium voltage-gated channel, Shab-related subfamily, member 1 (KCNB1), mRNA.	133					energy reserve metabolic process|regulation of insulin secretion	voltage-gated potassium channel complex	protein binding|voltage-gated potassium channel activity			central_nervous_system(1)|endometrium(4)|kidney(2)|large_intestine(8)|liver(1)|lung(22)|pancreas(2)|prostate(7)|skin(4)|stomach(1)|urinary_tract(1)	53			BRCA - Breast invasive adenocarcinoma(12;0.000405)|COAD - Colon adenocarcinoma(4;0.14)|Colorectal(8;0.166)			GCGGGCCTGGCAGCAGGACTC	0.607												
KRTAP20-2	337976	broad.mit.edu	37	21	32007616	32007616	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr21:32007616C>T	uc011adg.2	+	0	34	c.34C>T	c.(34-36)Cgt>Tgt	p.R12C		NM_181616	NP_853647	Q3LI61	KR202_HUMAN	Homo sapiens keratin associated protein 20-2 (KRTAP20-2), mRNA.	12						intermediate filament				central_nervous_system(1)|endometrium(3)|kidney(1)|lung(2)|ovary(1)	8						TGGTGGTCTGCGTTATGGCTA	0.517												
POTEH	23784	broad.mit.edu	37	22	16279238	16279238	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr22:16279238T>C	uc010gqp.2	-	3	1037	c.985A>G	c.(985-987)Atc>Gtc	p.I329V	POTEH_uc002zlg.1_Non-coding_Transcript|POTEH_uc002zlh.1_Missense_Mutation_p.I48V|POTEH_uc002zlj.1_Missense_Mutation_p.I164V	NM_001136213	NP_001129685	Q6S545	POTEH_HUMAN	Homo sapiens POTE ankyrin domain family, member H (POTEH), mRNA.	329										NS(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(2)|kidney(1)|lung(20)|ovary(1)|skin(7)|urinary_tract(2)	37						TTTTTCTTGATTAAAAATTTC	0.338												
PRODH	5625	broad.mit.edu	37	22	18912582	18912582	+	Missense_Mutation	SNP	G	G	A	rs147270439		TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr22:18912582G>A	uc002zok.4	-	4	853	c.649C>T	c.(649-651)Cgc>Tgc	p.R217C	PRODH_uc002zoj.4_Missense_Mutation_p.R107C|PRODH_uc002zol.4_Missense_Mutation_p.R109C	NM_016335	NP_057419	O43272	PROD_HUMAN	Homo sapiens proline dehydrogenase (oxidase) 1 (PRODH), nuclear gene encoding mitochondrial protein, transcript variant 1, mRNA.	217					glutamate biosynthetic process|induction of apoptosis by oxidative stress|proline catabolic process	mitochondrial inner membrane|mitochondrial matrix	proline dehydrogenase activity			breast(1)|endometrium(3)|lung(4)|upper_aerodigestive_tract(1)	9					L-Proline(DB00172)	TCGATGCAGCGCAAGAATGTC	0.632												
MAPK1	5594	broad.mit.edu	37	22	22142632	22142632	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr22:22142632T>C	uc002zvn.3	-	5	1010	c.770A>G	c.(769-771)aAt>aGt	p.N257S	MAPK1_uc002zvo.3_Missense_Mutation_p.N257S|MAPK1_uc010gtk.1_Intron	NM_002745	NP_620407	P28482	MK01_HUMAN	Homo sapiens mitogen-activated protein kinase 1 (MAPK1), transcript variant 1, mRNA.	257	Protein kinase.				activation of MAPK activity|activation of MAPKK activity|axon guidance|cell cycle|epidermal growth factor receptor signaling pathway|ERK1 and ERK2 cascade|induction of apoptosis|innate immune response|insulin receptor signaling pathway|interspecies interaction between organisms|MyD88-dependent toll-like receptor signaling pathway|MyD88-independent toll-like receptor signaling pathway|nerve growth factor receptor signaling pathway|platelet activation|Ras protein signal transduction|regulation of sequence-specific DNA binding transcription factor activity|stress-activated MAPK cascade|synaptic transmission|Toll signaling pathway|toll-like receptor 1 signaling pathway|toll-like receptor 2 signaling pathway|toll-like receptor 3 signaling pathway|toll-like receptor 4 signaling pathway|transcription, DNA-dependent	cytosol|nucleoplasm	ATP binding|DNA binding|MAP kinase activity|phosphatase binding|RNA polymerase II carboxy-terminal domain kinase activity			NS(1)|breast(1)|central_nervous_system(1)|cervix(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(2)|lung(2)|ovary(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	17	Colorectal(54;0.105)	all_lung(157;3.89e-05)		READ - Rectum adenocarcinoma(21;0.0689)	Arsenic trioxide(DB01169)	AGCTTTTAAATTTATTATACA	0.353												
TMPRSS6	164656	broad.mit.edu	37	22	37470715	37470715	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr22:37470715C>T	uc003aqt.1	-	11	1438	c.1376G>A	c.(1375-1377)gGa>gAa	p.G459E	TMPRSS6_uc003aqs.1_Missense_Mutation_p.G468E	NM_153609	NP_705837	Q8IU80	TMPS6_HUMAN	Homo sapiens transmembrane protease, serine 6 (TMPRSS6), mRNA.	468	LDL-receptor class A 1.				angiogenesis|extracellular matrix organization|fibrinolysis|intracellular signal transduction|proteolysis	integral to membrane|intracellular|plasma membrane	serine-type endopeptidase activity			breast(5)|central_nervous_system(4)|endometrium(4)|kidney(4)|large_intestine(3)|lung(13)|ovary(1)|prostate(1)|skin(2)|stomach(3)	40						GACACAGAGTCCATTCACAGA	0.632												
TRANK1	9881	broad.mit.edu	37	3	36898731	36898731	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:36898731C>T	uc003cgj.3	-	11	2598	c.2350G>A	c.(2350-2352)Gac>Aac	p.D784N		NM_014831	NP_055646	O15050	TRNK1_HUMAN	Homo sapiens tetratricopeptide repeat and ankyrin repeat containing 1 (TRANK1), mRNA.	784					DNA repair		ATP binding|ATP-dependent DNA helicase activity|DNA binding			NS(2)|autonomic_ganglia(1)|breast(1)|central_nervous_system(1)|cervix(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(18)|lung(20)|ovary(1)|prostate(3)|skin(6)|upper_aerodigestive_tract(1)|urinary_tract(2)	73						TTATCGAAGTCCTGGAGGCAG	0.502												
