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
RTN2	6253	broad.mit.edu	37	19	45998115	45998115	+	Silent	SNP	C	C	G			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr19:45998115C>G	ENST00000245923.4	-	3	463	c.228G>C	c.(226-228)ggG>ggC	p.G76G	RTN2_ENST00000589384.1_5'UTR|RTN2_ENST00000590526.1_5'UTR|RTN2_ENST00000344680.4_Silent_p.G76G|PPM1N_ENST00000401705.1_Intron	NM_005619.4	NP_005610.1	O75298	RTN2_HUMAN	reticulon 2	76						integral to endoplasmic reticulum membrane	signal transducer activity			cervix(1)|endometrium(2)|kidney(3)|large_intestine(2)|lung(6)|ovary(4)|skin(1)|urinary_tract(1)	20		Ovarian(192;0.051)|all_neural(266;0.112)		OV - Ovarian serous cystadenocarcinoma(262;0.00829)|Epithelial(262;0.184)|GBM - Glioblastoma multiforme(486;0.246)		CCCTGCGGCCCCCGGAGCCCA	0.687000													13	20					0	0	1	0	0
HSF5	124535	broad.mit.edu	37	17	56557351	56557351	+	Silent	SNP	T	T	C			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr17:56557351T>C	ENST00000323777.3	-	2	937	c.828A>G	c.(826-828)gtA>gtG	p.V276V		NM_001080439.1	NP_001073908.1	Q4G112	HSF5_HUMAN	heat shock transcription factor family member 5	276						nucleus	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity			endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(3)|lung(7)|ovary(3)|skin(1)	16	Medulloblastoma(34;0.127)|all_neural(34;0.237)					GTTGAACATGTACAGATGTGG	0.468000													37	60					0	0	1	0	0
ZNF733P	0	broad.mit.edu	37	7	62752443	62752443	+	RNA	SNP	G	G	C			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr7:62752443G>C	ENST00000331425.6	-	0	992					NR_003952.1																						CTTATGTCTAGTAAGGTTTGA	0.438000													5	13					0	0	1	0	0
DEAF1	10522	broad.mit.edu	37	11	694809	694809	+	Missense_Mutation	SNP	G	G	C			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr11:694809G>C	ENST00000382409.3	-	1	723	c.239C>G	c.(238-240)gCc>gGc	p.A80G	DEAF1_ENST00000338675.6_Missense_Mutation_p.A80G	NM_021008.2	NP_066288.2	O75398	DEAF1_HUMAN	DEAF1 transcription factor	80	Ala-rich.				embryonic skeletal system development|germ cell development|neural tube closure|regulation of mammary gland epithelial cell proliferation|regulation of transcription, DNA-dependent|transcription from RNA polymerase II promoter	cytoplasm|extracellular region|nucleus	protein binding|zinc ion binding			breast(2)|endometrium(3)|kidney(1)|large_intestine(4)|lung(11)|prostate(2)|upper_aerodigestive_tract(1)	24		all_cancers(49;1.24e-08)|all_epithelial(84;1.87e-05)|Breast(177;0.000286)|Ovarian(85;0.000953)|Medulloblastoma(188;0.0109)|all_neural(188;0.0299)|Lung NSC(207;0.106)|all_lung(207;0.136)		all cancers(45;1.76e-27)|Epithelial(43;8.42e-27)|OV - Ovarian serous cystadenocarcinoma(40;6.55e-21)|BRCA - Breast invasive adenocarcinoma(625;4.83e-05)|Lung(200;0.0259)|LUSC - Lung squamous cell carcinoma(625;0.075)		CAGGGCCTCGGCGCCCATGTC	0.771000													4	1					0	0	1	0	0
