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	validation_method	t_ref_count	validation_status	validation_tumor_sample	t_alt_count	validation_alt_allele	pox	qox	pox_cutoff	isArtifactMode	oxoGCut
DSG4	147409	broad.mit.edu	37	18	28980927	28980927	+	Missense_Mutation	SNP	A	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr18:28980927A>T	uc002kwr.2	+	9	1496	c.1361A>T	c.(1360-1362)aAg>aTg	p.K454M	DSG4_uc002kwq.2_Missense_Mutation_p.K454M	NM_001134453	NP_001127925	Q86SJ6	DSG4_HUMAN	Homo sapiens desmoglein 4 (DSG4), transcript variant 1, mRNA.	454	Cadherin 4.				homophilic cell adhesion	desmosome|integral to membrane	calcium ion binding			NS(1)|breast(1)|central_nervous_system(6)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(3)|kidney(2)|large_intestine(11)|liver(2)|lung(35)|ovary(4)|skin(1)|stomach(1)|urinary_tract(1)	70			OV - Ovarian serous cystadenocarcinoma(10;0.00504)			GAATTTGATAAGAAGTCAAAA	0.289000														36			29		0	0	0.779181	0	0
PEA15	8682	broad.mit.edu	37	1	160181403	160181403	+	Silent	SNP	C	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr1:160181403C>A	uc001fvl.3	+	3	566	c.132C>A	c.(130-132)ctC>ctA	p.L44L	AK093299_uc001fvj.1_5'Flank|PEA15_uc001fvk.3_Silent_p.L23L	NM_003768	NP_003759	Q15121	PEA15_HUMAN	Homo sapiens phosphoprotein enriched in astrocytes 15 (PEA15), mRNA.	23	DED.				anti-apoptosis|apoptosis|carbohydrate transport|negative regulation of glucose import	cytoplasm|microtubule associated complex	protein binding			large_intestine(1)|lung(4)	5	all_cancers(52;3.11e-18)|all_hematologic(112;0.093)		BRCA - Breast invasive adenocarcinoma(70;0.111)			TAGAACAGCTCAAGTCGGCCT	0.542000														77			13		1.3612e-06	1.42602e-06	0.479597	1	0
AGAP9	642517	broad.mit.edu	37	10	47207813	47207813	+	Splice_Site	SNP	T	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr10:47207813T>C	uc009xnf.2	-	4	508	c.396_splice	c.e4+1	p.H132_splice	AGAP9_uc001jei.3_Splice_Site	NM_001190810	NP_001177739	D3YTF3	D3YTF3_HUMAN	Homo sapiens ArfGAP with GTPase domain, ankyrin repeat and PH domain 9 (AGAP9), mRNA.	132					regulation of ARF GTPase activity		ARF GTPase activator activity|zinc ion binding	p.H228R(20)									TTTACTTACATGGTTTGTACA	0.294000														17			3		0	0	0.115264	0	0
ARHGEF17	9828	broad.mit.edu	37	11	73020470	73020470	+	Missense_Mutation	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr11:73020470G>A	uc001otu.3	+	0	808	c.787G>A	c.(787-789)Gga>Aga	p.G263R	ARHGEF17_uc021qnc.1_Missense_Mutation_p.G263R	NM_014786	NP_055601	Q96PE2	ARHGH_HUMAN	Homo sapiens Rho guanine nucleotide exchange factor (GEF) 17 (ARHGEF17), mRNA.	263					actin cytoskeleton organization|apoptosis|induction of apoptosis by extracellular signals|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction	cytosol	Rho guanyl-nucleotide exchange factor activity			endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(7)|lung(15)|ovary(2)|skin(2)	32						GCAGCTGCCTGGAGCCCAGAG	0.721000														15			19		0	0	0.608945	0	0
