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
RNF207	388591	broad.mit.edu	37	1	6271141	6271141	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:6271141C>T	uc001amg.3	+	11	1246	c.1072C>T	c.(1072-1074)Cca>Tca	p.P358S	RNF207_uc010nzp.1_Non-coding_Transcript	NM_207396	NP_997279	Q6ZRF8	RN207_HUMAN	Homo sapiens ring finger protein 207 (RNF207), mRNA.	358						intracellular	zinc ion binding			endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(4)|lung(7)|ovary(2)	16	Ovarian(185;0.0634)	all_cancers(23;1.22e-38)|all_epithelial(116;4.25e-22)|all_lung(118;7.95e-08)|Lung NSC(185;1.6e-06)|all_neural(13;3.18e-06)|all_hematologic(16;8.99e-06)|Acute lymphoblastic leukemia(12;0.000365)|Breast(487;0.000496)|Renal(390;0.0007)|Colorectal(325;0.00104)|Glioma(11;0.00203)|Hepatocellular(190;0.00308)|Myeloproliferative disorder(586;0.0255)|Ovarian(437;0.0392)|Medulloblastoma(700;0.211)		Epithelial(90;4.84e-38)|GBM - Glioblastoma multiforme(13;5.77e-32)|OV - Ovarian serous cystadenocarcinoma(86;2.88e-19)|Colorectal(212;6.9e-08)|COAD - Colon adenocarcinoma(227;8.13e-06)|Kidney(185;4.89e-05)|KIRC - Kidney renal clear cell carcinoma(229;0.000896)|BRCA - Breast invasive adenocarcinoma(365;0.00108)|STAD - Stomach adenocarcinoma(132;0.00311)|READ - Rectum adenocarcinoma(331;0.0642)|Lung(427;0.182)		GCTGCTGGGGCCACGTCGGGT	0.667												
CAMTA1	23261	broad.mit.edu	37	1	7723936	7723936	+	Silent	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:7723936C>T	uc001aoi.3	+	8	1536	c.1329C>T	c.(1327-1329)gcC>gcT	p.A443A		NM_015215	NP_056030	Q9Y6Y1	CMTA1_HUMAN	Homo sapiens calmodulin binding transcription activator 1 (CAMTA1), transcript variant 1, mRNA.	443					regulation of transcription, DNA-dependent|transcription, DNA-dependent	cytoplasm|nucleus	calmodulin binding			breast(5)|central_nervous_system(4)|cervix(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(3)|kidney(3)|large_intestine(11)|lung(29)|ovary(5)|pancreas(2)|prostate(4)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(3)	85	Ovarian(185;0.0634)	all_epithelial(116;8.38e-23)|all_lung(118;5.87e-07)|Lung NSC(185;3.43e-06)|Renal(390;0.000219)|Breast(487;0.000307)|Colorectal(325;0.000615)|Hepatocellular(190;0.0088)|Myeloproliferative disorder(586;0.0303)|Ovarian(437;0.0388)		UCEC - Uterine corpus endometrioid carcinoma (279;0.101)|Colorectal(212;1.33e-05)|COAD - Colon adenocarcinoma(227;0.000235)|BRCA - Breast invasive adenocarcinoma(304;0.000864)|Kidney(185;0.00244)|STAD - Stomach adenocarcinoma(132;0.00644)|KIRC - Kidney renal clear cell carcinoma(229;0.0179)|READ - Rectum adenocarcinoma(331;0.133)		ACAAGTTCGCCTTTCCCACCA	0.652			T	WWTR1	epitheliod hemangioendothelioma							
CAMTA1	23261	broad.mit.edu	37	1	7723997	7723997	+	Silent	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:7723997C>T	uc001aoi.3	+	8	1597	c.1390C>T	c.(1390-1392)Ctg>Ttg	p.L464L		NM_015215	NP_056030	Q9Y6Y1	CMTA1_HUMAN	Homo sapiens calmodulin binding transcription activator 1 (CAMTA1), transcript variant 1, mRNA.	464					regulation of transcription, DNA-dependent|transcription, DNA-dependent	cytoplasm|nucleus	calmodulin binding			breast(5)|central_nervous_system(4)|cervix(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(3)|kidney(3)|large_intestine(11)|lung(29)|ovary(5)|pancreas(2)|prostate(4)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(3)	85	Ovarian(185;0.0634)	all_epithelial(116;8.38e-23)|all_lung(118;5.87e-07)|Lung NSC(185;3.43e-06)|Renal(390;0.000219)|Breast(487;0.000307)|Colorectal(325;0.000615)|Hepatocellular(190;0.0088)|Myeloproliferative disorder(586;0.0303)|Ovarian(437;0.0388)		UCEC - Uterine corpus endometrioid carcinoma (279;0.101)|Colorectal(212;1.33e-05)|COAD - Colon adenocarcinoma(227;0.000235)|BRCA - Breast invasive adenocarcinoma(304;0.000864)|Kidney(185;0.00244)|STAD - Stomach adenocarcinoma(132;0.00644)|KIRC - Kidney renal clear cell carcinoma(229;0.0179)|READ - Rectum adenocarcinoma(331;0.133)		GTCCGAAGAGCTGGTCCTCTC	0.597			T	WWTR1	epitheliod hemangioendothelioma							