CEP97	79598	broad.mit.edu	37	3	101451368	101451368	+	Missense_Mutation	SNP	T	T	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:101451368T>G	uc003dvk.1	+	5	625	c.598T>G	c.(598-600)Ttg>Gtg	p.L200V	CEP97_uc010hpm.1_Missense_Mutation_p.L166V|CEP97_uc011bhf.1_Missense_Mutation_p.L200V|CEP97_uc003dvl.1_5'UTR|CEP97_uc003dvm.1_Missense_Mutation_p.L38V	NM_024548	NP_078824	Q8IW35	CEP97_HUMAN	Homo sapiens centrosomal protein 97kDa (CEP97), mRNA.	200						centrosome|nucleus	protein binding			cervix(1)|endometrium(2)|kidney(4)|large_intestine(4)|lung(13)|ovary(2)|prostate(1)|skin(1)|urinary_tract(1)	29						ATTGGAACAGTTGTCGATTAT	0.418												
TMPRSS7	344805	broad.mit.edu	37	3	111799811	111799811	+	Missense_Mutation	SNP	G	G	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:111799811G>T	uc010hqb.2	+	15	2204	c.2034G>T	c.(2032-2034)tgG>tgT	p.W678C	TMPRSS7_uc011bhr.1_Missense_Mutation_p.W533C	NM_001042575	NP_001036040	Q7RTY8	TMPS7_HUMAN	Homo sapiens transmembrane protease, serine 7 (TMPRSS7), transcript variant 1, mRNA.	804	Peptidase S1.				proteolysis	integral to membrane|plasma membrane	serine-type endopeptidase activity			breast(2)|endometrium(6)|kidney(2)|large_intestine(4)|lung(11)|ovary(2)|prostate(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(3)|urinary_tract(1)	34						ATGGAAAATGGATTTTGACTG	0.403												
MECOM	2122	broad.mit.edu	37	3	168849257	168849257	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:168849257G>A	uc011bpj.1	-	3	976	c.573C>T	c.(571-573)agC>agT	p.S191S	MECOM_uc010hwk.1_Silent_p.S26S|MECOM_uc003ffj.3_Silent_p.S67S|MECOM_uc003ffi.3_Silent_p.S3S|MECOM_uc011bpi.1_Silent_p.S3S|MECOM_uc003ffn.3_Silent_p.S3S|MECOM_uc003ffk.2_Silent_p.S3S|MECOM_uc003ffl.2_Silent_p.S163S|MECOM_uc011bpk.1_Silent_p.S3S|MECOM_uc010hwn.2_Silent_p.S191S|MECOM_uc003ffm.1_Silent_p.S67S	NM_004991	NP_004982	Q13465	MDS1_HUMAN	Homo sapiens MDS1 and EVI1 complex locus (MECOM), transcript variant 4, mRNA.	98							sequence-specific DNA binding transcription factor activity	p.C190G(1)		NS(1)|breast(4)|central_nervous_system(1)|endometrium(9)|kidney(4)|large_intestine(13)|liver(1)|lung(28)|ovary(2)|pancreas(1)|prostate(2)|skin(12)|stomach(1)|upper_aerodigestive_tract(2)|urinary_tract(4)	85						GATAGTCTTCGCTCTTCATGA	0.458												
PIK3CA	5290	broad.mit.edu	37	3	178916854	178916854	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:178916854G>A	uc003fjk.3	+	1	398	c.241G>A	c.(241-243)Gaa>Aaa	p.E81K		NM_006218	NP_006209	P42336	PK3CA_HUMAN	Homo sapiens phosphoinositide-3-kinase, catalytic, alpha polypeptide (PIK3CA), mRNA.	81	PI3K-ABD.				epidermal growth factor receptor signaling pathway|fibroblast growth factor receptor signaling pathway|insulin receptor signaling pathway|leukocyte migration|nerve growth factor receptor signaling pathway|phosphatidylinositol-mediated signaling|platelet activation|T cell costimulation|T cell receptor signaling pathway		1-phosphatidylinositol-3-kinase activity|ATP binding|phosphatidylinositol-4,5-bisphosphate 3-kinase activity	p.E81K(18)|p.E80K(1)		NS(16)|autonomic_ganglia(4)|biliary_tract(22)|bone(1)|breast(2150)|central_nervous_system(110)|cervix(33)|endometrium(473)|eye(1)|haematopoietic_and_lymphoid_tissue(35)|kidney(14)|large_intestine(1202)|liver(42)|lung(202)|meninges(1)|oesophagus(28)|ovary(235)|pancreas(17)|penis(8)|pituitary(12)|prostate(10)|skin(155)|small_intestine(1)|soft_tissue(18)|stomach(121)|thyroid(80)|upper_aerodigestive_tract(70)|urinary_tract(208)	5269	all_cancers(143;1.19e-17)|Ovarian(172;0.00769)|Breast(254;0.155)		OV - Ovarian serous cystadenocarcinoma(80;9.59e-28)|GBM - Glioblastoma multiforme(14;0.003)|BRCA - Breast invasive adenocarcinoma(182;0.0282)			AGAAAGGGAAGAATTTTTTGA	0.358		57	Mis		"""colorectal, gastric, gliobastoma, breast"""					HNSCC(19;0.045)|TSP Lung(28;0.18)		
LAMP3	27074	broad.mit.edu	37	3	182870190	182870190	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:182870190G>A	uc003flh.4	-	2	1085	c.861C>T	c.(859-861)ggC>ggT	p.G287G		NM_014398	NP_055213	Q9UQV4	LAMP3_HUMAN	Homo sapiens lysosomal-associated membrane protein 3 (LAMP3), mRNA.	287					cell proliferation	integral to membrane|lysosomal membrane				breast(1)|central_nervous_system(1)|cervix(1)|endometrium(2)|kidney(4)|large_intestine(6)|lung(9)|ovary(2)|prostate(2)	28	all_cancers(143;9.14e-14)|Ovarian(172;0.0355)		all cancers(12;2.91e-44)|Epithelial(37;5.52e-38)|LUSC - Lung squamous cell carcinoma(7;7.12e-25)|Lung(8;6.39e-23)|OV - Ovarian serous cystadenocarcinoma(80;4.16e-21)			TCACAAATCCGCCCTGAAAAT	0.512												
