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
COL27A1	85301	broad.mit.edu	37	9	116931244	116931244	+	Missense_Mutation	SNP	A	A	C			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr9:116931244A>C	uc011lxl.2	+	2	1409	c.1409A>C	c.(1408-1410)aAg>aCg	p.K470T	COL27A1_uc004bii.3_Non-coding_Transcript|COL27A1_uc010mvd.2_Missense_Mutation_p.K320T	NM_032888	NP_116277	Q8IZC6	CORA1_HUMAN	Homo sapiens collagen, type XXVII, alpha 1 (COL27A1), mRNA.	470	Pro-rich.				cell adhesion		extracellular matrix structural constituent			central_nervous_system(2)|endometrium(6)|haematopoietic_and_lymphoid_tissue(3)|kidney(4)|large_intestine(17)|lung(30)|ovary(4)|prostate(6)|skin(3)|soft_tissue(1)|stomach(1)|urinary_tract(3)	80						CATGCCAGTAAGCCGGCCTCT	0.592000													102	150					0	0	1	0	0
WDFY2	115825	broad.mit.edu	37	13	52301855	52301855	+	Missense_Mutation	SNP	C	C	T			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr13:52301855C>T	uc001vfp.3	+	5	867	c.527C>T	c.(526-528)tCa>tTa	p.S176L	WDFY2_uc010ads.1_Missense_Mutation_p.S176L|WDFY2_uc010adt.1_Non-coding_Transcript	NM_052950	NP_443182	Q96P53	WDFY2_HUMAN	Homo sapiens WD repeat and FYVE domain containing 2 (WDFY2), mRNA.	176							metal ion binding			breast(1)|endometrium(5)|kidney(1)|large_intestine(2)|lung(4)|skin(2)|upper_aerodigestive_tract(1)	16		Breast(56;0.000208)|Lung NSC(96;0.000517)|Prostate(109;0.0041)|Hepatocellular(98;0.0652)|Myeloproliferative disorder(33;0.164)|all_neural(104;0.191)		GBM - Glioblastoma multiforme(99;9e-08)		GGTGACCACTCAGGCCAAGTA	0.403000													10	74					0	0	1	0	0
DZIP3	9666	broad.mit.edu	37	3	108391411	108391411	+	Missense_Mutation	SNP	C	C	A			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr3:108391411C>A	uc003dxd.3	+	22	2919	c.2497C>A	c.(2497-2499)Cag>Aag	p.Q833K	DZIP3_uc003dxf.1_Missense_Mutation_p.Q833K|DZIP3_uc011bhm.2_Missense_Mutation_p.Q284K	NM_014648	NP_055463	Q86Y13	DZIP3_HUMAN	Homo sapiens DAZ interacting protein 3, zinc finger (DZIP3), mRNA.	833					protein polyubiquitination	cytoplasm	RNA binding|polyubiquitin binding|ubiquitin-protein ligase activity|zinc ion binding			breast(3)|central_nervous_system(1)|endometrium(3)|large_intestine(9)|lung(21)|ovary(1)|pancreas(1)|prostate(5)|skin(1)	45						TTTCAGATCTCAGTGGGAAAT	0.363000													4	32					0	0	1	0	0
SLC7A6	9057	broad.mit.edu	37	16	68309107	68309107	+	Missense_Mutation	SNP	G	G	C			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr16:68309107G>C	uc002evt.2	+	3	791	c.478G>C	c.(478-480)Gat>Cat	p.D160H	SLC7A6_uc010cfb.2_Non-coding_Transcript|SLC7A6_uc002evv.2_Non-coding_Transcript|SLC7A6_uc002evu.2_Missense_Mutation_p.D160H|SLC7A6_uc010cfc.1_Non-coding_Transcript	NM_001076785	NP_003974	Q92536	YLAT2_HUMAN	Homo sapiens solute carrier family 7 (amino acid transporter light chain, y+L system), member 6 (SLC7A6), transcript variant 1, mRNA.	160					blood coagulation|cellular amino acid metabolic process|ion transport|leukocyte migration|protein complex assembly	basolateral plasma membrane|integral to plasma membrane	amino acid transmembrane transporter activity|antiporter activity			breast(1)|central_nervous_system(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(3)|lung(4)|prostate(1)|skin(1)	16		Ovarian(137;0.0563)		OV - Ovarian serous cystadenocarcinoma(108;0.034)|Epithelial(162;0.0948)		CCCCAGCTGTGATCCCCCATA	0.582000													8	177					0	0	1	0	0
PPP2R3B	28227	broad.mit.edu	37	X	347131	347131	+	Missense_Mutation	SNP	C	C	T			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chrX:347131C>T	uc004cpg.3	-	0	560	c.296G>A	c.(295-297)gGc>gAc	p.G99D	PPP2R3B_uc011mha.2_5'UTR	NM_013239	NP_037371	Q9Y5P8	P2R3B_HUMAN	Homo sapiens protein phosphatase 2, regulatory subunit B'', beta (PPP2R3B), mRNA.	99					cell cycle arrest|protein dephosphorylation	nucleus|protein phosphatase type 2A complex	calcium ion binding|protein phosphatase type 2A regulator activity|protein serine/threonine phosphatase activity			endometrium(5)|lung(5)|skin(1)	11		all_cancers(21;4.28e-07)|all_epithelial(21;2.07e-08)|all_lung(23;2.81e-05)|Lung NSC(23;0.000693)|Lung SC(21;0.122)				TCTACGGGTGCCTCGAACGTG	0.701000													6	65					0	0	1	0	0
TMEM132B	114795	broad.mit.edu	37	12	126138656	126138656	+	Silent	SNP	G	G	A			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr12:126138656G>A	uc001uhe.1	+	8	2645	c.2637G>A	c.(2635-2637)ccG>ccA	p.P879P	TMEM132B_uc001uhf.1_Silent_p.P391P	NM_052907	NP_443139	Q14DG7	T132B_HUMAN	Homo sapiens transmembrane protein 132B (TMEM132B), mRNA.	879						integral to membrane		p.P879L(1)		NS(1)|breast(9)|central_nervous_system(1)|cervix(1)|endometrium(7)|kidney(2)|large_intestine(11)|liver(1)|lung(45)|ovary(5)|pancreas(1)|prostate(4)|skin(15)|upper_aerodigestive_tract(3)|urinary_tract(1)	107	all_neural(191;0.101)|Medulloblastoma(191;0.163)			OV - Ovarian serous cystadenocarcinoma(86;0.000423)|Epithelial(86;0.00394)|all cancers(50;0.0362)		GGAAGTCACCGGACCCCAATA	0.517000													25	26					0	0	1	0	0
ZNF835	90485	broad.mit.edu	37	19	57176120	57176120	+	Silent	SNP	C	C	T			TCGA-EM-A3FQ-06A-11D-A21A-08	TCGA-EM-A3FQ-10A-01D-A21A-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	31ea2466-3e87-4ec2-a15c-0722473852e7	2125f0b1-c6b9-4b65-a6db-9fd4422e7c7e	g.chr19:57176120C>T	uc010ygn.2	-	1	674	c.447G>A	c.(445-447)caG>caA	p.Q149Q		NM_001005850	NP_001005850			Homo sapiens zinc finger protein 835 (ZNF835), mRNA.											endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(10)|lung(22)|pancreas(3)|prostate(3)|skin(1)|stomach(1)|upper_aerodigestive_tract(3)	47						GGTGCACGCTCTGGCTGAAGG	0.637000													7	65					0	0	1	0	0