C11orf49	79096	broad.mit.edu	37	11	47074069	47074069	+	Splice_Site	SNP	G	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr11:47074069G>T	uc001ndr.3	+	3	386	c.280_splice	c.e3+1	p.D94_splice	C11orf49_uc001nds.3_Splice_Site_p.D94_splice|C11orf49_uc001ndq.3_Splice_Site_p.D94_splice|C11orf49_uc001ndp.3_Splice_Site_p.D94_splice|C11orf49_uc010rgx.2_Splice_Site|C11orf49_uc010rgy.2_Splice_Site_p.D85_splice|C11orf49_uc010rgz.2_Intron	NM_001003677	NP_001003677	Q9H6J7	CK049_HUMAN	Homo sapiens chromosome 11 open reading frame 49 (C11orf49), transcript variant 2, mRNA.	94										central_nervous_system(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(2)|lung(5)|skin(1)	11						CAAAAATGGCGGTAAGTCTTC	0.463000														51			39		7.05121e-23	7.56716e-23	0.853193	1	0
ADAMTS7	11173	broad.mit.edu	37	15	79059041	79059041	+	Missense_Mutation	SNP	T	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr15:79059041T>C	uc002bej.4	-	18	3423	c.3212A>G	c.(3211-3213)aAt>aGt	p.N1071S	ADAMTS7_uc010und.1_3'UTR	NM_014272	NP_055087	Q9UKP4	ATS7_HUMAN	Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif, 7 (ADAMTS7), mRNA.	1071					proteolysis	proteinaceous extracellular matrix	metalloendopeptidase activity|zinc ion binding	p.N1071S(8)|p.N1071N(2)		NS(1)|breast(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(2)|lung(23)|ovary(1)|prostate(8)|skin(9)	54						CTCGTGGAAATTGATGAAATT	0.617000														46			4		0	0	0.150653	0	0
MED17	9440	broad.mit.edu	37	11	93542943	93542943	+	Missense_Mutation	SNP	C	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr11:93542943C>A	uc001pem.4	+	10	1920	c.1645C>A	c.(1645-1647)Ctg>Atg	p.L549M		NM_004268	NP_004259	Q9NVC6	MED17_HUMAN	Homo sapiens mediator complex subunit 17 (MED17), mRNA.	549					androgen receptor signaling pathway|positive regulation of transcription from RNA polymerase II promoter|transcription initiation from RNA polymerase II promoter	mediator complex|transcription factor complex	RNA polymerase II transcription cofactor activity|ligand-dependent nuclear receptor transcription coactivator activity|receptor activity|thyroid hormone receptor binding|vitamin D receptor binding			large_intestine(2)|lung(11)|ovary(1)	14		Acute lymphoblastic leukemia(157;2.31e-05)|all_hematologic(158;0.00824)				CTGGCAAGTACTGAGCTTCAG	0.493000														77			66		2.3441e-25	2.57851e-25	0.870114	1	0
NLRP5	126206	broad.mit.edu	37	19	56511120	56511120	+	Missense_Mutation	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr19:56511120G>A	uc002qmj.3	+	0	29	c.29G>A	c.(28-30)gGa>gAa	p.G10E	NLRP5_uc002qmi.3_Missense_Mutation_p.G10E	NM_153447	NP_703148	P59047	NALP5_HUMAN	Homo sapiens NLR family, pyrin domain containing 5 (NLRP5), mRNA.	10						mitochondrion|nucleolus	ATP binding			breast(1)|central_nervous_system(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(8)|ovary(5)|skin(2)|stomach(4)|upper_aerodigestive_tract(2)	25		Colorectal(82;3.46e-05)|Ovarian(87;0.0481)|Renal(1328;0.157)		GBM - Glioblastoma multiforme(193;0.0326)		cttgaacttggagctgcTGCT	0.517000														160			26		0	0	0.740014	0	0