FHL3	2275	broad.mit.edu	37	1	38463709	38463709	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:38463709G>A	uc001cck.3	-	3	606	c.427C>T	c.(427-429)Ccc>Tcc	p.P143S	FHL3_uc001ccm.3_Missense_Mutation_p.P35S|FHL3_uc009vvl.2_Missense_Mutation_p.P143S	NM_004468	NP_004459	Q13643	FHL3_HUMAN	Homo sapiens four and a half LIM domains 3 (FHL3), transcript variant 1, mRNA.	143	LIM zinc-binding 2.				muscle organ development		zinc ion binding	p.P143S(2)		endometrium(1)|kidney(1)|large_intestine(1)|lung(2)	5	Acute lymphoblastic leukemia(166;0.074)|all_hematologic(146;0.197)	Myeloproliferative disorder(586;0.0255)				CCCTTGTCGGGCACAAAAGAA	0.622												
PSMA5	5686	broad.mit.edu	37	1	109964523	109964523	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:109964523C>T	uc001dxn.3	-	1	173	c.55G>A	c.(55-57)Gga>Aga	p.G19R	PSMA5_uc010ovj.2_Intron|PSMA5_uc021ord.1_5'UTR|PSMA5_uc021ore.1_5'UTR	NM_002790	NP_001186703	P28066	PSA5_HUMAN	Homo sapiens proteasome (prosome, macropain) subunit, alpha type, 5 (PSMA5), transcript variant 1, mRNA.	19					anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process|apoptosis|DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest|G1/S transition of mitotic cell cycle|M/G1 transition of mitotic cell cycle|mRNA metabolic process|negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle|positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle|regulation of apoptosis|regulation of cellular amino acid metabolic process|S phase of mitotic cell cycle|viral reproduction	cytoplasm|nucleus|proteasome core complex, alpha-subunit complex	protein binding|threonine-type endopeptidase activity			kidney(1)|large_intestine(2)|lung(2)	5		all_epithelial(167;2.83e-05)|all_lung(203;0.00016)|Lung NSC(277;0.000318)|Breast(1374;0.244)		Lung(183;0.045)|Colorectal(144;0.116)|Epithelial(280;0.187)|all cancers(265;0.196)|LUSC - Lung squamous cell carcinoma(189;0.235)		AATAATCTTCCTTCGGGAGAA	0.348												
SPAG17	200162	broad.mit.edu	37	1	118640437	118640437	+	Missense_Mutation	SNP	T	T	C			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:118640437T>C	uc001ehk.2	-	6	935	c.867A>G	c.(865-867)atA>atG	p.I289M		NM_206996	NP_996879	Q6Q759	SPG17_HUMAN	Homo sapiens sperm associated antigen 17 (SPAG17), mRNA.	289						cilium|flagellar axoneme|microtubule				NS(1)|biliary_tract(1)|breast(2)|cervix(1)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(30)|liver(2)|lung(56)|ovary(3)|prostate(5)|skin(5)|upper_aerodigestive_tract(6)|urinary_tract(1)	123	Esophageal squamous(2;0.0106)	all_cancers(81;0.0204)|all_lung(203;9.46e-05)|Lung NSC(69;0.000675)|all_epithelial(167;0.01)		Lung(183;0.0858)		TAAGCTCTTTTATGGCATTTT	0.333												
NBPF10	100132406	broad.mit.edu	37	1	145325997	145325997	+	Silent	SNP	A	A	G			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:145325997A>G	uc021oul.1	+	29	3905	c.3870A>G	c.(3868-3870)caA>caG	p.Q1290Q	NBPF10_uc021ots.1_Intron|NBPF10_uc010oye.2_Intron|NBPF10_uc010oyi.2_Intron|NBPF10_uc010oyj.2_Intron|NBPF10_uc010oyl.2_Intron|NBPF10_uc001enc.2_Intron|NBPF10_uc021oum.1_Intron|NBPF10_uc021oun.1_Intron|NBPF10_uc021ouo.1_Intron|NBPF10_uc021oup.1_Intron|NBPF10_uc010oyp.1_Intron	NM_001039703	NP_001034792	A6NDV3	A6NDV3_HUMAN	Homo sapiens neuroblastoma breakpoint family, member 10 (NBPF10), mRNA.	1290										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)		AAGTCTTGCAAGACTCACTGG	0.468												
LOC728989	728989	broad.mit.edu	37	1	146494537	146494537	+	Silent	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:146494537C>T	uc001epd.2	-	3	536	c.462G>A	c.(460-462)gcG>gcA	p.A154A						Homo sapiens phosphodiesterase 4D interacting protein pseudogene (LOC728989), non-coding RNA.																		TTGGCAGGGCCGCTCTCCAGA	0.567												