LSG1	55341	broad.mit.edu	37	3	194373563	194373563	+	Silent	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr3:194373563C>T	uc003fui.3	-	7	1383	c.1068G>A	c.(1066-1068)caG>caA	p.Q356Q		NM_018385	NP_060855	Q9H089	LSG1_HUMAN	Homo sapiens large subunit GTPase 1 homolog (S. cerevisiae) (LSG1), mRNA.	356					nuclear export|protein transport	Cajal body|endoplasmic reticulum	GTP binding|hydrolase activity			breast(2)|endometrium(3)|large_intestine(2)|lung(9)	16	all_cancers(143;1.68e-08)|Ovarian(172;0.0634)		OV - Ovarian serous cystadenocarcinoma(49;4.34e-18)|LUSC - Lung squamous cell carcinoma(58;3.55e-06)|Lung(62;4.19e-06)	GBM - Glioblastoma multiforme(46;7.55e-06)		AATTGTGTATCTGCCTCTTCT	0.507												
PCDH7	5099	broad.mit.edu	37	4	30725808	30725808	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:30725808T>C	uc003gsk.1	+	0	3772	c.2764T>C	c.(2764-2766)Ttt>Ctt	p.F922L	PCDH7_uc011bxx.2_Missense_Mutation_p.F922L|PCDH7_uc021xnd.1_Missense_Mutation_p.F922L|PCDH7_uc021xnc.1_Missense_Mutation_p.F922L	NM_002589	NP_002580	O60245	PCDH7_HUMAN	Homo sapiens protocadherin 7 (PCDH7), transcript variant a, mRNA.	922					homophilic cell adhesion	integral to plasma membrane	calcium ion binding			NS(1)|breast(2)|endometrium(1)|haematopoietic_and_lymphoid_tissue(2)|kidney(5)|large_intestine(8)|liver(1)|lung(26)|ovary(2)|prostate(2)|skin(3)|upper_aerodigestive_tract(2)	55						TCACGAAGACTTTTTTACACC	0.383												
SMR3A	10879	broad.mit.edu	37	4	71255518	71255518	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:71255518G>A	uc011cas.2	+	2	274	c.193G>A	c.(193-195)Gca>Aca	p.A65T	SMR3A_uc003hfh.3_Missense_Mutation_p.A65T	NM_006685	NP_006676	Q99954	SMR3A_HUMAN	Homo sapiens submaxillary gland androgen regulated protein 3B (SMR3B), mRNA.	69	Pro-rich.					extracellular region				endometrium(1)|large_intestine(1)|lung(7)|ovary(1)|prostate(1)|skin(4)	15		all_hematologic(202;0.196)				TCCTCCTCCCGCACCCTATGG	0.602												
AFM	173	broad.mit.edu	37	4	74364954	74364954	+	Silent	SNP	T	T	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:74364954T>A	uc003hhb.3	+	10	1444	c.1413T>A	c.(1411-1413)gtT>gtA	p.V471V		NM_001133	NP_001124	P43652	AFAM_HUMAN	Homo sapiens afamin (AFM), mRNA.	471	Albumin 3.				vitamin transport		vitamin E binding			breast(2)|central_nervous_system(2)|endometrium(2)|kidney(1)|large_intestine(8)|lung(9)|ovary(2)|skin(2)|upper_aerodigestive_tract(2)|urinary_tract(2)	32	Breast(15;0.00102)		Epithelial(6;5.69e-05)|OV - Ovarian serous cystadenocarcinoma(6;0.000324)|all cancers(17;0.000555)|Lung(101;0.103)|LUSC - Lung squamous cell carcinoma(112;0.154)			TTGCCTGTGTTGATAATTTGG	0.388												
KLHL8	57563	broad.mit.edu	37	4	88091238	88091238	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:88091238G>A	uc011cdb.1	-	7	1915	c.1530C>T	c.(1528-1530)taC>taT	p.Y510Y	KLHL8_uc003hql.1_Silent_p.Y510Y|KLHL8_uc003hqm.1_Silent_p.Y434Y|KLHL8_uc003hqn.1_Silent_p.Y327Y|KLHL8_uc010ikj.1_Silent_p.Y159Y	NM_020803	NP_065854	Q9P2G9	KLHL8_HUMAN	Homo sapiens kelch-like 8 (Drosophila) (KLHL8), mRNA.	510										breast(1)|endometrium(5)|kidney(1)|large_intestine(3)|lung(5)|stomach(1)|upper_aerodigestive_tract(1)	17		Hepatocellular(203;0.114)|all_hematologic(202;0.21)|Acute lymphoblastic leukemia(40;0.242)		OV - Ovarian serous cystadenocarcinoma(123;0.000603)		CACCAACTACGTATAAGCAAC	0.358												
ADH1A	124	broad.mit.edu	37	4	100208729	100208729	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:100208729G>A	uc003hur.2	-	1	226	c.112C>T	c.(112-114)Cgt>Tgt	p.R38C	LOC100507053_uc003hum.2_Intron|ADH1A_uc010ilf.1_5'Flank|ADH1A_uc010ilg.2_Missense_Mutation_p.R38C	NM_000667	NP_000658	P07327	ADH1A_HUMAN	Homo sapiens alcohol dehydrogenase 1A (class I), alpha polypeptide (ADH1A), mRNA.	38					ethanol oxidation|transcription, DNA-dependent|xenobiotic metabolic process	cytosol	alcohol dehydrogenase activity, zinc-dependent|protein binding|zinc ion binding			endometrium(2)|kidney(2)|large_intestine(3)|lung(11)|ovary(1)|prostate(1)|skin(4)|stomach(1)	25				OV - Ovarian serous cystadenocarcinoma(123;9.56e-08)	Fomepizole(DB01213)|NADH(DB00157)	ACCTTAATACGAACTTCATGG	0.348												
DCHS2	54798	broad.mit.edu	37	4	155241881	155241881	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:155241881G>A	uc003inw.2	-	13	3305	c.3305C>T	c.(3304-3306)aCg>aTg	p.T1102M		NM_017639	NP_060109	Q6V1P9	PCD23_HUMAN	Homo sapiens dachsous 2 (Drosophila) (DCHS2), transcript variant 1, mRNA.	1102	Cadherin 9.				homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			NS(1)|breast(2)|central_nervous_system(1)|cervix(3)|endometrium(8)|kidney(5)|large_intestine(54)|lung(63)|ovary(4)|pancreas(1)|prostate(14)|skin(12)|stomach(4)|upper_aerodigestive_tract(2)|urinary_tract(2)	176	all_hematologic(180;0.208)	Renal(120;0.0854)		LUSC - Lung squamous cell carcinoma(193;0.107)		AAATGGATTCGTGCCAGGGTT	0.453												
TLL1	7092	broad.mit.edu	37	4	166964454	166964454	+	Silent	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:166964454T>C	uc003irh.2	+	11	2054	c.1407T>C	c.(1405-1407)aaT>aaC	p.N469N	TLL1_uc011cjn.2_Silent_p.N469N|TLL1_uc011cjo.2_Silent_p.N293N	NM_012464	NP_036596	O43897	TLL1_HUMAN	Homo sapiens tolloid-like 1 (TLL1), transcript variant 1, mRNA.	469	CUB 2.				cell differentiation|proteolysis|skeletal system development	extracellular region	calcium ion binding|metalloendopeptidase activity|zinc ion binding			NS(1)|breast(1)|central_nervous_system(1)|endometrium(7)|kidney(4)|large_intestine(21)|lung(26)|ovary(2)|prostate(5)|skin(6)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	77	all_hematologic(180;0.221)	Melanoma(52;0.0315)|Prostate(90;0.0405)		GBM - Glioblastoma multiforme(119;0.103)		TACGTAAAAATGAAGGACAGA	0.408												
