Hugo_Symbol	Entrez_Gene_Id	Center	NCBI_Build	Chromosome	Start_position	End_position	Strand	Variant_Classification	Variant_Type	Reference_Allele	Tumor_Seq_Allele1	Tumor_Seq_Allele2	dbSNP_RS	dbSNP_Val_Status	Tumor_Sample_Barcode	Matched_Norm_Sample_Barcode	Match_Norm_Seq_Allele1	Match_Norm_Seq_Allele2	Tumor_Validation_Allele1	Tumor_Validation_Allele2	Match_Norm_Validation_Allele1	Match_Norm_Validation_Allele2	Verification_Status	Validation_Status	Mutation_Status	Sequencing_Phase	Sequence_Source	Validation_Method	Score	BAM_file	Sequencer	Tumor_Sample_UUID	Matched_Norm_Sample_UUID	Genome_Change	Annotation_Transcript	Transcript_Strand	Transcript_Exon	Transcript_Position	cDNA_Change	Codon_Change	Protein_Change	Other_Transcripts	Refseq_mRNA_Id	Refseq_prot_Id	SwissProt_acc_Id	SwissProt_entry_Id	Description	UniProt_AApos	UniProt_Region	UniProt_Site	UniProt_Natural_Variations	UniProt_Experimental_Info	GO_Biological_Process	GO_Cellular_Component	GO_Molecular_Function	COSMIC_overlapping_mutations	COSMIC_fusion_genes	COSMIC_tissue_types_affected	COSMIC_total_alterations_in_gene	Tumorscape_Amplification_Peaks	Tumorscape_Deletion_Peaks	TCGAscape_Amplification_Peaks	TCGAscape_Deletion_Peaks	DrugBank	ref_context	gc_content	CCLE_ONCOMAP_overlapping_mutations	CCLE_ONCOMAP_total_mutations_in_gene	CGC_Mutation_Type	CGC_Translocation_Partner	CGC_Tumor_Types_Somatic	CGC_Tumor_Types_Germline	CGC_Other_Diseases	DNARepairGenes_Role	FamilialCancerDatabase_Syndromes	MUTSIG_Published_Results	OREGANNO_ID	OREGANNO_Values	t_alt_count	t_ref_count	validation_alt_allele	validation_method	validation_status	validation_tumor_sample	pox	qox	pox_cutoff	isArtifactMode	oxoGCut
CDK5R2	8941	broad.mit.edu	37	2	219825271	219825271	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr2:219825271C>T	uc002vjf.3	+	0	874	c.729C>T	c.(727-729)tgC>tgT	p.C243C		NM_003936	NP_003927	Q13319	CD5R2_HUMAN	Homo sapiens cyclin-dependent kinase 5, regulatory subunit 2 (p39) (CDK5R2), mRNA.	243					regulation of cyclin-dependent protein kinase activity	cyclin-dependent protein kinase 5 holoenzyme complex	cyclin-dependent protein kinase 5 activator activity			central_nervous_system(2)|endometrium(2)|large_intestine(2)|lung(1)|ovary(1)	8		Renal(207;0.0474)		Epithelial(149;9.77e-07)|all cancers(144;0.000167)|LUSC - Lung squamous cell carcinoma(224;0.008)|Lung(261;0.00942)		ACCTGCTGTGCCGCGAGTCGC	0.662000													5	227					0	0	1	0	0
CDH7	1005	broad.mit.edu	37	18	63477082	63477082	+	Missense_Mutation	SNP	A	A	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr18:63477082A>G	uc002lkb.3	+	2	779	c.353A>G	c.(352-354)tAc>tGc	p.Y118C	CDH7_uc002ljz.3_Missense_Mutation_p.Y118C|CDH7_uc002lka.3_Missense_Mutation_p.Y118C	NM_004361	NP_387450	Q9ULB5	CADH7_HUMAN	Homo sapiens cadherin 7, type 2 (CDH7), transcript variant b, mRNA.	118	Cadherin 1.				adherens junction organization|cell junction assembly|homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding	p.Y118H(1)		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)				CAGGCCTACTACACGCTCCGA	0.502000													3	73					0	0	1	0	0
FRG1B	284802	broad.mit.edu	37	20	29625947	29625947	+	Missense_Mutation	SNP	T	T	C			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr20:29625947T>C	uc010ztl.1	+	1	133	c.101T>C	c.(100-102)aTt>aCt	p.I34T	FRG1B_uc002wvm.1_Non-coding_Transcript|FRG1B_uc010ztj.1_Non-coding_Transcript|FRG1B_uc010gdr.1_Non-coding_Transcript|FRG1B_uc010ztk.1_Intron					Homo sapiens FSHD region gene 1 family, member B (FRG1B), non-coding RNA.									p.I64T(4)		endometrium(10)|kidney(21)|lung(3)|pancreas(1)|prostate(9)|urinary_tract(9)	53						TCAGATGCAATTGGACCAAGA	0.343000													5	104					0	0	1	0	0
GOT2	2806	broad.mit.edu	37	16	58743428	58743428	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr16:58743428G>A	uc002eof.1	-	8	1177	c.1063C>T	c.(1063-1065)Cgg>Tgg	p.R355W	GOT2_uc010vim.1_Missense_Mutation_p.R312W	NM_002080	NP_002071	P00505	AATM_HUMAN	Homo sapiens glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2) (GOT2), nuclear gene encoding mitochondrial protein, mRNA.	355					aspartate catabolic process|fatty acid transport|gluconeogenesis|response to ethanol	mitochondrial matrix|plasma membrane	L-aspartate:2-oxoglutarate aminotransferase activity|protein binding|pyridoxal phosphate binding	p.R355W(4)|p.R355G(2)		breast(1)|central_nervous_system(1)|cervix(1)|endometrium(3)|kidney(3)|large_intestine(2)|lung(8)|prostate(2)|skin(1)	22					L-Aspartic Acid(DB00128)|L-Glutamic Acid(DB00142)|Pyridoxal Phosphate(DB00114)	AGTTGAGTCCGCATGCCAATG	0.507000													5	324					0	0	1	0	0