FCRLA	84824	broad.mit.edu	37	1	161682911	161682911	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:161682911C>T	uc001gbe.3	+	5	1132	c.890C>T	c.(889-891)cCa>cTa	p.P297L	FCRLA_uc001gbg.3_Missense_Mutation_p.P151L|FCRLA_uc009wup.3_Missense_Mutation_p.P107L|FCRLA_uc009wuq.3_Missense_Mutation_p.P56L|FCRLA_uc001gbd.3_Missense_Mutation_p.P291L|FCRLA_uc001gbf.3_Missense_Mutation_p.P202L|FCRLA_uc009wuo.3_Missense_Mutation_p.P157L	NM_001184866	NP_001171795	Q7L513	FCRLA_HUMAN	Homo sapiens Fc receptor-like A (FCRLA), transcript variant 1, mRNA.	274	Pro-rich.				cell differentiation	cytoplasm|extracellular region				breast(1)|kidney(12)|large_intestine(4)|lung(13)|prostate(1)|skin(2)|stomach(1)	34	all_cancers(52;2.55e-15)|all_hematologic(112;0.0359)		BRCA - Breast invasive adenocarcinoma(70;0.00301)			ACATTGAATCCAGCTCCTCAG	0.582												
CACNA1S	779	broad.mit.edu	37	1	201012596	201012596	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr1:201012596C>T	uc001gvv.3	-	39	5088	c.4861G>A	c.(4861-4863)Gtc>Atc	p.V1621I		NM_000069	NP_000060	Q13698	CAC1S_HUMAN	Homo sapiens calcium channel, voltage-dependent, L type, alpha 1S subunit (CACNA1S), mRNA.	1621					axon guidance	I band|T-tubule|voltage-gated calcium channel complex	high voltage-gated calcium channel activity			NS(2)|breast(4)|central_nervous_system(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(13)|large_intestine(19)|lung(37)|ovary(6)|prostate(3)|skin(5)|upper_aerodigestive_tract(2)|urinary_tract(2)	102					Magnesium Sulfate(DB00653)|Verapamil(DB00661)	TTGGCCATGACGGGGGGCAGG	0.567											OREG0014067	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
ABCG4	64137	broad.mit.edu	37	11	119031668	119031668	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr11:119031668C>T	uc001pvs.3	+	14	2129	c.1793C>T	c.(1792-1794)cCg>cTg	p.P598L	ABCG4_uc009zar.3_Missense_Mutation_p.P598L	NM_022169	NP_071452	Q9H172	ABCG4_HUMAN	Homo sapiens ATP-binding cassette, sub-family G (WHITE), member 4 (ABCG4), transcript variant 1, mRNA.	598	ABC transmembrane type-2.				cholesterol efflux	integral to membrane	ATP binding|ATPase activity|protein heterodimerization activity|protein homodimerization activity			breast(1)|central_nervous_system(1)|endometrium(2)|kidney(2)|large_intestine(6)|lung(28)|ovary(2)|prostate(1)|skin(1)	44	all_hematologic(175;0.0977)	Medulloblastoma(222;0.0425)|Breast(348;0.052)|all_neural(223;0.112)		BRCA - Breast invasive adenocarcinoma(274;7.7e-05)		GAACGCTGCCCGTTCCGGGAG	0.567												
TSPAN9	10867	broad.mit.edu	37	12	3387673	3387673	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr12:3387673G>A	uc001qlp.3	+	3	333	c.150G>A	c.(148-150)tcG>tcA	p.S50S	TSPAN9_uc021qtd.1_Silent_p.S50S	NM_006675	NP_006666	O75954	TSN9_HUMAN	Homo sapiens tetraspanin 9 (TSPAN9), transcript variant 1, mRNA.	50						integral to plasma membrane|membrane fraction		p.P49H(1)		endometrium(1)|kidney(2)|large_intestine(3)|lung(1)|ovary(1)|prostate(2)|upper_aerodigestive_tract(1)	11			OV - Ovarian serous cystadenocarcinoma(31;0.00153)|COAD - Colon adenocarcinoma(12;0.0831)			GCTTCCCTTCGTTGTCTGCAG	0.597												
OR9K2	441639	broad.mit.edu	37	12	55524385	55524385	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr12:55524385G>A	uc010spe.2	+	0	833	c.833G>A	c.(832-834)gGt>gAt	p.G278D		NM_001005243	NP_001005243	Q8NGE7	OR9K2_HUMAN	Homo sapiens olfactory receptor, family 9, subfamily K, member 2 (OR9K2), mRNA.	278					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			NS(2)|breast(3)|central_nervous_system(1)|kidney(3)|large_intestine(3)|lung(14)|pancreas(1)|prostate(2)|skin(2)	31						GTGCTGTATGGTGCTGTCTTT	0.443												