GALNT7	51809	broad.mit.edu	37	4	174235303	174235303	+	Frame_Shift_Del	DEL	A	A	-			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr4:174235303delA	uc003isz.4	+	8	1667	c.1584delA	c.(1582-1584)ccafs	p.P528fs	GALNT7_uc011ckb.2_Frame_Shift_Del_p.P305fs	NM_017423	NP_059119	Q86SF2	GALT7_HUMAN	Homo sapiens UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 7 (GalNAc-T7) (GALNT7), mRNA.	528					protein O-linked glycosylation	Golgi membrane|integral to membrane	polypeptide N-acetylgalactosaminyltransferase activity|sugar binding			central_nervous_system(1)|kidney(3)|large_intestine(5)|liver(1)|lung(9)	19		Prostate(90;0.0132)|Renal(120;0.0183)|Melanoma(52;0.0749)|all_hematologic(60;0.107)|all_neural(102;0.122)		all cancers(43;1.87e-18)|Epithelial(43;3.44e-17)|OV - Ovarian serous cystadenocarcinoma(60;2.48e-09)|STAD - Stomach adenocarcinoma(60;0.0019)|GBM - Glioblastoma multiforme(59;0.0119)|LUSC - Lung squamous cell carcinoma(193;0.0199)		ACCCTTTGCCACCCAAAAATG	0.393												
ANKRD55	79722	broad.mit.edu	37	5	55407551	55407551	+	Missense_Mutation	SNP	G	G	A	rs147414262	byFrequency	TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:55407551G>A	uc003jqu.3	-	9	1176	c.1024C>T	c.(1024-1026)Cgg>Tgg	p.R342W	ANKRD55_uc003jqt.3_Missense_Mutation_p.R54W	NM_024669	NP_078945	Q3KP44	ANR55_HUMAN	Homo sapiens ankyrin repeat domain 55 (ANKRD55), mRNA.	341										breast(1)|central_nervous_system(1)|endometrium(1)|kidney(2)|large_intestine(7)|lung(17)|ovary(1)|prostate(1)|skin(2)|stomach(1)	34		Lung NSC(810;8.69e-05)|Prostate(74;0.00634)|Breast(144;0.0334)|Ovarian(174;0.223)				ACGTTGAACCGTCTCTCCTTC	0.512												
FBN2	2201	broad.mit.edu	37	5	127729056	127729056	+	Missense_Mutation	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:127729056A>G	uc003kuu.3	-	9	1676	c.1237T>C	c.(1237-1239)Tat>Cat	p.Y413H	FBN2_uc003kuv.2_Missense_Mutation_p.Y380H	NM_001999	NP_001990	P35556	FBN2_HUMAN	Homo sapiens fibrillin 2 (FBN2), mRNA.	413	TB 2.				bone trabecula formation|negative regulation of transforming growth factor beta receptor signaling pathway by extracellular sequestering of TGFbeta|positive regulation of bone mineralization|positive regulation of osteoblast differentiation	microfibril	calcium ion binding|extracellular matrix structural constituent			NS(1)|autonomic_ganglia(1)|biliary_tract(1)|breast(1)|endometrium(15)|haematopoietic_and_lymphoid_tissue(4)|kidney(13)|large_intestine(37)|liver(1)|lung(89)|ovary(9)|pancreas(2)|prostate(6)|skin(10)|stomach(1)|upper_aerodigestive_tract(5)|urinary_tract(1)	197		all_cancers(142;0.0216)|Prostate(80;0.0551)	KIRC - Kidney renal clear cell carcinoma(527;0.0268)|Kidney(363;0.0488)	OV - Ovarian serous cystadenocarcinoma(64;0.0821)|Epithelial(69;0.146)		AGTCTGCGATATTCCTCTAGA	0.473												
SPOCK1	6695	broad.mit.edu	37	5	136314406	136314406	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:136314406G>A	uc003lbo.3	-	9	1448	c.1257C>T	c.(1255-1257)gcC>gcT	p.A419A	SPOCK1_uc003lbp.3_Silent_p.A419A	NM_004598	NP_004589	Q08629	TICN1_HUMAN	Homo sapiens sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 (SPOCK1), mRNA.	419					cell adhesion|cell proliferation|cellular component movement|nervous system development|signal transduction	proteinaceous extracellular matrix	calcium ion binding			breast(1)|endometrium(3)|kidney(1)|large_intestine(4)|liver(2)|lung(4)|ovary(1)|pancreas(1)|stomach(1)	18			KIRC - Kidney renal clear cell carcinoma(527;0.0101)|Kidney(363;0.0233)			CCTCTGTCACGGCTCGGGTGT	0.522												
PCDHAC2	56146	broad.mit.edu	37	5	140174848	140174848	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:140174848C>T	uc003lhd.2	+	0	405	c.299C>T	c.(298-300)gCg>gTg	p.A100V	PCDHAC2_uc003lha.2_Intron|PCDHAC2_uc003lhb.2_Intron|PCDHAC2_uc003lhc.1_Missense_Mutation_p.A100V|PCDHAC2_uc011czy.2_Missense_Mutation_p.A100V	NM_018905	NP_061728	Q9Y5I4	PCDC2_HUMAN	Homo sapiens protocadherin alpha 2 (PCDHA2), transcript variant 1, mRNA.	115	Cadherin 1.				homophilic cell adhesion|nervous system development	integral to plasma membrane	calcium ion binding			NS(1)|breast(1)|endometrium(4)|kidney(4)|large_intestine(10)|liver(2)|lung(9)|ovary(2)|prostate(1)|skin(7)|upper_aerodigestive_tract(3)|urinary_tract(1)	45			KIRC - Kidney renal clear cell carcinoma(527;0.00112)|Kidney(363;0.00191)			GGGCGGAGCGCGGAATGTAGC	0.542												
PCDHB6	56130	broad.mit.edu	37	5	140531524	140531524	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:140531524G>A	uc003lir.3	+	0	1686	c.1686G>A	c.(1684-1686)ccG>ccA	p.P562P		NM_018939	NP_061762	Q9Y5E3	PCDB6_HUMAN	Homo sapiens protocadherin beta 6 (PCDHB6), mRNA.	562					calcium-dependent cell-cell adhesion|homophilic cell adhesion|synapse assembly|synaptic transmission	integral to plasma membrane	calcium ion binding			cervix(1)|endometrium(14)|kidney(6)|large_intestine(16)|liver(1)|lung(33)|ovary(1)|pancreas(2)|prostate(1)|skin(6)|upper_aerodigestive_tract(2)|urinary_tract(1)	84			KIRC - Kidney renal clear cell carcinoma(527;0.00185)|Kidney(363;0.00339)			TGTTGTACCCGCTGCAGAACG	0.726												