MUTYH	4595	broad.mit.edu	37	1	45797891	45797891	+	Missense_Mutation	SNP	G	G	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr1:45797891G>A	ENST00000450313.1	-	10	1095	c.880C>T	c.(880-882)Cgc>Tgc	p.R294C	MUTYH_ENST00000528332.2_Intron|MUTYH_ENST00000354383.6_Missense_Mutation_p.R267C|MUTYH_ENST00000355498.2_Missense_Mutation_p.R266C|MUTYH_ENST00000372110.3_Missense_Mutation_p.R281C|MUTYH_ENST00000448481.1_Missense_Mutation_p.R277C|MUTYH_ENST00000372115.3_Missense_Mutation_p.R280C|MUTYH_ENST00000456914.2_Missense_Mutation_p.R266C|MUTYH_ENST00000372100.5_Missense_Mutation_p.R277C|MUTYH_ENST00000531105.1_Intron|MUTYH_ENST00000372098.3_Missense_Mutation_p.R291C|MUTYH_ENST00000529984.1_Intron|MUTYH_ENST00000488731.2_Intron|MUTYH_ENST00000372104.1_Missense_Mutation_p.R266C	NM_001128425.1|NM_012222.2	NP_001121897.1|NP_036354.1	Q9UIF7	MUTYH_HUMAN	mutY homolog	291					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)					CACAGTGGGCGCTGTGGGGTA	0.617000			Mis			colorectal		Base excision repair (BER), DNA glycosylases	MUTYH-associated polyposis				3	36					0	0	1	0	0
MT-TL1	0	broad.mit.edu	37	MT	3244	3244	+	RNA	SNP	G	G	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chrM:3244G>A	ENST00000386347.1	+	0	15																											aagatggcagagcccggtaat	0.438000													7	1					0	0	1	0	0
ZNF580	51157	broad.mit.edu	37	19	56153895	56153895	+	Silent	SNP	G	G	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr19:56153895G>A	ENST00000543039.1	+	1	478	c.21G>A	c.(19-21)cgG>cgA	p.R7R	ZNF581_ENST00000587252.1_Intron|ZNF580_ENST00000545125.1_Silent_p.R7R|ZNF580_ENST00000325333.5_Silent_p.R7R	NM_016202.2	NP_057286.1	Q9UK33	ZN580_HUMAN	zinc finger protein 580	7	Pro-rich.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			lung(1)|upper_aerodigestive_tract(1)	2			BRCA - Breast invasive adenocarcinoma(297;0.18)	GBM - Glioblastoma multiforme(193;0.105)		TGCCGCCGCGGCCACCCCACC	0.627000													3	17					0	0	1	0	0
DISP1	84976	broad.mit.edu	37	1	223176363	223176363	+	Missense_Mutation	SNP	T	T	G			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr1:223176363T>G	ENST00000284476.6	+	8	1788	c.1624T>G	c.(1624-1626)Tcc>Gcc	p.S542A		NM_032890.3	NP_116279.2	Q96F81	DISP1_HUMAN	dispatched homolog 1 (Drosophila)	542	SSD.				diaphragm development|protein homotrimerization|regulation of protein secretion|smoothened signaling pathway	basolateral plasma membrane|integral to membrane	hedgehog receptor activity|peptide transporter activity			breast(1)|central_nervous_system(1)|cervix(1)|endometrium(7)|kidney(3)|large_intestine(20)|lung(25)|prostate(4)|skin(1)|stomach(1)|urinary_tract(5)	69				GBM - Glioblastoma multiforme(131;0.102)		TTTGATTGTTTCCTATTTTCT	0.353000													21	43					0	0	1	0	0
BNC2	54796	broad.mit.edu	37	9	16435992	16435992	+	Missense_Mutation	SNP	C	C	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr9:16435992C>A	ENST00000380672.4	-	6	2257	c.2200G>T	c.(2200-2202)Ggc>Tgc	p.G734C	BNC2_ENST00000545497.1_Missense_Mutation_p.G639C|BNC2_ENST00000380666.2_Missense_Mutation_p.G734C|BNC2_ENST00000380667.2_Missense_Mutation_p.G667C	NM_017637.5	NP_060107.3	Q6ZN30	BNC2_HUMAN	basonuclin 2	734					regulation of transcription, DNA-dependent|transcription, DNA-dependent	cytoplasm|nucleus|plasma membrane	zinc ion binding			NS(2)|breast(3)|central_nervous_system(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(16)|liver(1)|lung(22)|ovary(2)|prostate(1)|skin(1)|urinary_tract(2)	60				GBM - Glioblastoma multiforme(50;9.01e-08)		GATTCCTCGCCCAGTTTGGGC	0.512000													7	44					0.307466	0.307466	1	1	0