APOF	319	broad.mit.edu	37	12	56755194	56755194	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr12:56755194C>T	uc001sle.1	-	1	850	c.796G>A	c.(796-798)Gca>Aca	p.A266T		NM_001638	NP_001629	Q13790	APOF_HUMAN	Homo sapiens apolipoprotein F (APOF), mRNA.	266					cholesterol metabolic process	high-density lipoprotein particle|low-density lipoprotein particle	cholesterol binding|lipid transporter activity|receptor binding			breast(1)|lung(3)|prostate(1)|stomach(1)	6						GAGATGTTTGCGTCTTTCTGA	0.493												
FOXN4	121643	broad.mit.edu	37	12	109719238	109719238	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr12:109719238G>A	uc001toe.4	-	8	1373	c.1268C>T	c.(1267-1269)cCg>cTg	p.P423L	FOXN4_uc009zvg.3_Missense_Mutation_p.P220L|FOXN4_uc001tof.4_Missense_Mutation_p.P243L	NM_213596	NP_998761	Q96NZ1	FOXN4_HUMAN	Homo sapiens forkhead box N4 (FOXN4), mRNA.	423					axon extension|embryo development|organ development|pattern specification process|regulation of heart contraction|regulation of sequence-specific DNA binding transcription factor activity|tissue development	transcription factor complex	DNA bending activity|double-stranded DNA binding|promoter binding|sequence-specific DNA binding|sequence-specific enhancer binding RNA polymerase II transcription factor activity|specific RNA polymerase II transcription factor activity|specific transcriptional repressor activity|transcription activator activity|transcription factor binding			large_intestine(5)|lung(9)|ovary(2)	16						CATGATGCTCGGGTCGAGGGC	0.627												
SERPINA12	145264	broad.mit.edu	37	14	94953819	94953819	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr14:94953819C>T	uc001ydj.3	-	5	1862	c.1066G>A	c.(1066-1068)Gct>Act	p.A356T		NM_173850	NP_776249	Q8IW75	SPA12_HUMAN	Homo sapiens serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 (SERPINA12), mRNA.	356					regulation of proteolysis	extracellular region	serine-type endopeptidase inhibitor activity			breast(1)|central_nervous_system(2)|endometrium(2)|kidney(3)|large_intestine(7)|lung(11)|ovary(1)|prostate(1)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1)	33				COAD - Colon adenocarcinoma(157;0.235)		TTCAGCTCAGCCTTGTGCACA	0.597												
PEPD	5184	broad.mit.edu	37	19	33892682	33892682	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr19:33892682G>A	uc002nur.4	-	11	1045	c.912C>T	c.(910-912)gcC>gcT	p.A304A	PEPD_uc010xrs.2_Silent_p.A240A|PEPD_uc010xrr.2_Silent_p.A263A	NM_000285	NP_000276	P12955	PEPD_HUMAN	Homo sapiens peptidase D (PEPD), transcript variant 1, mRNA.	304					cellular amino acid metabolic process|collagen catabolic process|proteolysis		aminopeptidase activity|dipeptidase activity|manganese ion binding|metallocarboxypeptidase activity			endometrium(3)|kidney(3)|large_intestine(2)|lung(7)|ovary(2)	17	Esophageal squamous(110;0.137)					CCTCATAGACGGCCTTCTGGT	0.627												
NLRP12	91662	broad.mit.edu	37	19	54313742	54313742	+	Missense_Mutation	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr19:54313742C>T	uc002qcj.4	-	2	1391	c.1171G>A	c.(1171-1173)Gtg>Atg	p.V391M	NLRP12_uc010eqw.3_5'Flank|NLRP12_uc002qch.4_Missense_Mutation_p.V391M|NLRP12_uc002qci.4_Missense_Mutation_p.V391M|NLRP12_uc002qck.4_Non-coding_Transcript|NLRP12_uc010eqx.3_Missense_Mutation_p.V391M	NM_144687	NP_653288	P59046	NAL12_HUMAN	Homo sapiens NLR family, pyrin domain containing 12 (NLRP12), transcript variant 2, mRNA.	391	NACHT.				negative regulation of I-kappaB kinase/NF-kappaB cascade|negative regulation of interleukin-1 secretion|negative regulation of interleukin-6 biosynthetic process|negative regulation of protein autophosphorylation|negative regulation of Toll signaling pathway|positive regulation of inflammatory response|positive regulation of interleukin-1 beta secretion|regulation of interleukin-18 biosynthetic process|release of cytoplasmic sequestered NF-kappaB	cytoplasm	ATP binding|caspase activator activity|protein binding			NS(1)|breast(4)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(17)|liver(1)|lung(36)|ovary(5)|pancreas(2)|skin(3)|upper_aerodigestive_tract(5)|urinary_tract(1)	80	Ovarian(34;0.19)			GBM - Glioblastoma multiforme(134;0.026)		TTGTCCCTCACGTAATTGAAG	0.562												