UNC5A	90249	broad.mit.edu	37	5	176301280	176301280	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:176301280T>C	uc003mey.3	+	7	1283	c.1091T>C	c.(1090-1092)cTc>cCc	p.L364P	UNC5A_uc010jkg.1_Missense_Mutation_p.L324P	NM_133369	NP_588610	Q6ZN44	UNC5A_HUMAN	Homo sapiens unc-5 homolog A (C. elegans) (UNC5A), mRNA.	364					apoptosis|axon guidance|regulation of apoptosis	integral to membrane|plasma membrane				endometrium(4)|kidney(3)|large_intestine(2)|lung(14)|ovary(1)|pancreas(1)|prostate(1)|skin(6)|upper_aerodigestive_tract(2)	34	all_cancers(89;0.000119)|Renal(175;0.000269)|Lung NSC(126;0.00696)|all_lung(126;0.0115)	Medulloblastoma(196;0.00498)|all_neural(177;0.0138)	Kidney(164;2.23e-05)|KIRC - Kidney renal clear cell carcinoma(164;0.000178)			CCCCATCTGCTCACCATCCAG	0.642												
GMCL1P1	64396	broad.mit.edu	37	5	177612751	177612751	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr5:177612751T>C	uc003mit.1	-	0	1683	c.1550A>G	c.(1549-1551)aAt>aGt	p.N517S						Homo sapiens germ cell-less homolog 1 (Drosophila) pseudogene 1 (GMCL1P1), non-coding RNA.																		GTGACGATTATTTTCAATTCC	0.383												
DPCR1	135656	broad.mit.edu	37	6	30919701	30919701	+	Silent	SNP	T	T	C	rs114468580	byFrequency	TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr6:30919701T>C	uc003nsg.2	+	1	3460	c.3460T>C	c.(3460-3462)Ttg>Ctg	p.L1154L		NM_080870	NP_543146	Q3MIW9	DPCR1_HUMAN	Homo sapiens diffuse panbronchiolitis critical region 1 (DPCR1), mRNA.	293						integral to membrane				endometrium(1)|kidney(2)|large_intestine(3)|lung(3)|pancreas(1)	10						AAGGACCACATTGGCCCATGA	0.473												
SKIV2L	6499	broad.mit.edu	37	6	31936254	31936254	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr6:31936254G>A	uc003nyn.1	+	23	3397	c.3008G>A	c.(3007-3009)cGg>cAg	p.R1003Q	SKIV2L_uc011dou.1_Missense_Mutation_p.R845Q|SKIV2L_uc011dov.1_Missense_Mutation_p.R810Q|STK19_uc003nyt.3_5'Flank	NM_006929	NP_008860	Q15477	SKIV2_HUMAN	Homo sapiens superkiller viralicidic activity 2-like (S. cerevisiae) (SKIV2L), mRNA.	1003						nucleus	ATP binding|ATP-dependent RNA helicase activity|protein binding|RNA binding			breast(1)|central_nervous_system(1)|large_intestine(1)|ovary(1)	4						CTCCGGGCCCGGAAGCTGGAG	0.632												
DNAH8	1769	broad.mit.edu	37	6	38903432	38903432	+	Missense_Mutation	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr6:38903432A>G	uc021yzh.1	+	76	11631	c.11522A>G	c.(11521-11523)gAa>gGa	p.E3841G	DNAH8_uc003ooe.2_Missense_Mutation_p.E3624G|DNAH8_uc003oog.1_Missense_Mutation_p.E73G|LOC100131047_uc003oof.2_Intron	NM_001206927	NP_001193856			Homo sapiens dynein, axonemal, heavy chain 8 (DNAH8), mRNA.											NS(7)|breast(9)|central_nervous_system(4)|cervix(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(3)|kidney(16)|large_intestine(44)|liver(4)|lung(101)|ovary(7)|pancreas(2)|prostate(8)|skin(28)|stomach(4)|upper_aerodigestive_tract(6)|urinary_tract(4)	260						AAGATGAAAGAACTTGAAGAT	0.308												
PKHD1	5314	broad.mit.edu	37	6	51497434	51497434	+	Missense_Mutation	SNP	A	A	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr6:51497434A>T	uc003pah.1	-	64	11870	c.11594T>A	c.(11593-11595)cTg>cAg	p.L3865Q		NM_138694	NP_619639	P08F94	PKHD1_HUMAN	Homo sapiens polycystic kidney and hepatic disease 1 (autosomal recessive) (PKHD1), transcript variant 1, mRNA.	3865					cell-cell adhesion|cilium assembly|homeostatic process|kidney development|negative regulation of cellular component movement	anchored to external side of plasma membrane|apical plasma membrane|integral to membrane|microtubule basal body	protein binding|receptor activity			NS(1)|autonomic_ganglia(1)|breast(8)|central_nervous_system(5)|cervix(1)|endometrium(16)|haematopoietic_and_lymphoid_tissue(4)|kidney(11)|large_intestine(59)|lung(139)|ovary(16)|prostate(8)|skin(20)|soft_tissue(1)|stomach(2)|upper_aerodigestive_tract(7)|urinary_tract(5)	304	Lung NSC(77;0.0605)					CACAGAGGACAGGGAAGCAGC	0.478												
DLL1	28514	broad.mit.edu	37	6	170592139	170592140	+	Frame_Shift_Ins	INS	-	-	TC			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr6:170592139_170592140insTC	uc003qxm.3	-	9	2572_2573	c.2102_2103insGA	c.(2101-2103)gacfs	p.D701fs		NM_005618	NP_005609	O00548	DLL1_HUMAN	Homo sapiens delta-like 1 (Drosophila) (DLL1), mRNA.	701					cell communication|cell fate determination|hemopoiesis|Notch receptor processing|Notch signaling pathway|regulation of cell adhesion	extracellular region|integral to plasma membrane	calcium ion binding|Notch binding			NS(2)|breast(1)|endometrium(1)|large_intestine(7)|lung(17)|ovary(1)|prostate(2)|skin(1)|urinary_tract(1)	33		Breast(66;5.08e-05)|Ovarian(120;0.125)|Esophageal squamous(34;0.246)		OV - Ovarian serous cystadenocarcinoma(33;6.71e-23)|BRCA - Breast invasive adenocarcinoma(81;4.81e-06)|GBM - Glioblastoma multiforme(31;0.0584)		GGTACTTGGTGTCTTTTGAAGT	0.485												