OBSCN	84033	broad.mit.edu	37	1	228466419	228466419	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:228466419C>T	uc009xez.1	+	25	6933	c.6889C>T	c.(6889-6891)Cgg>Tgg	p.R2297W	OBSCN_uc001hsn.3_Missense_Mutation_p.R2297W|OBSCN_uc001hsp.1_5'UTR|OBSCN_uc001hsq.1_5'Flank	NM_001098623	NP_001092093	Q5VST9	OBSCN_HUMAN	Homo sapiens obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF (OBSCN), transcript variant 2, mRNA.	2297	Ig-like 23.				apoptosis|cell differentiation|induction of apoptosis by extracellular signals|multicellular organismal development|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction	M band|Z disc|cytosol	ATP binding|Rho guanyl-nucleotide exchange factor activity|metal ion binding|protein binding|protein serine/threonine kinase activity|protein tyrosine kinase activity|structural constituent of muscle|titin binding			NS(2)|breast(7)|central_nervous_system(5)|cervix(2)|endometrium(30)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(37)|lung(89)|ovary(8)|pancreas(3)|prostate(13)|skin(6)|stomach(11)|upper_aerodigestive_tract(2)|urinary_tract(3)	223		Prostate(94;0.0405)				GCGCCCGCTGCGGGACAAGAT	0.662000													5	79					0	0	1	0	0
PET112	5188	broad.mit.edu	37	4	152592397	152592397	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr4:152592397G>A	uc003iml.3	-	12	1644	c.1603C>T	c.(1603-1605)Cgg>Tgg	p.R535W	PET112_uc003imk.3_Non-coding_Transcript	NM_004564	NP_004555	O75879	GATB_HUMAN	Homo sapiens PET112 homolog (yeast) (PET112), nuclear gene encoding mitochondrial protein, mRNA.	535						mitochondrion	ATP binding|carbon-nitrogen ligase activity, with glutamine as amido-N-donor|translation factor activity, nucleic acid binding			breast(1)|endometrium(5)|kidney(1)|large_intestine(7)|lung(5)|ovary(1)|prostate(1)|upper_aerodigestive_tract(2)	23					L-Glutamic Acid(DB00142)|L-Glutamine(DB00130)	GTCGCTTTCCGGACCAACCCA	0.448000													7	120					0	0	1	0	0
RNF135	84282	broad.mit.edu	37	17	29325769	29325769	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr17:29325769C>T	uc002hfz.3	+	4	995	c.859C>T	c.(859-861)Cca>Tca	p.P287S	RNF135_uc010csm.3_3'UTR|RNF135_uc002hga.3_3'UTR|RNF135_uc002hgb.3_3'UTR	NM_032322	NP_115698	Q8IUD6	RN135_HUMAN	Homo sapiens ring finger protein 135 (RNF135), transcript variant 1, mRNA.	287	B30.2/SPRY.				innate immune response|negative regulation of type I interferon production|positive regulation of interferon-beta production|regulation of innate immune response	cytosol	protein binding|ribonucleoprotein binding|ubiquitin-protein ligase activity|zinc ion binding	p.R286H(1)|p.?(1)		breast(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(2)|large_intestine(2)|lung(1)|skin(2)|urinary_tract(1)	10		all_cancers(10;8.65e-08)|all_hematologic(16;0.00556)|Acute lymphoblastic leukemia(14;0.00593)|Myeloproliferative disorder(56;0.0255)				GTCTCACCGCCCACAACCCTA	0.522000													6	87					0	0	1	0	0
MRPS10	55173	broad.mit.edu	37	6	42176031	42176031	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr6:42176031G>A	uc003osa.4	-	6	648	c.602C>T	c.(601-603)tCa>tTa	p.S201L	MRPS10_uc011dup.2_Missense_Mutation_p.S160L	NM_018141	NP_060611	P82664	RT10_HUMAN	Homo sapiens mitochondrial ribosomal protein S10 (MRPS10), nuclear gene encoding mitochondrial protein, mRNA.	201					translation	actin cytoskeleton|mitochondrion|ribosome	structural constituent of ribosome			endometrium(1)|lung(1)	2	Colorectal(47;0.196)		Colorectal(64;0.00062)|COAD - Colon adenocarcinoma(64;0.00152)|Epithelial(12;0.00528)			GAGGCTTTATGACTTGCTTTC	0.393000													10	324					0	0	1	0	0
PRKD1	5587	broad.mit.edu	37	14	30100144	30100144	+	Silent	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr14:30100144G>A	uc001wqh.3	-	9	1657	c.1476C>T	c.(1474-1476)ttC>ttT	p.F492F	MIR548AI_uc021rrv.1_Intron	NM_002742	NP_002733	Q15139	KPCD1_HUMAN	Homo sapiens protein kinase D1 (PRKD1), mRNA.	492	PH.				cell proliferation|intracellular signal transduction|sphingolipid metabolic process	cytosol|integral to plasma membrane	ATP binding|metal ion binding|protein binding|protein kinase C activity			NS(1)|breast(2)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(21)|lung(32)|ovary(2)|prostate(1)|skin(4)|urinary_tract(2)	78	Hepatocellular(127;0.0604)		LUAD - Lung adenocarcinoma(48;0.00527)|Lung(238;0.0252)	GBM - Glioblastoma multiforme(265;0.00888)		TAGTGATTTCGAAACAATGAG	0.398000													6	88					0	0	1	0	0
PCDHAC2	56134	broad.mit.edu	37	5	140215658	140215658	+	Missense_Mutation	SNP	G	G	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr5:140215658G>T	uc003lhq.2	+	0	1690	c.1690G>T	c.(1690-1692)Gca>Tca	p.A564S	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_uc011dac.2_Missense_Mutation_p.A564S	NM_018910	NP_061733	Q9Y5I4	PCDC2_HUMAN	Homo sapiens protocadherin alpha 7 (PCDHA7), transcript variant 1, mRNA.	578	Cadherin 5.				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)			CAACGCGCCGGCACTGCTGGC	0.687000													19	184					0	0	1	0	0
FSCN3	29999	broad.mit.edu	37	7	127235472	127235472	+	Missense_Mutation	SNP	C	C	T	rs146886586		TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr7:127235472C>T	uc003vmd.2	+	1	475	c.256C>T	c.(256-258)Cgc>Tgc	p.R86C	FSCN3_uc003vmc.1_Missense_Mutation_p.R41C|FSCN3_uc011kog.1_Non-coding_Transcript|FSCN3_uc011koh.1_5'UTR|FSCN3_uc010llc.2_Missense_Mutation_p.R86C	NM_020369	NP_065102	Q9NQT6	FSCN3_HUMAN	Homo sapiens fascin homolog 3, actin-bundling protein, testicular (Strongylocentrotus purpuratus) (FSCN3), mRNA.	86						actin cytoskeleton|cytoplasm	actin filament binding|protein binding, bridging			endometrium(2)|large_intestine(3)|liver(2)|lung(17)|ovary(2)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)	30						GTGTTATGGCCGCCCAAGGAC	0.562000													8	72					0	0	1	0	0