YIPF4	84272	broad.mit.edu	37	2	32530586	32530586	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:32530586G>A	uc002rok.3	+	5	893	c.626G>A	c.(625-627)aGt>aAt	p.S209N		NM_032312	NP_115688	Q9BSR8	YIPF4_HUMAN	Homo sapiens Yip1 domain family, member 4 (YIPF4), mRNA.	209						endoplasmic reticulum|integral to membrane	protein binding			kidney(2)|lung(3)|prostate(3)|skin(1)	9	Acute lymphoblastic leukemia(172;0.155)					GCTGCCTACAGTGCTGCTTCA	0.323												
RAB11FIP5	26056	broad.mit.edu	37	2	73315741	73315741	+	Silent	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:73315741C>T	uc002siu.4	-	2	1246	c.1005G>A	c.(1003-1005)tcG>tcA	p.S335S	RAB11FIP5_uc002sit.4_Silent_p.S257S	NM_015470	NP_056285	Q9BXF6	RFIP5_HUMAN	Homo sapiens RAB11 family interacting protein 5 (class I) (RAB11FIP5), mRNA.	335					protein transport	mitochondrial outer membrane|recycling endosome membrane	gamma-tubulin binding	p.S334F(1)		biliary_tract(1)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(3)|lung(9)|prostate(2)|skin(2)|upper_aerodigestive_tract(1)	23						TGACACAGAGCGAAGAGCGGG	0.622												
LCT	3938	broad.mit.edu	37	2	136566075	136566075	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:136566075G>A	uc002tuu.1	-	7	3853	c.3842C>T	c.(3841-3843)cCg>cTg	p.P1281L		NM_002299	NP_002290	P09848	LPH_HUMAN	Homo sapiens lactase (LCT), mRNA.	1281	4 X approximate repeats.				carbohydrate metabolic process|polysaccharide digestion	apical plasma membrane|integral to plasma membrane|membrane fraction	cation binding|glycosylceramidase activity|lactase activity			breast(6)|central_nervous_system(3)|cervix(1)|endometrium(8)|kidney(2)|large_intestine(26)|lung(57)|ovary(7)|pancreas(2)|prostate(1)|skin(3)|upper_aerodigestive_tract(4)|urinary_tract(4)	124				BRCA - Breast invasive adenocarcinoma(221;0.169)		CTCCGTGTTCGGATTGGTCAG	0.493												
MBD5	55777	broad.mit.edu	37	2	149248058	149248058	+	Silent	SNP	C	C	T			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:149248058C>T	uc002twm.4	+	11	5155	c.4158C>T	c.(4156-4158)ggC>ggT	p.G1386G	MBD5_uc010zbs.2_Intron|MBD5_uc002two.3_Silent_p.G644G|MBD5_uc002twp.3_Silent_p.G436G	NM_018328	NP_060798	Q9P267	MBD5_HUMAN	Homo sapiens methyl-CpG binding domain protein 5 (MBD5), mRNA.	1386	PWWP.					chromosome|nucleus	chromatin binding|DNA binding	p.G1386G(2)		NS(1)|breast(4)|central_nervous_system(1)|endometrium(8)|kidney(1)|large_intestine(16)|lung(22)|ovary(2)|prostate(1)|skin(3)|upper_aerodigestive_tract(3)	62				BRCA - Breast invasive adenocarcinoma(221;0.0569)		TCAATGTTGGCGACTTGGTCT	0.448												
SCN3A	6328	broad.mit.edu	37	2	166019113	166019113	+	Missense_Mutation	SNP	T	T	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:166019113T>A	uc002ucx.3	-	7	1412	c.920A>T	c.(919-921)aAt>aTt	p.N307I	SCN3A_uc002ucy.3_Missense_Mutation_p.N307I|SCN3A_uc002ucz.3_Missense_Mutation_p.N307I|SCN3A_uc002uda.1_Missense_Mutation_p.N176I|SCN3A_uc002udb.1_Missense_Mutation_p.N176I	NM_006922	NP_008853	Q9NY46	SCN3A_HUMAN	Homo sapiens sodium channel, voltage-gated, type III, alpha subunit (SCN3A), transcript variant 1, mRNA.	307						voltage-gated sodium channel complex	voltage-gated sodium channel activity			NS(1)|breast(7)|central_nervous_system(2)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(19)|liver(2)|lung(47)|ovary(6)|prostate(3)|skin(10)|upper_aerodigestive_tract(4)|urinary_tract(3)	120					Lamotrigine(DB00555)	CATTGTTACATTAACAAATGT	0.363												