ZC3H18	124245	broad.mit.edu	37	16	88697571	88697571	+	Missense_Mutation	SNP	C	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr16:88697571C>T	uc010voz.2	+	18	2998	c.2798C>T	c.(2797-2799)gCc>gTc	p.A933V	ZC3H18_uc002fky.3_Missense_Mutation_p.A909V|ZC3H18_uc010chw.3_Non-coding_Transcript|ZC3H18_uc002fkz.3_Missense_Mutation_p.A179V	NM_144604	NP_653205	Q86VM9	ZCH18_HUMAN	Homo sapiens zinc finger CCCH-type containing 18 (ZC3H18), mRNA.	909						nucleus	nucleic acid binding|zinc ion binding			endometrium(5)|haematopoietic_and_lymphoid_tissue(2)|kidney(6)|large_intestine(9)|lung(16)|ovary(1)|skin(2)|upper_aerodigestive_tract(1)	42				BRCA - Breast invasive adenocarcinoma(80;0.0542)		CCCGGCAAAGCCTCGGATCCC	0.642000														101			4		0	0	0.184627	0	0
ZBTB33	10009	broad.mit.edu	37	X	119387346	119387346	+	Missense_Mutation	SNP	C	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chrX:119387346C>T	uc022cdm.1	+	0	76	c.76C>T	c.(76-78)Cgt>Tgt	p.R26C	ZBTB33_uc010nqm.1_Missense_Mutation_p.R26C|ZBTB33_uc004esn.1_Missense_Mutation_p.R26C	NM_006777	NP_006768	Q86T24	KAISO_HUMAN	Homo sapiens zinc finger and BTB domain containing 33 (ZBTB33), transcript variant 2, mRNA.	26	Interaction with NCOR1.|Self-association (By similarity).				Wnt receptor signaling pathway|intracellular signal transduction|regulation of transcription, DNA-dependent|transcription, DNA-dependent	cytoplasm|nucleolus|plasma membrane	DNA binding|protein binding|zinc ion binding			breast(2)|central_nervous_system(2)|endometrium(6)|large_intestine(6)|lung(5)|ovary(2)|pancreas(1)|skin(1)|upper_aerodigestive_tract(1)	26						GAATGAGCAACGTGGCCATGG	0.448000														124			5		0	0	0.217242	0	0
APCDD1	147495	broad.mit.edu	37	18	10487950	10487950	+	Missense_Mutation	SNP	G	A	A	rs112875590		TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr18:10487950G>A	uc002kom.4	+	4	1814	c.1460G>A	c.(1459-1461)cGg>cAg	p.R487Q		NM_153000	NP_694545	Q8J025	APCD1_HUMAN	Homo sapiens adenomatosis polyposis coli down-regulated 1 (APCDD1), mRNA.	487					Wnt receptor signaling pathway|hair follicle development|negative regulation of Wnt receptor signaling pathway	integral to plasma membrane	Wnt-protein binding			NS(1)|breast(1)|endometrium(3)|large_intestine(5)|lung(7)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	22				READ - Rectum adenocarcinoma(15;0.08)		CTGTATGGCCGGGCCCCTGGG	0.592000														87			34		0	0	0.812448	0	0
GALNT11	63917	broad.mit.edu	37	7	151805279	151805279	+	Missense_Mutation	SNP	T	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr7:151805279T>C	uc010lqg.1	+	5	1099	c.869T>C	c.(868-870)gTc>gCc	p.V290A	GALNT11_uc011kvm.1_Missense_Mutation_p.V209A|GALNT11_uc003wku.2_Missense_Mutation_p.V290A|GALNT11_uc011kvn.1_Non-coding_Transcript|GALNT11_uc003wkw.1_Missense_Mutation_p.V38A	NM_022087	NP_071370	Q8NCW6	GLT11_HUMAN	Homo sapiens UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 11 (GalNAc-T11) (GALNT11), mRNA.	290						Golgi membrane|integral to membrane	polypeptide N-acetylgalactosaminyltransferase activity|sugar binding			breast(2)|endometrium(2)|haematopoietic_and_lymphoid_tissue(2)|kidney(2)|large_intestine(5)|lung(7)|prostate(5)|skin(2)	27	all_neural(206;0.187)	all_hematologic(28;0.0592)|Prostate(32;0.214)	OV - Ovarian serous cystadenocarcinoma(82;0.00168)	UCEC - Uterine corpus endometrioid carcinoma (81;0.177)|BRCA - Breast invasive adenocarcinoma(188;0.0932)		TCCCCTGTCGTCCGCGGAGGG	0.602000														35			98		0	0	0.870114	0	0