ANKRD20A9P	284232	broad.mit.edu	37	13	19414170	19414170	+	RNA	SNP	T	T	C			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr13:19414170T>C	uc010tcj.1	-	0		c.31940A>G								Homo sapiens ankyrin repeat domain 20 family, member A9, pseudogene (ANKRD20A9P), non-coding RNA.																		GATTGAACAGTTGGTTCAAGT	0.269000													3	33					0	0	1	0	0
R3HDM1	23518	broad.mit.edu	37	2	136481598	136481598	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr2:136481598C>T	uc002tuo.3	+	25	3406	c.3036C>T	c.(3034-3036)ggC>ggT	p.G1012G	R3HDM1_uc010fni.3_Silent_p.G1011G|R3HDM1_uc002tup.3_Silent_p.G957G|R3HDM1_uc010zbh.2_Silent_p.G760G	NM_015361	NP_056176	Q15032	R3HD1_HUMAN	Homo sapiens R3H domain containing 1 (R3HDM1), mRNA.	1012							nucleic acid binding			breast(2)|endometrium(6)|kidney(5)|large_intestine(3)|lung(14)|pancreas(1)|prostate(1)|skin(2)|stomach(1)|urinary_tract(3)	38				BRCA - Breast invasive adenocarcinoma(221;0.127)		TTAAAATTGGCGCCAAGATCC	0.517000													4	110					0	0	1	0	0
OR8K1	390157	broad.mit.edu	37	11	56113902	56113902	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr11:56113902G>A	uc010rjg.2	+	0	388	c.388G>A	c.(388-390)Gta>Ata	p.V130I		NM_001002907	NP_001002907	Q8NGG5	OR8K1_HUMAN	Homo sapiens olfactory receptor, family 8, subfamily K, member 1 (OR8K1), mRNA.	130					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity	p.V130I(2)		large_intestine(8)|liver(2)|lung(13)|ovary(1)|pancreas(1)|prostate(2)|skin(2)|upper_aerodigestive_tract(3)|urinary_tract(1)	33	Esophageal squamous(21;0.00448)					TGATCGCTACGTAGCCATCTG	0.413000										HNSCC(65;0.19)			10	196					0	0	1	0	0
TIAM2	26230	broad.mit.edu	37	6	155561701	155561701	+	Missense_Mutation	SNP	A	A	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr6:155561701A>T	uc003qqb.3	+	17	4479	c.3206A>T	c.(3205-3207)aAc>aTc	p.N1069I	TIAM2_uc003qqe.3_Missense_Mutation_p.N1069I|TIAM2_uc010kjj.3_Missense_Mutation_p.N602I|TIAM2_uc003qqf.3_Missense_Mutation_p.N445I|TIAM2_uc011efl.1_Missense_Mutation_p.N405I|TIAM2_uc003qqg.3_Missense_Mutation_p.N381I|TIAM2_uc003qqh.3_5'UTR	NM_012454	NP_036586	Q8IVF5	TIAM2_HUMAN	Homo sapiens T-cell lymphoma invasion and metastasis 2 (TIAM2), transcript variant 1, mRNA.	1069					apoptosis|cellular lipid metabolic process|induction of apoptosis by extracellular signals|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction	cytosol|filopodium|growth cone|lamellipodium	Rho guanyl-nucleotide exchange factor activity|receptor signaling protein activity			breast(2)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(20)|lung(21)|ovary(5)|prostate(1)|skin(2)|upper_aerodigestive_tract(4)	65		Ovarian(120;0.196)		OV - Ovarian serous cystadenocarcinoma(155;8.1e-13)|BRCA - Breast invasive adenocarcinoma(81;0.0053)		AGGAGTTTTAACGACAGTCAG	0.582000													5	53					0	0	1	0	0
EGR3	1960	broad.mit.edu	37	8	22548994	22548994	+	Splice_Site	SNP	C	C	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr8:22548994C>G	uc003xcm.1	-	2	513	c.155_splice	c.e2-1	p.E52_splice	EGR3_uc011kzn.1_Splice_Site_p.E14_splice|EGR3_uc011kzo.2_Splice_Site	NM_004430	NP_001186810	Q06889	EGR3_HUMAN	Homo sapiens early growth response 3 (EGR3), transcript variant 1, mRNA.	52					circadian rhythm|muscle organ development	nucleus	DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding			breast(1)|endometrium(1)|large_intestine(2)|lung(4)|upper_aerodigestive_tract(1)|urinary_tract(1)	10		Prostate(55;0.0421)|Breast(100;0.102)		Colorectal(74;0.0145)|BRCA - Breast invasive adenocarcinoma(99;0.053)|COAD - Colon adenocarcinoma(73;0.0608)		CCATTACATTCTCTGCGGAGA	0.667000													5	103					0	0	1	0	0
MLLT3	4300	broad.mit.edu	37	9	20414346	20414346	+	Silent	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr9:20414346G>A	uc003zoe.2	-	4	757	c.498C>T	c.(496-498)agC>agT	p.S166S	MLLT3_uc011lne.1_Silent_p.S134S|MLLT3_uc011lnf.1_Silent_p.S163S|MLLT3_uc003zof.3_5'UTR	NM_004529	NP_004520	P42568	AF9_HUMAN	Homo sapiens myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3 (MLLT3), mRNA.	166	Poly-Ser.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	protein binding	p.S166S(8)		central_nervous_system(1)|cervix(1)|endometrium(13)|haematopoietic_and_lymphoid_tissue(1)|kidney(7)|large_intestine(6)|lung(24)|ovary(1)|prostate(4)|skin(1)|urinary_tract(7)	66				GBM - Glioblastoma multiforme(3;4.35e-105)|Lung(42;3.48e-06)|LUSC - Lung squamous cell carcinoma(42;7.92e-05)		tgctgctactgctgctgctgc	0.527000			T	MLL	ALL								4	52					0	0	1	0	0