SCN9A	6335	broad.mit.edu	37	2	167055670	167055670	+	Missense_Mutation	SNP	C	C	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:167055670C>A	uc010fpl.3	-	26	5787	c.5446G>T	c.(5446-5448)Gat>Tat	p.D1816Y	BC051759_uc002udp.3_Intron	NM_002977	NP_002968	Q15858	SCN9A_HUMAN	Homo sapiens sodium channel, voltage-gated, type IX, alpha subunit (SCN9A), mRNA.	1827						voltage-gated sodium channel complex	voltage-gated sodium channel activity			NS(1)|breast(5)|central_nervous_system(6)|endometrium(6)|kidney(3)|large_intestine(27)|lung(38)|ovary(6)|prostate(8)|skin(4)|upper_aerodigestive_tract(2)|urinary_tract(2)	108					Lamotrigine(DB00555)|Lidocaine(DB00281)	ATGGGCAGATCCATGGCAATG	0.463												
ZSWIM2	151112	broad.mit.edu	37	2	187693302	187693302	+	Silent	SNP	T	T	C			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:187693302T>C	uc002upu.1	-	8	1351	c.1311A>G	c.(1309-1311)agA>agG	p.R437R		NM_182521	NP_872327	Q8NEG5	ZSWM2_HUMAN	Homo sapiens zinc finger, SWIM-type containing 2 (ZSWIM2), mRNA.	437					apoptosis		zinc ion binding			cervix(1)|endometrium(1)|kidney(3)|large_intestine(6)|lung(28)|ovary(2)|prostate(4)|skin(6)|urinary_tract(1)	52			OV - Ovarian serous cystadenocarcinoma(117;0.0274)|Epithelial(96;0.164)			AAATTCCAAGTCTATTTTGTT	0.328												
ANO7	50636	broad.mit.edu	37	2	242151595	242151595	+	Missense_Mutation	SNP	G	G	A	rs111600763	byFrequency	TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr2:242151595G>A	uc002wax.2	+	15	1913	c.1810G>A	c.(1810-1812)Gtc>Atc	p.V604I		NM_001001891	NP_001001891	Q6IWH7	ANO7_HUMAN	Homo sapiens anoctamin 7 (ANO7), transcript variant NGEP-L, mRNA.	604						cell junction|chloride channel complex|cytosol	chloride channel activity			NS(1)|central_nervous_system(1)|endometrium(3)|large_intestine(5)|lung(14)|pancreas(2)|prostate(1)|skin(3)|urinary_tract(2)	32						CTCCTCACCCGTCTACATTGC	0.562												
SLC5A4	6527	broad.mit.edu	37	22	32627012	32627012	+	Missense_Mutation	SNP	C	C	G			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr22:32627012C>G	uc003ami.3	-	9	1074	c.1072G>C	c.(1072-1074)Gat>Cat	p.D358H		NM_014227	NP_055042	Q9NY91	SC5A4_HUMAN	Homo sapiens solute carrier family 5 (low affinity glucose cotransporter), member 4 (SLC5A4), mRNA.	358					carbohydrate transport|sodium ion transport	integral to membrane	symporter activity			NS(1)|breast(1)|central_nervous_system(1)|endometrium(2)|kidney(2)|large_intestine(6)|lung(15)|pancreas(2)|prostate(2)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	36						CAGCCAACATCAACGCCACAG	0.522												
CHL1	10752	broad.mit.edu	37	3	383663	383663	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr3:383663G>A	uc003bot.3	+	6	1219	c.577G>A	c.(577-579)Gtg>Atg	p.V193M	CHL1_uc003bou.3_Missense_Mutation_p.V193M|CHL1_uc003bow.2_Missense_Mutation_p.V193M|CHL1_uc011asi.2_Missense_Mutation_p.V193M	NM_006614	NP_006605	O00533	CHL1_HUMAN	Homo sapiens cell adhesion molecule with homology to L1CAM (close homolog of L1) (CHL1), transcript variant 1, mRNA.	193	Ig-like C2-type 2.				axon guidance|cell adhesion|signal transduction	integral to membrane|plasma membrane|proteinaceous extracellular matrix				NS(1)|central_nervous_system(5)|endometrium(11)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(25)|lung(31)|ovary(1)|prostate(4)|skin(10)|stomach(1)	93		all_cancers(2;1.14e-06)|all_epithelial(2;0.00367)|all_lung(1;0.061)|Lung NSC(2;0.201)		Epithelial(13;5.36e-06)|all cancers(10;1.4e-05)|OV - Ovarian serous cystadenocarcinoma(96;0.00323)|COAD - Colon adenocarcinoma(1;0.00925)|Colorectal(20;0.0198)		CTTCGCAAACGTGGAAGAAAA	0.383												