ZRSR1	7310	broad.mit.edu	37	5	112227939	112227939	+	Silent	SNP	T	T	C	rs712666	by1000genomes	TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr5:112227939T>C	ENST00000391338.1	+	1	627	c.603T>C	c.(601-603)tcT>tcC	p.S201S	REEP5_ENST00000379638.4_Intron|REEP5_ENST00000504247.1_Intron|REEP5_ENST00000513339.1_Intron|SRP19_ENST00000512790.1_3'UTR|REEP5_ENST00000474542.2_Intron|REEP5_ENST00000545426.1_Intron	NM_001204199.1	NP_001191128.1			zinc finger (CCCH type), RNA-binding motif and serine/arginine rich 1									p.S201S(1)		breast(1)|skin(1)|stomach(2)	4						TCCCAACATCTAGTCCTACCC	0.453000													4	77					0	0	1	0	0
ADCK2	90956	broad.mit.edu	37	7	140394532	140394532	+	Silent	SNP	C	C	T			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr7:140394532C>T	ENST00000072869.4	+	8	1988	c.1810C>T	c.(1810-1812)Ctg>Ttg	p.L604L	ADCK2_ENST00000476491.1_Intron|NDUFB2_ENST00000482954.1_Intron	NM_052853.3	NP_443085.2	Q7Z695	ADCK2_HUMAN	aarF domain containing kinase 2	604	Protein kinase.					integral to membrane	ATP binding|protein serine/threonine kinase activity			cervix(1)|kidney(2)|large_intestine(2)|lung(5)|prostate(1)|skin(4)	15	Melanoma(164;0.00956)					TGGCCGCTCACTGGACCCCAA	0.582000													19	44					0	0	1	0	0
TSSC2	0	broad.mit.edu	37	11	3427845	3427845	+	RNA	SNP	C	C	T			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr11:3427845C>T	ENST00000529482.1	+	0	962																											CTTCAAGTGGCAGGAGCAGAA	0.587000													4	24					0	0	1	0	0
TRIOBP	11078	broad.mit.edu	37	22	38120673	38120673	+	Missense_Mutation	SNP	G	G	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr22:38120673G>A	ENST00000406386.3	+	7	2365	c.2110G>A	c.(2110-2112)Gac>Aac	p.D704N	RP1-37E16.12_ENST00000455236.1_RNA	NM_001039141.2	NP_001034230.1	Q9H2D6	TARA_HUMAN	TRIO and F-actin binding protein	704					actin modification|barbed-end actin filament capping	actin cytoskeleton|cytoplasm|nucleus	actin binding|GTP-Rho binding|myosin II binding|protein binding|ubiquitin protein ligase binding			central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(1)|lung(3)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	12	Melanoma(58;0.0574)					TGCCCAACGGGACGATCCCAG	0.582000													13	48					0	0	1	0	0
GNPAT	8443	broad.mit.edu	37	1	231411174	231411174	+	Missense_Mutation	SNP	T	T	A			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr1:231411174T>A	ENST00000366647.4	+	14	2036	c.1867T>A	c.(1867-1869)Tta>Ata	p.L623I	GNPAT_ENST00000366646.3_Missense_Mutation_p.L562I|GNPAT_ENST00000469332.1_3'UTR	NM_014236.3	NP_055051.1	O15228	GNPAT_HUMAN	glyceronephosphate O-acyltransferase	623					ether lipid biosynthetic process|fatty acid metabolic process|organ morphogenesis	peroxisomal matrix|peroxisomal membrane	glycerone-phosphate O-acyltransferase activity	p.L623V(1)		breast(2)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(2)|lung(9)|ovary(3)|prostate(1)|skin(1)	23	Breast(184;0.0871)	all_cancers(173;0.2)|Prostate(94;0.183)				TTATGATGTATTATCTTCTGA	0.428000													4	61					0	0	1	0	0
BRAF	673	broad.mit.edu	37	7	140453136	140453136	+	Missense_Mutation	SNP	A	A	T	rs121913377		TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr7:140453136A>T	ENST00000288602.6	-	15	1859	c.1799T>A	c.(1798-1800)gTg>gAg	p.V600E		NM_004333.4	NP_004324.2	P15056	BRAF_HUMAN	v-raf murine sarcoma viral oncogene homolog B	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(15453)|p.V600K(252)|p.V600R(44)|p.V600D(16)|p.V600A(12)|p.V600_K601>E(12)|p.V600G(11)|p.T599_R603>I(2)|p.V600Q(2)|p.V600_S605>EK(1)|p.V600_S605>DV(1)|p.V600_S605>D(1)|p.T599_V600insDFGLAT(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	0.368000	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				21	42					0	0	1	0	0