KIF3C	3797	broad.mit.edu	37	2	26203359	26203359	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr2:26203359C>T	uc002rgu.2	-	0	2085	c.1428G>A	c.(1426-1428)caG>caA	p.Q476Q	KIF3C_uc010eyj.1_Non-coding_Transcript|KIF3C_uc010ykr.1_Silent_p.Q476Q	NM_002254	NP_002245	O14782	KIF3C_HUMAN	Homo sapiens kinesin family member 3C (KIF3C), mRNA.	476					blood coagulation|microtubule-based movement	cytosol|kinesin complex|microtubule	ATP binding|microtubule motor activity			breast(3)|central_nervous_system(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(5)|lung(8)|ovary(4)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	29	Acute lymphoblastic leukemia(172;0.155)|all_hematologic(175;0.215)					TGCGGTCATCCTGGATGGCTG	0.617000													6	123					0	0	1	0	0
KLHDC7A	127707	broad.mit.edu	37	1	18807930	18807930	+	Missense_Mutation	SNP	A	A	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:18807930A>G	uc001bax.3	+	0	507	c.455A>G	c.(454-456)aAc>aGc	p.N152S	KLHDC7A_uc009vpg.3_5'UTR	NM_152375	NP_689588	Q5VTJ3	KLD7A_HUMAN	Homo sapiens kelch domain containing 7A (KLHDC7A), mRNA.	152						integral to membrane				endometrium(1)|kidney(1)|large_intestine(4)|lung(11)|ovary(2)|skin(1)|upper_aerodigestive_tract(2)	22		Colorectal(325;3.46e-05)|all_lung(284;0.000152)|Lung NSC(340;0.000185)|Breast(348;0.00046)|Renal(390;0.000518)|Ovarian(437;0.0014)|Myeloproliferative disorder(586;0.0255)		UCEC - Uterine corpus endometrioid carcinoma (279;0.00462)|BRCA - Breast invasive adenocarcinoma(304;1.41e-05)|Kidney(64;0.00017)|KIRC - Kidney renal clear cell carcinoma(64;0.00258)|STAD - Stomach adenocarcinoma(196;0.00644)|READ - Rectum adenocarcinoma(331;0.0649)		GTTGGCAGTAACCCTGACCCT	0.647000													4	71					0	0	1	0	0
MDM1	56890	broad.mit.edu	37	12	68710032	68710032	+	Splice_Site	SNP	A	A	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr12:68710032A>G	uc001stz.2	-	8	1142	c.1006_splice	c.e8-1	p.V336_splice	MDM1_uc009zqv.1_Splice_Site_p.V56_splice|MDM1_uc010stc.1_Splice_Site_p.V301_splice	NM_017440	NP_059136	Q8TC05	MDM1_HUMAN	Homo sapiens Mdm1 nuclear protein homolog (mouse) (MDM1), transcript variant 1, mRNA.	336						nucleus				breast(1)|endometrium(4)|kidney(1)|large_intestine(4)|lung(10)|ovary(3)|pancreas(1)|prostate(2)|skin(7)	33			Lung(24;0.000131)|LUAD - Lung adenocarcinoma(15;0.00107)|STAD - Stomach adenocarcinoma(21;0.018)	GBM - Glioblastoma multiforme(7;0.000174)		GAGTTCTTTAACCTATTCAGG	0.403000													3	36					0	0	1	0	0
C6orf70	55780	broad.mit.edu	37	6	170162587	170162587	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr6:170162587C>T	uc003qxg.1	+	8	953	c.920C>T	c.(919-921)gCc>gTc	p.A307V	C6orf70_uc011ehb.1_Missense_Mutation_p.A181V|C6orf70_uc003qxh.1_Missense_Mutation_p.A307V|C6orf70_uc010kky.1_Missense_Mutation_p.A181V	NM_018341	NP_060811	Q5T6L9	CF070_HUMAN	Homo sapiens chromosome 6 open reading frame 70 (C6orf70), mRNA.	307						integral to membrane				breast(1)|endometrium(1)|kidney(3)|large_intestine(7)|lung(7)|ovary(1)	20		Breast(66;5.08e-05)|Ovarian(120;0.208)		OV - Ovarian serous cystadenocarcinoma(33;1.2e-22)|BRCA - Breast invasive adenocarcinoma(81;1.49e-07)|GBM - Glioblastoma multiforme(31;0.00191)		AATGTTTTTGCCACACTTAAC	0.383000													4	134					0	0	1	0	0
MYLK	4638	broad.mit.edu	37	3	123383037	123383037	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr3:123383037C>T	uc003ego.3	-	22	4182	c.3900G>A	c.(3898-3900)gcG>gcA	p.A1300A	MYLK_uc010hrr.3_5'UTR|MYLK_uc011bjv.2_Silent_p.A100A|MYLK_uc011bjw.2_Silent_p.A1300A|MYLK_uc003egp.3_Silent_p.A1231A|MYLK_uc003egq.3_Silent_p.A1300A|MYLK_uc003egr.3_Silent_p.A1231A|MYLK_uc003egs.3_Silent_p.A1124A	NM_053025	NP_444253	Q15746	MYLK_HUMAN	Homo sapiens myosin light chain kinase (MYLK), transcript variant 1, mRNA.	1300	Actin-binding (calcium/calmodulin- insensitive) (By similarity).|Ig-like C2-type 8.			A -> G (in Ref. 1; CAA59685).	aorta smooth muscle tissue morphogenesis|muscle contraction	cytosol	ATP binding|actin binding|calmodulin binding|metal ion binding|myosin light chain kinase activity			NS(2)|breast(4)|central_nervous_system(1)|endometrium(24)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(17)|lung(37)|ovary(7)|prostate(3)|skin(5)|stomach(1)|upper_aerodigestive_tract(5)|urinary_tract(2)	113		Lung NSC(201;0.0496)		GBM - Glioblastoma multiforme(114;0.0736)		GCTCCTGGCGCGCGGCCAGGA	0.627000													23	216					0	0	1	0	0
KLK8	11202	broad.mit.edu	37	19	51499377	51499377	+	Missense_Mutation	SNP	C	C	T	rs56296296	byFrequency	TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr19:51499377C>T	uc002puq.1	-	5	1042	c.856G>A	c.(856-858)Gtc>Atc	p.V286I	KLK8_uc002pur.1_Missense_Mutation_p.V241I|KLK8_uc002pus.1_Missense_Mutation_p.V100I|KLK8_uc002put.1_3'UTR|KLK8_uc002puu.1_Missense_Mutation_p.V241I|KLK8_uc002puv.1_Non-coding_Transcript	NM_144505	NP_653088	O60259	KLK8_HUMAN	Homo sapiens kallikrein-related peptidase 8 (KLK8), transcript variant 2, mRNA.	241					cell death|keratinocyte proliferation|memory|negative regulation of axon regeneration|negative regulation of myelination|neuron projection morphogenesis|proteolysis|regulation of synapse organization|response to wounding	cytoplasm|extracellular space	protein binding|serine-type endopeptidase activity	p.V286I(2)		central_nervous_system(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|lung(8)|prostate(1)	15		all_neural(266;0.026)		OV - Ovarian serous cystadenocarcinoma(262;0.0033)|GBM - Glioblastoma multiforme(134;0.00888)		TTGGTATAGACGCCAGGTTTG	0.542000													4	174					0	0	1	0	0