C15orf42	90381	broad.mit.edu	37	15	90129030	90129030	+	Missense_Mutation	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr15:90129030G>A	uc002boe.3	+	3	1268	c.1268G>A	c.(1267-1269)cGc>cAc	p.R423H	C15orf42_uc021sug.1_Missense_Mutation_p.R422H	NM_152259	NP_689472	Q7Z2Z1	TICRR_HUMAN	Homo sapiens chromosome 15 open reading frame 42 (C15orf42), mRNA.	423					DNA repair|DNA replication|G2/M transition checkpoint|cell cycle|formation of translation preinitiation complex|mitotic cell cycle DNA replication checkpoint|regulation of DNA-dependent DNA replication initiation|response to ionizing radiation	nucleus	chromatin binding|protein binding			NS(1)|central_nervous_system(2)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(10)|lung(21)|ovary(6)|skin(3)|stomach(3)|upper_aerodigestive_tract(2)|urinary_tract(2)	59	Lung NSC(78;0.0237)|all_lung(78;0.0478)		BRCA - Breast invasive adenocarcinoma(143;0.128)			ACTGTGTGCCGCACCAAGGAG	0.542000														57			5		0	0	0.217242	0	0
VPS26B	112936	broad.mit.edu	37	11	134115448	134115448	+	Silent	SNP	C	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr11:134115448C>T	uc001qhe.3	+	5	1431	c.975C>T	c.(973-975)acC>acT	p.T325T		NM_052875	NP_443107	Q4G0F5	VP26B_HUMAN	Homo sapiens vacuolar protein sorting 26 homolog B (S. pombe) (VPS26B), mRNA.	325					protein transport|vacuolar transport	cytosol|retromer complex				breast(1)|endometrium(1)|kidney(1)|large_intestine(4)|lung(7)	14	all_hematologic(175;0.127)	all_cancers(12;1.1e-21)|all_epithelial(12;3.77e-16)|all_lung(97;1.19e-05)|Lung NSC(97;2.76e-05)|Breast(109;0.000182)|Medulloblastoma(222;0.0245)|all_neural(223;0.0505)|Esophageal squamous(93;0.0559)		Epithelial(10;2.43e-10)|all cancers(11;2.94e-09)|BRCA - Breast invasive adenocarcinoma(10;9.57e-09)|OV - Ovarian serous cystadenocarcinoma(99;0.00164)|Lung(977;0.216)		AGGTGCGGACCCCCAGCCAGC	0.652000														14			17		0	0	0.520397	0	0
C9orf174	100499483	broad.mit.edu	37	9	100117239	100117239	+	Missense_Mutation	SNP	A	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr9:100117239A>G	uc011lut.2	+	37	4768	c.3762A>G	c.(3760-3762)atA>atG	p.I1254M	C9orf174_uc004axe.2_Missense_Mutation_p.I1086M|C9orf174_uc011lus.2_Missense_Mutation_p.I904M|C9orf174_uc004axg.2_Missense_Mutation_p.I1115M|C9orf174_uc004axh.2_Non-coding_Transcript	NM_020893	NP_065944	Q9P1Z9	CI174_HUMAN	Homo sapiens chromosome 9 open reading frame 174 (C9orf174), mRNA.	1086						integral to membrane				breast(1)|endometrium(4)|kidney(1)|lung(9)|urinary_tract(1)	16						TTATTTTCATAGAGAAAATCC	0.418000														53			44		0	0	0.859065	0	0
PTGDR	5729	broad.mit.edu	37	14	52734893	52734893	+	Missense_Mutation	SNP	C	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr14:52734893C>A	uc001wzq.3	+	0	463	c.361C>A	c.(361-363)Ctg>Atg	p.L121M		NM_000953	NP_000944	Q13258	PD2R_HUMAN	Homo sapiens prostaglandin D2 receptor (DP) (PTGDR), mRNA.	121						integral to membrane|plasma membrane	prostaglandin D receptor activity|protein binding			breast(1)|central_nervous_system(1)|endometrium(3)|large_intestine(1)|lung(15)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	26	Breast(41;0.0639)|all_epithelial(31;0.0887)				Nedocromil(DB00716)	CTCCTCGACACTGCAACTCCT	0.627000														122			70		1.08321e-29	1.22208e-29	0.870114	1	0