FEZF1-AS1	0	broad.mit.edu	37	7	121944603	121944605	+	RNA	DEL	CCT	CCT	-			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr7:121944603_121944605delCCT	ENST00000428449.1	+	0	611					NR_036484.1																						CCACCAGTAGcctcctcctcctc	0.655													2	4	---	---	---	---					
FANCG	2189	broad.mit.edu	37	9	35079179	35079179	+	Frame_Shift_Del	DEL	T	T	-			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr9:35079179delT	ENST00000378643.3	-	2	635	c.144delA	c.(142-144)gafs	p.E48fs		NM_004629.1	NP_004620.1	O15287	FANCG_HUMAN	Fanconi anemia, complementation group G	48					cell cycle checkpoint|DNA repair|mitochondrion organization	mitochondrion|nucleoplasm	damaged DNA binding|protein binding			NS(1)|breast(1)|endometrium(3)|kidney(3)|large_intestine(7)|lung(7)|ovary(2)|prostate(3)|stomach(1)	28			LUSC - Lung squamous cell carcinoma(32;0.00343)|Lung(28;0.00778)			CTCTGAGCCCTTCCAGTGCAT	0.582			"""Mis, N, F, S"""			"""AML, leukemia"""		Involved in tolerance or repair of DNA crosslinks					2	4	---	---	---	---					
SACS	26278	broad.mit.edu	37	13	23914687	23914687	+	Frame_Shift_Del	DEL	T	T	-			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr13:23914687delT	ENST00000382298.3	-	10	3916	c.3328delA	c.(3328-3330)ttfs	p.I1110fs	SACS_ENST00000382292.3_Frame_Shift_Del_p.I1110fs|SACS_ENST00000402364.1_Frame_Shift_Del_p.I360fs	NM_014363.4	NP_055178.3	Q9NZJ4	SACS_HUMAN	spastic ataxia of Charlevoix-Saguenay (sacsin)	1110					cell death|negative regulation of inclusion body assembly|protein folding	axon|cell body fiber|dendrite|mitochondrion|nucleus	ATP binding|chaperone binding|Hsp70 protein binding|proteasome binding			NS(1)|biliary_tract(1)|breast(3)|central_nervous_system(2)|endometrium(22)|haematopoietic_and_lymphoid_tissue(1)|kidney(15)|large_intestine(54)|lung(49)|ovary(7)|pancreas(1)|prostate(4)|skin(10)|stomach(2)|upper_aerodigestive_tract(6)|urinary_tract(11)	189		all_cancers(29;1.51e-22)|all_epithelial(30;7.82e-19)|all_lung(29;4.71e-18)|Lung SC(185;0.0225)|Breast(139;0.128)		all cancers(112;0.00197)|Epithelial(112;0.00854)|OV - Ovarian serous cystadenocarcinoma(117;0.0298)|Lung(94;0.189)		AAGGCTTCAATTTTTTTTGCC	0.383													7	205	---	---	---	---					
SUGT1P3	0	broad.mit.edu	37	13	41486862	41486862	+	RNA	DEL	A	A	-			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr13:41486862delA	ENST00000304932.4	-	0	214					NR_003365.2																						cgtctctactaaaaaaaaaat	0.517													2	4	---	---	---	---					
NLRC3	197358	broad.mit.edu	37	16	3607531	3607531	+	RNA	DEL	A	A	-			TCGA-E8-A44K-01A-21D-A23U-08	TCGA-E8-A44K-10A-01D-A23U-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ef64fb76-079f-40df-a19c-b375a8f4e4ac	c2bc89b8-c987-4cc1-a5a4-96e21ee64399	g.chr16:3607531delA	ENST00000301749.7	-	0	2505				NLRC3_ENST00000359128.5_RNA|NLRC3_ENST00000603507.1_RNA|NLRC3_ENST00000448023.2_RNA|NLRC3_ENST00000419350.2_RNA	NM_178844.2	NP_849172.2	Q7RTR2	NLRC3_HUMAN	NLR family, CARD domain containing 3						I-kappaB kinase/NF-kappaB cascade|negative regulation of NF-kappaB transcription factor activity|T cell activation	cytoplasm	ATP binding			breast(1)|central_nervous_system(2)|endometrium(1)|kidney(3)|large_intestine(1)|liver(1)|lung(16)|ovary(2)|pancreas(2)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	34						GGGACTTCACAAGATGCCTCA	0.488													4	4	---	---	---	---					