ZBTB20	26137	broad.mit.edu	37	3	114069362	114069362	+	Frame_Shift_Del	DEL	G	G	-			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr3:114069362delG	uc003ebi.3	-	3	1743	c.1563delC	c.(1561-1563)cccfs	p.P521fs	ZBTB20_uc003ebj.3_Frame_Shift_Del_p.P448fs|ZBTB20_uc010hqp.3_Frame_Shift_Del_p.P448fs|ZBTB20_uc003ebk.3_Frame_Shift_Del_p.P448fs|ZBTB20_uc003ebl.3_Frame_Shift_Del_p.P448fs|ZBTB20_uc003ebm.3_Frame_Shift_Del_p.P448fs|ZBTB20_uc003ebn.3_Frame_Shift_Del_p.P448fs|ZBTB20-AS1_uc003ebo.2_5'Flank	NM_001164342	NP_056457	Q9HC78	ZBT20_HUMAN	Homo sapiens zinc finger and BTB domain containing 20 (ZBTB20), transcript variant 1, mRNA.	521					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			breast(1)|central_nervous_system(1)|endometrium(10)|kidney(2)|large_intestine(8)|lung(15)|ovary(4)|pancreas(1)|prostate(1)|skin(3)|upper_aerodigestive_tract(2)	48				LUSC - Lung squamous cell carcinoma(41;0.0581)|Lung(219;0.191)		GGAAAGGCTTGGGGCCACTGC	0.627												
SPOCK3	50859	broad.mit.edu	37	4	167656159	167656159	+	Silent	SNP	A	A	G			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr4:167656159A>G	uc011cjq.1	-	9	1308	c.1251T>C	c.(1249-1251)atT>atC	p.I417I	SPOCK3_uc021xuf.1_Silent_p.I408I|SPOCK3_uc011cjr.1_Silent_p.I288I|SPOCK3_uc003iri.1_Silent_p.I408I|SPOCK3_uc011cjs.1_Silent_p.I357I|SPOCK3_uc003irj.1_Silent_p.I405I|SPOCK3_uc011cjt.1_Silent_p.I316I|SPOCK3_uc011cjp.2_Silent_p.I365I|SPOCK3_uc011cju.1_Silent_p.I312I|SPOCK3_uc011cjv.1_Silent_p.I310I	NM_001204353	NP_001191282	Q9BQ16	TICN3_HUMAN	Homo sapiens sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 3 (SPOCK3), transcript variant 4, mRNA.	408	Asp-rich.				signal transduction	proteinaceous extracellular matrix	calcium ion binding|metalloendopeptidase inhibitor activity			NS(2)|breast(1)|central_nervous_system(1)|endometrium(4)|kidney(1)|large_intestine(9)|lung(13)|ovary(1)|prostate(1)|skin(4)|upper_aerodigestive_tract(1)	38	all_hematologic(180;0.221)	Prostate(90;0.0181)|Renal(120;0.0184)|Melanoma(52;0.0198)		GBM - Glioblastoma multiforme(119;0.02)		catcattcataatatcgtctt	0.363												
FSTL4	23105	broad.mit.edu	37	5	132556518	132556518	+	Silent	SNP	G	G	A	rs141735817	byFrequency	TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr5:132556518G>A	uc003kyn.1	-	11	1598	c.1380C>T	c.(1378-1380)gaC>gaT	p.D460D	FSTL4_uc003kym.1_Silent_p.D109D	NM_015082	NP_055897	Q6MZW2	FSTL4_HUMAN	Homo sapiens follistatin-like 4 (FSTL4), mRNA.	460						extracellular region	calcium ion binding			autonomic_ganglia(1)|breast(2)|central_nervous_system(1)|endometrium(1)|kidney(3)|large_intestine(4)|lung(8)|skin(2)|upper_aerodigestive_tract(1)	23		all_cancers(142;0.244)	KIRC - Kidney renal clear cell carcinoma(527;0.0186)|Kidney(363;0.0365)			CGATGATACCGTCGTCGGAGA	0.547												
PCDHAC2	9752	broad.mit.edu	37	5	140229589	140229589	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr5:140229589G>A	uc003lhu.2	+	0	2233	c.1509G>A	c.(1507-1509)tcG>tcA	p.S503S	PCDHAC2_uc003lha.2_Intron|PCDHAC2_uc003lhb.2_Intron|PCDHAC2_uc003lhd.2_Intron|PCDHAC2_uc003lhf.2_Intron|PCDHAC2_uc003lhh.1_Intron|PCDHAC2_uc003lhi.2_Intron|PCDHAC2_uc003lhl.2_Intron|PCDHAC2_uc003lhk.1_Intron|PCDHAC2_uc003lho.2_Intron|PCDHAC2_uc003lhn.2_Intron|PCDHAC2_uc003lhq.2_Intron|PCDHAC2_uc003lhs.2_Intron|PCDHAC2_uc003lht.1_Silent_p.S503S	NM_031857	NP_114063	Q9Y5I4	PCDC2_HUMAN	Homo sapiens protocadherin alpha 9 (PCDHA9), transcript variant 1, mRNA.	517	Cadherin 5.				homophilic cell adhesion|nervous system development	integral to plasma membrane	calcium ion binding	p.S503S(2)		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)			GCGAGCGCTCGCTGTCGAGCT	0.672												
LAMB1	3912	broad.mit.edu	37	7	107591684	107591684	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr7:107591684G>A	uc003vev.2	-	21	3611	c.3450C>T	c.(3448-3450)gaC>gaT	p.D1150D	LAMB1_uc003vew.2_Silent_p.D1126D	NM_002291	NP_002282	P07942	LAMB1_HUMAN	Homo sapiens laminin, beta 1 (LAMB1), mRNA.	1126	Laminin EGF-like 13.				axon guidance|odontogenesis|positive regulation of cell migration|positive regulation of epithelial cell proliferation|substrate adhesion-dependent cell spreading	extracellular space|laminin-1 complex|laminin-10 complex|laminin-2 complex|laminin-8 complex|perinuclear region of cytoplasm	extracellular matrix structural constituent			NS(3)|breast(1)|central_nervous_system(2)|cervix(1)|endometrium(4)|kidney(4)|large_intestine(11)|lung(37)|ovary(6)|prostate(5)|skin(5)|upper_aerodigestive_tract(3)	82					Alteplase(DB00009)|Anistreplase(DB00029)|Reteplase(DB00015)|Tenecteplase(DB00031)	GGCACTCCACGTCGGGGTCTC	0.572												