ZNF679	168417	broad.mit.edu	37	7	63709526	63709526	+	Silent	SNP	C	C	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:63709526C>A	uc003tsx.3	+	1	300	c.31C>A	c.(31-33)Cga>Aga	p.R11R		NM_153363	NP_699194	Q8IYX0	ZN679_HUMAN	Homo sapiens zinc finger protein 679 (ZNF679), mRNA.	11					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			endometrium(2)|kidney(3)|lung(11)|skin(1)|stomach(1)	18						CCCTGGAAGCCGAGAAATGGT	0.572												
GATS	352954	broad.mit.edu	37	7	99821643	99821643	+	Silent	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:99821643G>A	uc003uua.4	-	2	522	c.273C>T	c.(271-273)aaC>aaT	p.N91N	GATS_uc010lgt.3_Non-coding_Transcript|GATS_uc003uty.4_Non-coding_Transcript|GATS_uc003utz.4_Non-coding_Transcript|GATS_uc011kjl.2_5'Flank|GATS_uc010lgu.2_Non-coding_Transcript	NM_178831	NP_849153	Q8NAP1	GATS_HUMAN	Homo sapiens GATS, stromal antigen 3 opposite strand (GATS), transcript variant 1, mRNA.	91										endometrium(2)|large_intestine(2)|lung(4)	8	Lung NSC(181;0.0181)|all_lung(186;0.0284)|Esophageal squamous(72;0.0439)					CGGACACCACGTTCAGGGCCA	0.622												
C7orf53	286006	broad.mit.edu	37	7	112129963	112129963	+	Nonsense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:112129963C>T	uc011kmq.2	+	3	490	c.355C>T	c.(355-357)Cga>Tga	p.R119*	C7orf53_uc003vgl.3_Non-coding_Transcript|C7orf53_uc003vgm.3_Nonsense_Mutation_p.R119*	NM_001134468	NP_872403	Q8N8F7	CG053_HUMAN	Homo sapiens chromosome 7 open reading frame 53 (C7orf53), transcript variant 2, mRNA.	119						integral to membrane				endometrium(1)|large_intestine(2)|ovary(1)	4						GATCGTAAAGCGACTCAACCA	0.388												
PLXNA4	91584	broad.mit.edu	37	7	131817922	131817922	+	Silent	SNP	G	G	A	rs114567124	by1000genomes	TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:131817922G>A	uc003vra.4	-	30	5704	c.5475C>T	c.(5473-5475)agC>agT	p.S1825S	PLXNA4_uc003vqz.4_Silent_p.S110S	NM_020911	NP_065962	Q9HCM2	PLXA4_HUMAN	Homo sapiens plexin A4 (PLXNA4), transcript variant 1, mRNA.	1825						integral to membrane|intracellular|plasma membrane				NS(1)|breast(1)|endometrium(3)|kidney(4)|large_intestine(14)|lung(17)|ovary(1)|prostate(2)|skin(1)|stomach(1)	45						TGTCTTGGTCGCTGATGGCTG	0.507												
SVOPL	136306	broad.mit.edu	37	7	138305867	138305867	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:138305867G>A	uc011kqh.2	-	12	1277	c.1277C>T	c.(1276-1278)aCg>aTg	p.T426M	SVOPL_uc003vue.3_Missense_Mutation_p.T274M	NM_001139456	NP_001132928	Q8N434	SVOPL_HUMAN	Homo sapiens SVOP-like (SVOPL), transcript variant 1, mRNA.	426						integral to membrane	transmembrane transporter activity			NS(1)|endometrium(2)|kidney(1)|large_intestine(5)|lung(4)|ovary(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(3)	19						AGCGCGCATCGTGGTGGGGTA	0.597												
BRAF	673	broad.mit.edu	37	7	140453136	140453136	+	Missense_Mutation	SNP	A	A	T	rs121913377		TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:140453136A>T	uc003vwc.4	-	14	1860	c.1799T>A	c.(1798-1800)gTg>gAg	p.V600E		NM_004333	NP_004324	P15056	BRAF_HUMAN	Homo sapiens v-raf murine sarcoma viral oncogene homolog B1 (BRAF), mRNA.	600	Protein kinase.		V -> D (in a melanoma cell line; requires 2 nucleotide substitutions).|V -> E (in sarcoma, colorectal adenocarcinoma, metastatic melanoma, ovarian serous carcinoma, pilocytic astrocytoma; somatic mutation; most common mutation; constitutive and elevated kinase activity; efficiently induces cell transformation; suppression of mutation in melanoma causes growth arrest and promotes apoptosis).		activation of MAPKK activity|anti-apoptosis|nerve growth factor receptor signaling pathway|organ morphogenesis|positive regulation of peptidyl-serine phosphorylation|small GTPase mediated signal transduction|synaptic transmission	cytosol|nucleus|plasma membrane	ATP binding|metal ion binding	p.V600E(41204)|p.V600K(615)|p.V600?(377)|p.V600R(99)|p.V600D(40)|p.V600_K601>E(30)|p.V600L(28)|p.V600A(24)|p.V600G(22)|p.V600M(22)|p.A598_T599insV(7)|p.T599_V600insT(7)|p.T599I(5)|p.V600Q(4)|p.T599_R603>I(4)|p.T599_V600insTT(3)|p.T599_V600insDFGLAT(2)|p.T599_V600>IAL(2)|p.V600_S605>EK(2)|p.T599T(2)|p.V600_S605>DV(2)|p.V600_S605>D(2)|p.V600_W604del(1)|p.V600V(1)|p.T599_V600insV(1)|p.V600>DLAT(1)|p.D594_T599del(1)	SLC45A3/BRAF(2)|AGTRAP/BRAF(2)|FAM131B_ENST00000443739/BRAF(7)|AKAP9_ENST00000356239/BRAF(10)|KIAA1549/BRAF(703)|FCHSD1/BRAF(2)	NS(588)|adrenal_gland(3)|autonomic_ganglia(3)|biliary_tract(29)|bone(7)|breast(21)|central_nervous_system(99)|cervix(6)|endometrium(33)|eye(72)|gastrointestinal_tract_(site_indeterminate)(2)|genital_tract(4)|haematopoietic_and_lymphoid_tissue(436)|kidney(3)|large_intestine(6953)|liver(17)|lung(192)|oesophagus(4)|ovary(275)|pancreas(15)|pituitary(1)|prostate(25)|salivary_gland(1)|skin(6285)|small_intestine(12)|soft_tissue(40)|stomach(11)|testis(7)|thyroid(12220)|upper_aerodigestive_tract(13)|urinary_tract(3)	27380	Melanoma(164;0.00956)				Sorafenib(DB00398)	TCGAGATTTCACTGTAGCTAG	0.368	