PRRC2B	84726	broad.mit.edu	37	9	134366823	134366823	+	Silent	SNP	A	A	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr9:134366823A>T	uc004can.4	+	27	6292	c.6237A>T	c.(6235-6237)ccA>ccT	p.P2079P	PRRC2B_uc004cao.4_Silent_p.P1436P|PRRC2B_uc004cap.4_Silent_p.P225P|PRRC2B_uc011mch.2_Silent_p.P2P	NM_013318	NP_037450	Q5JSZ5	PRC2B_HUMAN	Homo sapiens proline-rich coiled-coil 2B (PRRC2B), mRNA.	2079							protein binding			cervix(2)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(7)|lung(20)|ovary(2)	44						TGACCATGCCACTGCCTCGGT	0.612000													12	105					0	0	1	0	0
abParts	0	broad.mit.edu	37	22	22663087	22663087	+	RNA	SNP	A	A	G	rs1054158		TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr22:22663087A>G	uc021wml.1	+	30		c.2445A>G			abParts_uc011aiq.1_Non-coding_Transcript|abParts_uc011aip.2_Non-coding_Transcript|abParts_uc010gto.3_Non-coding_Transcript					Parts of antibodies, mostly variable regions.																		GCTGCCACATAAGTTGTCCTT	0.303000													5	36					0	0	1	0	0
PARG	8505	broad.mit.edu	37	10	51093329	51093329	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr10:51093329C>T	uc001jih.3	-	8	1891	c.1750G>A	c.(1750-1752)Gca>Aca	p.A584T	PARG_uc009xoj.3_Missense_Mutation_p.A135T|PARG_uc001jif.3_Missense_Mutation_p.A584T|PARG_uc001jig.3_Missense_Mutation_p.A170T|PARG_uc010qgv.2_Intron|PARG_uc009xoi.3_Intron|PARG_uc010qgw.2_Missense_Mutation_p.A475T|PARG_uc010qgx.2_Missense_Mutation_p.A502T	NM_003631	NP_003622	Q86W56	PARG_HUMAN	Homo sapiens poly (ADP-ribose) glycohydrolase (PARG), mRNA.	584					carbohydrate metabolic process	nucleus	poly(ADP-ribose) glycohydrolase activity	p.A584T(2)		endometrium(5)|kidney(2)|lung(1)|ovary(2)	10				Epithelial(53;0.213)		TGAGCTTCTGCTTCTTCAAGT	0.318000													4	52					0	0	1	0	0
HM13	81502	broad.mit.edu	37	20	30115327	30115327	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr20:30115327C>T	uc002wwc.3	+	1	338	c.224C>T	c.(223-225)gCc>gTc	p.A75V	HM13_uc002wwd.3_Missense_Mutation_p.A75V|HM13_uc002wwe.3_Missense_Mutation_p.A75V|HM13_uc002wwb.1_Missense_Mutation_p.A75V	NM_178581	NP_848696	Q8TCT9	HM13_HUMAN	Homo sapiens histocompatibility (minor) 13 (HM13), transcript variant 3, mRNA.	75					membrane protein proteolysis	cell surface|endoplasmic reticulum membrane|integral to membrane|plasma membrane	aspartic-type endopeptidase activity|protein binding			breast(1)|endometrium(2)|large_intestine(2)|lung(4)|prostate(1)|skin(1)|urinary_tract(1)	12	all_cancers(5;3.44e-05)|Lung NSC(7;4.38e-06)|all_lung(7;7.65e-06)|all_hematologic(12;0.158)|Ovarian(7;0.198)		all cancers(5;0.000479)|Colorectal(19;0.00202)|COAD - Colon adenocarcinoma(19;0.0264)			AGCCGGGATGCCGCCCGCTTC	0.502000													4	163					0	0	1	0	0
TBP	6908	broad.mit.edu	37	6	170871043	170871043	+	Silent	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr6:170871043G>A	uc003qxu.3	+	2	498	c.219G>A	c.(217-219)caG>caA	p.Q73Q	TBP_uc011ehf.2_Silent_p.Q53Q|TBP_uc003qxt.3_Silent_p.Q73Q|TBP_uc011ehg.1_Silent_p.Q73Q	NM_003194	NP_001165556	P20226	TBP_HUMAN	Homo sapiens TATA box binding protein (TBP), transcript variant 1, mRNA.	73	Poly-Gln.				cell death|interspecies interaction between organisms|transcription elongation from RNA polymerase II promoter|transcription from RNA polymerase III promoter|viral reproduction	transcription factor TFIIA complex|transcription factor TFIID complex	repressing transcription factor binding|transcription regulatory region DNA binding	p.Q72del(3)|p.Q73Q(2)		breast(2)|central_nervous_system(1)|endometrium(5)|kidney(1)|large_intestine(2)|lung(9)|ovary(1)|prostate(4)|urinary_tract(1)	26		Breast(66;5.08e-05)|Ovarian(120;0.125)|Esophageal squamous(34;0.246)		OV - Ovarian serous cystadenocarcinoma(33;1.07e-22)|BRCA - Breast invasive adenocarcinoma(81;5.01e-06)|GBM - Glioblastoma multiforme(31;0.00591)		agcagcaacagcaacagcagc	0.562000													5	50					0	0	1	0	0