SGK223	157285	broad.mit.edu	37	8	8175745	8175745	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr8:8175745G>A	uc003wsh.4	-	4	4140	c.4140C>T	c.(4138-4140)tgC>tgT	p.C1380C		NM_001080826	NP_001074295	Q86YV5	SG223_HUMAN	Homo sapiens homolog of rat pragma of Rnd2 (SGK223), mRNA.	1380							ATP binding|non-membrane spanning protein tyrosine kinase activity										GGTACTGGCAGCAAAGCCAGT	0.642												
PIP5K1B	8395	broad.mit.edu	37	9	71555697	71555697	+	Missense_Mutation	SNP	A	A	C			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr9:71555697A>C	uc004agu.3	+	13	1798	c.1493A>C	c.(1492-1494)tAt>tCt	p.Y498S	PIP5K1B_uc011lrq.2_Missense_Mutation_p.Y498S|PIP5K1B_uc004agv.3_Non-coding_Transcript	NM_003558	NP_003549	O14986	PI51B_HUMAN	Homo sapiens phosphatidylinositol-4-phosphate 5-kinase, type I, beta (PIP5K1B), transcript variant 2, mRNA.	498						endomembrane system|membrane|uropod	1-phosphatidylinositol-4-phosphate 5-kinase activity|ATP binding|protein binding			breast(1)|large_intestine(2)|stomach(1)	4				Lung(182;0.133)		CCTACACTCTATTCAAACAGG	0.443												
SUSD1	64420	broad.mit.edu	37	9	114840947	114840947	+	Missense_Mutation	SNP	T	T	C			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chr9:114840947T>C	uc010mui.3	-	11	1665	c.1624A>G	c.(1624-1626)Aat>Gat	p.N542D	MIR3134_uc022bma.1_Intron|SUSD1_uc004bfu.3_Missense_Mutation_p.N542D|SUSD1_uc010muj.3_Missense_Mutation_p.N542D			Q6UWL2	SUSD1_HUMAN	Homo sapiens sushi domain containing 1 (SUSD1), mRNA.	542						integral to membrane	calcium ion binding		SUSD1/ROD1(2)	central_nervous_system(1)|endometrium(4)|large_intestine(8)|lung(11)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)	28						CTACTGATATTAAAGGTCATT	0.488												
CXorf59	286464	broad.mit.edu	37	X	36103467	36103467	+	Silent	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chrX:36103467G>A	uc004ddk.1	+	4	639	c.453G>A	c.(451-453)tcG>tcA	p.S151S		NM_173695	NP_775966	Q8N9S7	CX059_HUMAN	Homo sapiens chromosome X open reading frame 59 (CXorf59), mRNA.	151						integral to membrane		p.S151S(2)		breast(2)|central_nervous_system(2)|endometrium(2)|large_intestine(7)|lung(18)|skin(1)|upper_aerodigestive_tract(2)	34						CATCAACCTCGCCACCCCAAA	0.333												
DCAF12L2	340578	broad.mit.edu	37	X	125299499	125299499	+	Missense_Mutation	SNP	G	G	A			TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chrX:125299499G>A	uc004euk.2	-	0	582	c.409C>T	c.(409-411)Cgg>Tgg	p.R137W		NM_001013628	NP_001013650	Q5VW00	DC122_HUMAN	Homo sapiens DDB1 and CUL4 associated factor 12-like 2 (DCAF12L2), mRNA.	137										NS(2)|central_nervous_system(1)|cervix(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(11)|lung(36)|ovary(2)|pancreas(1)|skin(2)|upper_aerodigestive_tract(3)	64						TCCTTGTCCCGCATGAGGGGG	0.642												
OR13H1	347468	broad.mit.edu	37	X	130678349	130678349	+	Missense_Mutation	SNP	C	C	T	rs149527425	byFrequency	TCGA-06-0132-01A-02D-1491-08	TCGA-06-0132-10A-01D-1491-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	53c2e159-5774-499f-b0d1-e04fa3faf5c3	740f8d17-3563-4a13-8089-509a5989c33d	g.chrX:130678349C>T	uc011muw.2	+	0	302	c.302C>T	c.(301-303)aCg>aTg	p.T101M	IGSF1_uc004ewf.2_Intron	NM_001004486	NP_001004486	Q8NG92	O13H1_HUMAN	Homo sapiens olfactory receptor, family 13, subfamily H, member 1 (OR13H1), mRNA.	101					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			endometrium(3)|large_intestine(3)|lung(7)|prostate(1)|skin(1)	15	Acute lymphoblastic leukemia(192;0.000636)					TTGGCTCAAACGAGTGTCTCC	0.517												