V600D(K029AX_SKIN)|V600D(WM115_SKIN)|V600D(WM2664_SKIN)|V600E(8505C_THYROID)|V600E(A101D_SKIN)|V600E(A2058_SKIN)|V600E(A375_SKIN)|V600E(A673_BONE)|V600E(AM38_CENTRAL_NERVOUS_SYSTEM)|V600E(BCPAP_THYROID)|V600E(BHT101_THYROID)|V600E(BT474_BREAST)|V600E(C32_SKIN)|V600E(CL34_LARGE_INTESTINE)|V600E(COLO205_LARGE_INTESTINE)|V600E(COLO679_SKIN)|V600E(COLO741_SKIN)|V600E(COLO783_SKIN)|V600E(COLO800_SKIN)|V600E(COLO818_SKIN)|V600E(COLO829_SKIN)|V600E(COLO849_SKIN)|V600E(DBTRG05MG_CENTRAL_NERVOUS_SYSTEM)|V600E(DU4475_BREAST)|V600E(ES2_OVARY)|V600E(G361_SKIN)|V600E(GCT_SOFT_TISSUE)|V600E(HS294T_SKIN)|V600E(HS695T_SKIN)|V600E(HS939T_SKIN)|V600E(IGR1_SKIN)|V600E(IGR37_SKIN)|V600E(IGR39_SKIN)|V600E(K029AX_SKIN)|V600E(KG1C_CENTRAL_NERVOUS_SYSTEM)|V600E(LOXIMVI_SKIN)|V600E(MALME3M_SKIN)|V600E(MELHO_SKIN)|V600E(OUMS23_LARGE_INTESTINE)|V600E(RKO_LARGE_INTESTINE)|V600E(RPMI7951_SKIN)|V600E(RVH421_SKIN)|V600E(SH4_SKIN)|V600E(SIGM5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|V600E(SKHEP1_LIVER)|V600E(SKMEL24_SKIN)|V600E(SKMEL28_SKIN)|V600E(SKMEL5_SKIN)|V600E(SW1417_LARGE_INTESTINE)|V600E(UACC257_SKIN)|V600E(UACC62_SKIN)|V600E(WM793_SKIN)|V600E(WM88_SKIN)|V600E(WM983B_SKIN)	61	"""Mis, T, O"""	"""AKAP9, KIAA1549"""	"""melanoma, colorectal, papillary thyroid, borderline ov, Non small-cell lung cancer (NSCLC), cholangiocarcinoma, pilocytic astrocytoma"""		Cardio-facio-cutaneous syndrome		Cardiofaciocutaneous syndrome			
C7orf33	202865	broad.mit.edu	37	7	148288176	148288176	+	Silent	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr7:148288176C>T	uc003wew.3	+	0	520	c.159C>T	c.(157-159)ggC>ggT	p.G53G		NM_145304	NP_660347	Q8WU49	CG033_HUMAN	Homo sapiens chromosome 7 open reading frame 33 (C7orf33), mRNA.	53								p.G53G(2)|p.G53C(1)		central_nervous_system(1)|large_intestine(4)|lung(7)|prostate(2)	14	Melanoma(164;0.15)		OV - Ovarian serous cystadenocarcinoma(82;0.00291)			ACGTTAGGGGCGGTCCAGGTC	0.512												
NPBWR1	2831	broad.mit.edu	37	8	53853296	53853296	+	Missense_Mutation	SNP	A	A	G			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr8:53853296A>G	uc011ldu.2	+	0	829	c.829A>G	c.(829-831)Acc>Gcc	p.T277A		NM_005285	NP_005276	P48145	NPBW1_HUMAN	Homo sapiens neuropeptides B/W receptor 1 (NPBWR1), mRNA.	277					synaptic transmission	plasma membrane	opioid receptor activity|protein binding			breast(1)|endometrium(2)|kidney(1)|large_intestine(3)|lung(8)|ovary(2)	17		Lung NSC(129;0.0222)|all_epithelial(80;0.0301)|all_lung(136;0.0431)				GGCGCTCACCACCGACCTCCC	0.642												
KCNS2	3788	broad.mit.edu	37	8	99441064	99441064	+	Missense_Mutation	SNP	C	C	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr8:99441064C>A	uc003yin.3	+	1	1207	c.857C>A	c.(856-858)aCt>aAt	p.T286N	KCNS2_uc022azb.1_Missense_Mutation_p.T286N	NM_020697	NP_065748	Q9ULS6	KCNS2_HUMAN	Homo sapiens potassium voltage-gated channel, delayed-rectifier, subfamily S, member 2 (KCNS2), mRNA.	286						voltage-gated potassium channel complex	voltage-gated potassium channel activity			autonomic_ganglia(1)|breast(2)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(6)|lung(11)|ovary(1)|prostate(1)|skin(1)|urinary_tract(2)	31	Breast(36;2.4e-06)		OV - Ovarian serous cystadenocarcinoma(57;0.0448)			AGCACACCTACTTTAGCCAAC	0.557												
JAK2	3717	broad.mit.edu	37	9	5073770	5073770	+	Missense_Mutation	SNP	G	G	T	rs77375493		TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr9:5073770G>T	uc010mhm.3	+	12	1962	c.1849G>T	c.(1849-1851)Gtc>Ttc	p.V617F	JAK2_uc003ziw.3_Missense_Mutation_p.V617F	NM_004972	NP_004963	O60674	JAK2_HUMAN	Homo sapiens Janus kinase 2 (JAK2), mRNA.	617	Protein kinase 1.		V -> F (in PV and AML; associated with susceptibility to Budd-Chiari syndrome; somatic mutation in a high percentage of patients with essential thrombocythemia or myelofibrosis; leads to constitutive tyrosine phosphorylation activity that promotes cytokine hypersensitivity).		actin filament polymerization|activation of caspase activity by protein phosphorylation|activation of JAK2 kinase activity|blood coagulation|cellular component movement|erythrocyte differentiation|interferon-gamma-mediated signaling pathway|interleukin-12-mediated signaling pathway|JAK-STAT cascade involved in growth hormone signaling pathway|mammary gland epithelium development|mesoderm development|negative regulation of cell proliferation|negative regulation of DNA binding|positive regulation of apoptosis|positive regulation of cell-substrate adhesion|positive regulation of growth hormone receptor signaling pathway|positive regulation of nitric-oxide synthase 2 biosynthetic process|positive regulation of phosphatidylinositol 3-kinase cascade|positive regulation of tumor necrosis factor production|positive regulation of tyrosine phosphorylation of Stat3 protein|positive regulation of tyrosine phosphorylation of Stat5 protein|protein autophosphorylation|regulation of inflammatory response|regulation of interferon-gamma-mediated signaling pathway|response to antibiotic|response to lipopolysaccharide|STAT protein import into nucleus|tumor necrosis factor-mediated signaling pathway|tyrosine phosphorylation of STAT protein	caveola|cytoskeleton|cytosol|endomembrane system|nucleus	ATP binding|growth hormone receptor binding|heme binding|histone binding|histone kinase activity (H3-Y41 specific)|interleukin-12 receptor binding|non-membrane spanning protein tyrosine kinase activity|protein kinase binding|SH2 domain binding	p.V617F(62453)|p.V617_C618>FR(4)|p.V617I(2)|p.C616Y(1)|p.V617V(1)	BCR/JAK2(6)|SSBP2/JAK2(4)|SEC31A/JAK2(4)|ETV6/JAK2(11)|PCM1/JAK2(30)|PAX5/JAK2(18)	breast(5)|endometrium(4)|haematopoietic_and_lymphoid_tissue(32944)|kidney(4)|large_intestine(10)|liver(1)|lung(20)|ovary(3)|prostate(4)|skin(2)|urinary_tract(1)	32998	all_hematologic(13;0.137)	Acute lymphoblastic leukemia(23;0.0198)|Breast(48;0.147)		GBM - Glioblastoma multiforme(50;0.0237)|Lung(218;0.133)		TGGAGTATGTGTCTGTGGAGA	0.343	V617F(HEL9217_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)	1	"""T, Mis, O"""	"""ETV6, PCM1, BCR"""	"""ALL, AML, MPD,  CML"""				Polycythemia Vera, Familial			