MUC1	4582	broad.mit.edu	37	1	155161799	155161799	+	Missense_Mutation	SNP	T	T	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:155161799T>G	uc021pap.1	-	1	433	c.361A>C	c.(361-363)Acc>Ccc	p.T121P	MUC1_uc001fhz.3_5'Flank|MUC1_uc001fhy.3_5'Flank|MUC1_uc010pfb.2_Intron|MUC1_uc010pfh.2_Intron|MUC1_uc010pff.2_Intron|MUC1_uc010pfi.2_Intron|MUC1_uc010pfj.2_Intron|MUC1_uc010pfk.2_Intron|MUC1_uc010pfl.2_Intron|MUC1_uc010pfc.2_Intron|MUC1_uc009wph.3_Intron|MUC1_uc010pfe.2_Intron|MUC1_uc009wpi.3_Intron|MUC1_uc010pfg.2_Intron|MUC1_uc010pfd.2_Intron|MUC1_uc009wpy.3_Intron|MUC1_uc009wpu.3_Intron|MUC1_uc010pfm.2_Intron|MUC1_uc001fiq.3_Intron|MUC1_uc009wqa.3_Intron|MUC1_uc010pfn.2_Intron|MUC1_uc009wpn.3_Intron|MUC1_uc010pfo.2_Intron|MUC1_uc009wpw.3_Intron|MUC1_uc001fim.3_Intron|MUC1_uc001fil.3_Intron|MUC1_uc010pfp.2_Intron|MUC1_uc001fij.3_Intron|MUC1_uc009wqc.3_Intron|MUC1_uc009wqd.3_Intron|MUC1_uc001fia.3_Intron|MUC1_uc009wqb.3_Intron|MUC1_uc009wpx.3_Intron|MUC1_uc010pfq.2_Intron|MUC1_uc001fid.3_Intron|MUC1_uc001fit.3_Intron|MUC1_uc009wpz.3_Intron|MUC1_uc001fii.3_Intron|MUC1_uc001fik.3_Intron|MUC1_uc009wpo.3_Intron|MUC1_uc010pfr.2_Intron|MUC1_uc001fih.3_Intron|MUC1_uc001fio.3_Intron|MUC1_uc009wqe.3_Intron|MUC1_uc009wpl.3_Intron|MUC1_uc009wpp.3_Intron|MUC1_uc009wpm.3_Intron|MUC1_uc009wpk.3_Intron|MUC1_uc010pfs.2_Intron|MUC1_uc001fip.3_Intron|MUC1_uc021paq.1_Missense_Mutation_p.T112P|MUC1_uc009wqg.3_Intron|MUC1_uc009wqf.3_Intron|MUC1_uc001fic.3_Intron|MUC1_uc009wps.3_Intron|MUC1_uc001fie.3_Intron|MUC1_uc009wpt.3_Intron|MUC1_uc009wpq.3_Intron|MUC1_uc009wpr.3_Intron|MUC1_uc001fig.3_Intron|MUC1_uc001fif.3_Intron|MUC1_uc001fin.3_Intron|MUC1_uc009wpj.3_Intron|MUC1_uc009wpv.3_Intron|MUC1_uc001fib.3_Intron|MUC1_uc001fis.2_Intron|MUC1_uc001fiv.2_Missense_Mutation_p.T121P|MUC1_uc001fiw.2_Missense_Mutation_p.T112P|DM075093_uc021par.1_5'Flank	NM_001204286	NP_001191215	P15941	MUC1_HUMAN	Homo sapiens mucin 1, cell surface associated (MUC1), transcript variant 10, mRNA.	892						apical plasma membrane|cell surface|cytoplasm|extracellular region|integral to plasma membrane|nucleus	protein binding			breast(1)|kidney(1)|large_intestine(1)|lung(3)|ovary(1)|pancreas(1)|skin(2)	10	all_epithelial(22;5.72e-28)|all_lung(78;2.07e-24)|all_hematologic(923;0.0359)|Hepatocellular(266;0.0877)		Epithelial(20;5.31e-10)|all cancers(21;2.19e-09)|BRCA - Breast invasive adenocarcinoma(34;0.000752)|LUSC - Lung squamous cell carcinoma(543;0.193)			GCTGGCGGGGTGGTGGAGCCC	0.711000			T	IGH@	B-NHL								8	19					0	0	1	0	0
SETDB1	9869	broad.mit.edu	37	1	150936826	150936826	+	Missense_Mutation	SNP	G	G	C			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:150936826G>C	uc001evu.2	+	21	4052	c.3862G>C	c.(3862-3864)Gga>Cga	p.G1288R	SETDB1_uc001evv.2_Missense_Mutation_p.G1287R	NM_001145415	NP_001138887	Q15047	SETB1_HUMAN	Homo sapiens SET domain, bifurcated 1 (SETDB1), transcript variant 1, mRNA.	1288	Post-SET.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	Golgi apparatus|chromosome|nucleus|plasma membrane	DNA binding|histone-lysine N-methyltransferase activity|protein binding|zinc ion binding			NS(1)|large_intestine(5)|ovary(3)|skin(2)|upper_aerodigestive_tract(1)	12	all_lung(15;9e-35)|Lung NSC(24;3.45e-31)|Lung SC(34;0.00471)|Ovarian(49;0.0167)|all_hematologic(923;0.0597)|Hepatocellular(266;0.108)|Melanoma(130;0.185)		UCEC - Uterine corpus endometrioid carcinoma (35;0.0486)|BRCA - Breast invasive adenocarcinoma(12;0.0152)|LUSC - Lung squamous cell carcinoma(543;0.211)			TGAATGCAGAGGACGTCTTCT	0.522000													6	23					0	0	1	0	0
ZNF783	100289678	broad.mit.edu	37	7	148979001	148979001	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr7:148979001G>A	uc011kuo.2	+	5	1371	c.1208G>A	c.(1207-1209)gGc>gAc	p.G403D	AF035281_uc003wfr.4_Intron	NM_001195220	NP_001182149	C9J9J2	C9J9J2_HUMAN	Homo sapiens zinc finger family member 783 (ZNF783), mRNA.	403					regulation of transcription, DNA-dependent	intracellular	nucleic acid binding|zinc ion binding			cervix(1)|endometrium(2)|kidney(2)|large_intestine(6)|lung(10)|prostate(1)	22	Melanoma(164;0.15)		OV - Ovarian serous cystadenocarcinoma(82;0.0014)			GTGGTACCCGGCCCTGTCATC	0.746000													3	18					0	0	1	0	0
PKD1	5310	broad.mit.edu	37	16	2142146	2142146	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr16:2142146C>T	uc002cos.1	-	39	11522	c.11313G>A	c.(11311-11313)tcG>tcA	p.S3771S	TCRBV20S1_uc021tak.1_Intron|PKD1_uc002cot.1_Silent_p.S3770S|MIR1225_uc021tap.1_5'Flank|PKD1_uc010bse.1_Non-coding_Transcript	NM_001009944	NP_001009944	P98161	PKD1_HUMAN	Homo sapiens polycystic kidney disease 1 (autosomal dominant) (PKD1), transcript variant 1, mRNA.	3771					calcium-independent cell-matrix adhesion|homophilic cell adhesion|neuropeptide signaling pathway	basolateral plasma membrane|integral to plasma membrane	protein domain specific binding|sugar binding			breast(1)|central_nervous_system(3)|cervix(1)|endometrium(7)|kidney(6)|lung(34)|prostate(4)|skin(10)|upper_aerodigestive_tract(3)|urinary_tract(3)	72						CTCCTGCGGCCGAGCACGTGT	0.647000													7	32					0	0	1	0	0
SCN5A	6331	broad.mit.edu	37	3	38627374	38627374	+	Silent	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr3:38627374G>A	uc021wvo.1	-	14	2647	c.2595C>T	c.(2593-2595)taC>taT	p.Y865Y	SCN5A_uc021wvk.1_Silent_p.Y865Y|SCN5A_uc021wvl.1_Silent_p.Y865Y|SCN5A_uc021wvm.1_Silent_p.Y865Y|SCN5A_uc021wvn.1_Silent_p.Y865Y|SCN5A_uc021wvp.1_Silent_p.Y865Y|SCN5A_uc021wvq.1_Silent_p.Y865Y|SCN5A_uc021wvr.1_Silent_p.Y865Y|SCN5A_uc021wvs.1_Silent_p.Y865Y|SCN5A_uc021wvt.1_Silent_p.Y865Y|SCN5A_uc021wvu.1_Silent_p.Y865Y|SCN5A_uc021wvv.1_Silent_p.Y865Y|SCN5A_uc021wvj.1_Silent_p.Y731Y|SCN5A_uc021wvi.1_Silent_p.Y731Y|SCN5A_uc021wvw.1_Silent_p.Y476Y	NM_198056	NP_932173	Q14524	SCN5A_HUMAN	Homo sapiens sodium channel, voltage-gated, type V, alpha subunit (SCN5A), transcript variant 1, mRNA.	865					blood circulation|cellular response to calcium ion|muscle contraction|regulation of heart contraction	sarcolemma|voltage-gated sodium channel complex	protein binding|voltage-gated sodium channel activity			NS(3)|breast(2)|central_nervous_system(3)|cervix(2)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(25)|lung(27)|ovary(6)|pancreas(3)|prostate(10)|skin(9)|upper_aerodigestive_tract(4)	107	Medulloblastoma(35;0.163)			KIRC - Kidney renal clear cell carcinoma(284;0.0822)|Kidney(284;0.1)	Benzonatate(DB00868)|Bepridil(DB01244)|Carbamazepine(DB00564)|Cocaine(DB00907)|Dibucaine(DB00527)|Disopyramide(DB00280)|Encainide(DB01228)|Ethotoin(DB00754)|Flecainide(DB01195)|Fosphenytoin(DB01320)|Hexylcaine(DB00473)|Indecainide(DB00192)|Lamotrigine(DB00555)|Lidocaine(DB00281)|Mephenytoin(DB00532)|Mexiletine(DB00379)|Mibefradil(DB01388)|Moricizine(DB00680)|Oxcarbazepine(DB00776)|Phenytoin(DB00252)|Prilocaine(DB00750)|Procainamide(DB01035)|Propafenone(DB01182)|Quinidine(DB00908)|Riluzole(DB00740)|Tocainide(DB01056)|Verapamil(DB00661)	TCAGCTCCGAGTAGTTCTTGC	0.562000													9	127					0	0	1	0	0
TBP	6908	broad.mit.edu	37	6	170871082	170871082	+	Silent	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr6:170871082G>A	uc003qxu.3	+	2	537	c.258G>A	c.(256-258)caG>caA	p.Q86Q	TBP_uc011ehf.2_Silent_p.Q66Q|TBP_uc003qxt.3_Silent_p.Q86Q|TBP_uc011ehg.1_Silent_p.Q86Q	NM_003194	NP_001165556	P20226	TBP_HUMAN	Homo sapiens TATA box binding protein (TBP), transcript variant 1, mRNA.	86	Poly-Gln.				cell death|interspecies interaction between organisms|transcription elongation from RNA polymerase II promoter|transcription from RNA polymerase III promoter|viral reproduction	transcription factor TFIIA complex|transcription factor TFIID complex	repressing transcription factor binding|transcription regulatory region DNA binding	p.Q86Q(4)		breast(2)|central_nervous_system(1)|endometrium(5)|kidney(1)|large_intestine(2)|lung(9)|ovary(1)|prostate(4)|urinary_tract(1)	26		Breast(66;5.08e-05)|Ovarian(120;0.125)|Esophageal squamous(34;0.246)		OV - Ovarian serous cystadenocarcinoma(33;1.07e-22)|BRCA - Breast invasive adenocarcinoma(81;5.01e-06)|GBM - Glioblastoma multiforme(31;0.00591)		agcagcagcagcagcagcagc	0.612000													5	46					0	0	1	0	0
TTC18	118491	broad.mit.edu	37	10	75104854	75104854	+	Missense_Mutation	SNP	A	A	G			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr10:75104854A>G	uc009xrc.3	-	5	699	c.578T>C	c.(577-579)aTg>aCg	p.M193T	TTC18_uc001jty.3_Missense_Mutation_p.M193T|TTC18_uc009xrd.1_Missense_Mutation_p.M1T	NM_145170	NP_660153	Q5T0N1	TTC18_HUMAN	Homo sapiens tetratricopeptide repeat domain 18 (TTC18), mRNA.	193							binding			breast(1)|central_nervous_system(1)|endometrium(2)|kidney(2)|large_intestine(6)|lung(13)|ovary(2)|prostate(2)|stomach(3)|upper_aerodigestive_tract(1)|urinary_tract(1)	34	Prostate(51;0.0119)					CAGACCGACCATGTAGTTCTG	0.488000													22	247					0	0	1	0	0
CD200R1L	344807	broad.mit.edu	37	3	112546303	112546303	+	Missense_Mutation	SNP	G	G	A			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr3:112546303G>A	uc003dzi.1	-	2	567	c.341C>T	c.(340-342)cCg>cTg	p.P114L	CD200R1L_uc010hqf.1_Missense_Mutation_p.P93L|CD200R1L_uc011bhw.1_Missense_Mutation_p.P93L	NM_001008784	NP_001186144	Q6Q8B3	MO2R2_HUMAN	Homo sapiens CD200 receptor 1-like (CD200R1L), transcript variant 1, mRNA.	114	Ig-like V-type.					integral to membrane	receptor activity			breast(2)|central_nervous_system(1)|endometrium(1)|large_intestine(4)|lung(6)|ovary(1)|prostate(2)|urinary_tract(2)	19						GGTGTCCACCGGACGAATCTG	0.453000													5	81					0	0	1	0	0
SLCO4A1	28231	broad.mit.edu	37	20	61288286	61288286	+	Silent	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr20:61288286C>T	uc002ydb.1	+	1	685	c.480C>T	c.(478-480)gtC>gtT	p.V160V		NM_016354	NP_057438	Q96BD0	SO4A1_HUMAN	Homo sapiens solute carrier organic anion transporter family, member 4A1 (SLCO4A1), mRNA.	160					sodium-independent organic anion transport	integral to membrane|plasma membrane	thyroid hormone transmembrane transporter activity			endometrium(6)|kidney(2)|large_intestine(1)|lung(7)|ovary(3)|prostate(2)	21	Breast(26;3.65e-08)		BRCA - Breast invasive adenocarcinoma(19;2.33e-06)			TCACCTTCGTCAGCTACTTCG	0.667000													9	73					0	0	1	0	0
SF3B1	23451	broad.mit.edu	37	2	198265579	198265579	+	Missense_Mutation	SNP	C	C	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr2:198265579C>T	uc002uue.3	-	17	2626	c.2578G>A	c.(2578-2580)Gaa>Aaa	p.E860K	SNORD2_uc021vul.1_5'Flank	NM_012433	NP_036565	O75533	SF3B1_HUMAN	Homo sapiens splicing factor 3b, subunit 1, 155kDa (SF3B1), transcript variant 1, mRNA.	860					nuclear mRNA splicing, via spliceosome	U12-type spliceosomal complex|catalytic step 2 spliceosome|nuclear speck	protein binding			NS(35)|breast(10)|central_nervous_system(3)|endometrium(8)|haematopoietic_and_lymphoid_tissue(524)|kidney(4)|large_intestine(10)|lung(19)|ovary(1)|pancreas(4)|prostate(6)|salivary_gland(1)|skin(4)|testis(1)|upper_aerodigestive_tract(1)|urinary_tract(2)	633			OV - Ovarian serous cystadenocarcinoma(117;0.246)			TGTTCGGCTTCATCTTTCAGA	0.363000			Mis		myelodysplastic syndrome								14	67					0	0	1	0	0