FBP1	2203	broad.mit.edu	37	9	97367792	97367792	+	Missense_Mutation	SNP	C	C	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr9:97367792C>A	uc004auw.4	-	5	1103	c.772G>T	c.(772-774)Gtc>Ttc	p.V258F	FBP1_uc010mrl.3_Missense_Mutation_p.V258F	NM_000507	NP_001121100	P09467	F16P1_HUMAN	Homo sapiens fructose-1,6-bisphosphatase 1 (FBP1), transcript variant 1, mRNA.	258					gluconeogenesis	cytosol	fructose 1,6-bisphosphate 1-phosphatase activity|fructose-2,6-bisphosphate 2-phosphatase activity|identical protein binding|metal ion binding			kidney(1)|liver(1)|lung(1)	3		Acute lymphoblastic leukemia(62;0.136)			Adenosine monophosphate(DB00131)	CCTCCGTAGACCAGAGTGCGA	0.512												
LHX2	9355	broad.mit.edu	37	9	126794913	126794913	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr9:126794913C>T	uc010mwi.1	+	4	1911	c.1172C>T	c.(1171-1173)aCt>aTt	p.T391I	LHX2_uc004boe.1_Missense_Mutation_p.T383I	NM_004789	NP_004780	P50458	LHX2_HUMAN	Homo sapiens LIM homeobox 2 (LHX2), mRNA.	383				GHEPHSPSQTTLTNLF -> AMSLTAPHKRLLPTFSNDSQP PHPTISLKKKLSLV (in Ref. 1; AAB08752).		nucleus	sequence-specific DNA binding transcription factor activity|zinc ion binding			endometrium(1)|kidney(2)|large_intestine(2)|lung(4)|prostate(1)	10						TCCGTCTTAACTTCTGTGCCT	0.592												
PNPLA7	375775	broad.mit.edu	37	9	140374853	140374853	+	Missense_Mutation	SNP	T	T	C			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chr9:140374853T>C	uc010ncj.1	-	22	2828	c.2491A>G	c.(2491-2493)Acg>Gcg	p.T831A	PNPLA7_uc004cnd.1_Missense_Mutation_p.T72A|PNPLA7_uc004cne.1_Missense_Mutation_p.T72A|PNPLA7_uc011mfa.1_Missense_Mutation_p.T214A|PNPLA7_uc004cnf.2_Missense_Mutation_p.T806A	NM_001098537	NP_001092007	Q6ZV29	PLPL7_HUMAN	Homo sapiens patatin-like phospholipase domain containing 7 (PNPLA7), transcript variant 1, mRNA.	806					lipid metabolic process	endoplasmic reticulum|integral to membrane|lysosomal membrane|microsome|mitochondrial membrane|nuclear membrane	hydrolase activity			breast(1)|central_nervous_system(3)|endometrium(2)|haematopoietic_and_lymphoid_tissue(3)|large_intestine(9)|lung(13)|ovary(1)|prostate(1)|skin(2)|stomach(3)|upper_aerodigestive_tract(1)|urinary_tract(1)	40	all_cancers(76;0.126)			OV - Ovarian serous cystadenocarcinoma(145;0.000268)|Epithelial(140;0.000839)		GGTGTGAGCGTGCCATCTACC	0.662												
ARSF	416	broad.mit.edu	37	X	3021841	3021841	+	Missense_Mutation	SNP	G	G	A			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chrX:3021841G>A	uc022brz.1	+	8	1277	c.1141G>A	c.(1141-1143)Gtc>Atc	p.V381I	ARSF_uc004cre.2_Missense_Mutation_p.V381I|ARSF_uc004crf.2_Missense_Mutation_p.V381I	NM_001201538	NP_001188467	P54793	ARSF_HUMAN	Homo sapiens arylsulfatase F (ARSF), transcript variant 2, mRNA.	381						extracellular region	arylsulfatase activity|metal ion binding	p.V381I(2)		NS(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(8)|lung(15)|ovary(2)|prostate(3)|skin(3)|urinary_tract(2)	38		all_cancers(21;4.28e-07)|all_epithelial(21;2.07e-08)|all_lung(23;2.81e-05)|Lung NSC(23;0.000693)|Lung SC(21;0.122)				TGGAATCCGCGTCCCAGGAAT	0.438												
BRWD3	254065	broad.mit.edu	37	X	79999713	79999713	+	Missense_Mutation	SNP	C	C	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chrX:79999713C>T	uc004edt.3	-	7	894	c.631G>A	c.(631-633)Gat>Aat	p.D211N	BRWD3_uc004edp.3_Missense_Mutation_p.D40N|BRWD3_uc004edq.3_5'UTR|BRWD3_uc010nmj.2_5'UTR|BRWD3_uc004edr.3_5'UTR|BRWD3_uc004eds.3_5'UTR|BRWD3_uc004edo.3_5'UTR|BRWD3_uc004edu.3_5'UTR|BRWD3_uc004edv.3_5'UTR|BRWD3_uc004edw.3_5'UTR|BRWD3_uc004edx.3_5'UTR|BRWD3_uc004edy.3_5'UTR|BRWD3_uc004edz.3_5'UTR|BRWD3_uc004eea.3_5'UTR|BRWD3_uc004eeb.3_Intron	NM_153252	NP_694984	Q6RI45	BRWD3_HUMAN	Homo sapiens bromodomain and WD repeat domain containing 3 (BRWD3), mRNA.	211										breast(4)|cervix(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(18)|lung(39)|ovary(4)|prostate(2)|skin(3)	87						AGGCGTCCATCATCTGTAGCC	0.403												
FATE1	89885	broad.mit.edu	37	X	150885868	150885868	+	Missense_Mutation	SNP	A	A	T			TCGA-76-4928-01B-01D-1486-08	TCGA-76-4928-10A-01D-1486-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	6e30f277-875e-4ab8-bc7c-0a5121cde6d1	245a59f0-a6c4-4e1a-bd0a-d104308b123c	g.chrX:150885868A>T	uc004fex.3	+	1	315	c.231A>T	c.(229-231)aaA>aaT	p.K77N		NM_033085	NP_149076	Q969F0	FATE1_HUMAN	Homo sapiens fetal and adult testis expressed 1 (FATE1), mRNA.	77						endoplasmic reticulum|integral to membrane				NS(1)|breast(1)|cervix(1)|endometrium(3)|large_intestine(2)|lung(6)|ovary(1)	15	Acute lymphoblastic leukemia(192;6.56e-05)					GACCCAAGAAAATGGTACTGT	0.562												