TMEM52	339456	broad.mit.edu	37	1	1850628	1850636	+	In_Frame_Del	DEL	AGCGGCAGG	AGCGGCAGG	-			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:1850628_1850636delAGCGGCAGG	uc001aij.2	-	0	105_113	c.69_77delCCTGCCGCT	c.(67-78)ctcctgccgctg>ctg	p.23_26LLPL>L	TMEM52_uc001aii.2_5'Flank	NM_178545	NP_848640	Q8NDY8	TMM52_HUMAN	Homo sapiens transmembrane protein 52 (TMEM52), mRNA.	23						integral to membrane				NS(1)|prostate(1)|stomach(1)	3	all_cancers(77;0.000708)|all_epithelial(69;0.000943)|all_lung(157;0.00963)|Lung NSC(156;0.0232)|Ovarian(185;0.0634)	all_epithelial(116;6.04e-15)|all_lung(118;9.67e-07)|Lung NSC(185;5.59e-05)|Renal(390;0.00571)|Breast(487;0.0183)|Hepatocellular(190;0.0268)|Myeloproliferative disorder(586;0.028)|Ovarian(437;0.127)|Medulloblastoma(700;0.151)|Lung SC(97;0.217)		Epithelial(90;1.82e-37)|OV - Ovarian serous cystadenocarcinoma(86;2.75e-23)|GBM - Glioblastoma multiforme(42;9e-08)|Colorectal(212;3.94e-05)|COAD - Colon adenocarcinoma(227;0.000193)|Kidney(185;0.00227)|BRCA - Breast invasive adenocarcinoma(365;0.00435)|STAD - Stomach adenocarcinoma(132;0.00644)|KIRC - Kidney renal clear cell carcinoma(229;0.0339)|Lung(427;0.199)		CACCTgcggcagcggcaggagcggcagga	0.766													2	4	---	---	---	---					
MST1P2	11209	broad.mit.edu	37	1	16974141	16974141	+	RNA	DEL	G	G	-			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr1:16974141delG	uc009vow.2	+	4		c.951delG			CROCCP2_uc001azg.1_5'Flank|CROCCP2_uc001azi.1_5'Flank|MST1P2_uc010ocg.1_Non-coding_Transcript|MST1P2_uc010och.2_Intron|MST1P2_uc010oci.1_Non-coding_Transcript|MST1P2_uc001azk.2_Intron|MST1P2_uc009vox.3_Intron|MST1P2_uc001azm.4_Intron					Homo sapiens macrophage stimulating 1 (hepatocyte growth factor-like) pseudogene 2 (MST1P2), non-coding RNA.																		TGGCTTGGCCGGGGAGGTCAG	0.667													3	6	---	---	---	---					
SAMD9L	219285	broad.mit.edu	37	7	92760915	92760916	+	Frame_Shift_Ins	INS	-	-	T			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr7:92760915_92760916insT	uc003umh.1	-	4	5585_5586	c.4369_4370insA	c.(4369-4371)agafs	p.R1457fs	SAMD9L_uc003umj.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc003umi.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc010lfb.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc003umk.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc010lfc.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc010lfd.1_Frame_Shift_Ins_p.R1457fs|SAMD9L_uc022ahh.1_Frame_Shift_Ins_p.R1457fs	NM_152703	NP_689916	Q8IVG5	SAM9L_HUMAN	Homo sapiens sterile alpha motif domain containing 9-like (SAMD9L), mRNA.	1457										central_nervous_system(1)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(23)|liver(2)|lung(31)|ovary(5)|prostate(2)|skin(6)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(4)	88	all_cancers(62;4.15e-11)|all_epithelial(64;2.29e-10)|Breast(17;0.000675)|Lung NSC(181;0.0755)|all_lung(186;0.0989)		STAD - Stomach adenocarcinoma(171;0.000302)			CCTGAAGGATCTATTTAAGGAT	0.436													9	173	---	---	---	---					
CALD1	800	broad.mit.edu	37	7	134618474	134618476	+	In_Frame_Del	DEL	GGA	GGA	-			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr7:134618474_134618476delGGA	uc003vrz.3	+	4	1420_1422	c.954_956delGGA	c.(952-957)agggag>agg	p.E321del	CALD1_uc003vry.3_Intron|CALD1_uc003vsb.3_Intron|CALD1_uc011kpt.2_Intron|CALD1_uc010lmm.3_Intron|CALD1_uc003vsc.3_Intron|CALD1_uc003vsd.3_Intron|CALD1_uc011kpu.2_Intron|CALD1_uc011kpv.2_Intron|CALD1_uc003vse.3_In_Frame_Del_p.E185del	NM_033138	NP_149129	Q05682	CALD1_HUMAN	Homo sapiens caldesmon 1 (CALD1), transcript variant 1, mRNA.	321	3 X 14 AA tandem repeats of E-E-E-K-R-A- A-E-E-R-Q-R-I-K.				cellular component movement|muscle contraction	cytosol|focal adhesion|myofibril	actin binding|calmodulin binding|myosin binding|tropomyosin binding			NS(1)|autonomic_ganglia(1)|breast(4)|central_nervous_system(2)|cervix(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(2)|kidney(4)|large_intestine(15)|lung(10)	43						aaaggatgagggaggaagagaaa	0.483													3	5	---	---	---	---					
LOC390660	390660	broad.mit.edu	37	15	82620383	82620384	+	RNA	INS	-	-	ACCCAGG			TCGA-G9-6347-01A-11D-A31L-08	TCGA-G9-6347-10A-01D-A31J-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	470a25cd-eea8-4ca6-b91c-86e36397135a	b63236ea-caa8-44c1-ba56-d36c6c394c23	g.chr15:82620383_82620384insACCCAGG	uc021ssl.1	+	18		c.3863_3864insACCCAGG			LOC390660_uc010bls.1_Non-coding_Transcript					Homo sapiens FLJ00317 protein (LOC390660), non-coding RNA.																		GCCTGCCCTGAACCCAGGACCC	0.663													7	10	---	---	---	---					