WDR18	57418	broad.mit.edu	37	19	992048	992048	+	Missense_Mutation	SNP	A	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr19:992048A>G	uc002lqm.1	+	7	1051	c.1025A>G	c.(1024-1026)cAc>cGc	p.H342R		NM_024100	NP_077005	Q9BV38	WDR18_HUMAN	Homo sapiens WD repeat domain 18 (WDR18), mRNA.	342										endometrium(1)|kidney(2)|lung(2)|skin(2)	7		Acute lymphoblastic leukemia(61;2.53e-14)|all_hematologic(61;8.18e-10)|Lung NSC(49;1.04e-05)|all_lung(49;1.53e-05)|Breast(49;9.42e-05)|Hepatocellular(1079;0.137)		UCEC - Uterine corpus endometrioid carcinoma (162;6.64e-05)|OV - Ovarian serous cystadenocarcinoma(105;1.09e-113)|Epithelial(107;3.79e-112)|all cancers(105;1.67e-104)|BRCA - Breast invasive adenocarcinoma(158;0.00136)|STAD - Stomach adenocarcinoma(1328;0.18)		TTCAACAAGCACCTGCTGGGC	0.716000														8			14		0	0	0.457914	0	0
PLA2G4F	255189	broad.mit.edu	37	15	42442584	42442584	+	Missense_Mutation	SNP	A	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr15:42442584A>G	uc001zoz.3	-	8	964	c.872T>C	c.(871-873)gTg>gCg	p.V291A	PLA2G4F_uc001zoy.3_5'Flank|PLA2G4F_uc001zpa.3_Missense_Mutation_p.V42A|PLA2G4F_uc010bcr.3_Missense_Mutation_p.V42A|PLA2G4F_uc010bcs.3_Missense_Mutation_p.V78A	NM_213600	NP_998765	Q68DD2	PA24F_HUMAN	Homo sapiens phospholipase A2, group IVF (PLA2G4F), transcript variant 1, mRNA.	291					phospholipid catabolic process	cytosol|lysosomal membrane	metal ion binding|phospholipase A2 activity			breast(1)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(3)|liver(1)|lung(12)|ovary(4)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)	32		all_cancers(109;4.82e-12)|all_epithelial(112;5.64e-11)|Lung NSC(122;2.17e-07)|all_lung(180;8.79e-07)|Melanoma(134;0.091)		GBM - Glioblastoma multiforme(94;8.97e-07)		CCCCAGGGCCACAGAACACTG	0.652000														11			15		0	0	0.457914	0	0
KPNB1	3837	broad.mit.edu	37	17	45727756	45727756	+	Silent	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr17:45727756G>A	uc002ilt.1	+	1	381	c.45G>A	c.(43-45)cgG>cgA	p.R15R	KPNB1_uc010wkw.1_5'Flank	NM_002265	NP_002256	Q14974	IMB1_HUMAN	Homo sapiens karyopherin (importin) beta 1 (KPNB1), mRNA.	15					DNA fragmentation involved in apoptotic nuclear change|NLS-bearing substrate import into nucleus|protein import into nucleus, translocation|ribosomal protein import into nucleus|viral genome transport in host cell|viral infectious cycle	cytosol|nuclear pore|nucleoplasm	nuclear localization sequence binding|protein domain specific binding|zinc ion binding			breast(1)|ovary(1)|pancreas(1)|skin(1)	4						CCCTAGATCGGCTGGAGCTGG	0.716000														32			3		0	0	0.115264	0	0
DOCK4	9732	broad.mit.edu	37	7	111368503	111368503	+	Missense_Mutation	SNP	G	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr7:111368503G>C	uc003vfy.3	-	53	6132	c.5863C>G	c.(5863-5865)Ctg>Gtg	p.L1955V	DOCK4_uc011kml.2_Missense_Mutation_p.L791V|DOCK4_uc011kmm.2_Missense_Mutation_p.L779V|DOCK4_uc003vfw.3_Missense_Mutation_p.L1322V|DOCK4_uc003vfx.3_Missense_Mutation_p.L1910V|DOCK4_uc003vfv.3_Missense_Mutation_p.L223V	NM_014705	NP_055520	Q8N1I0	DOCK4_HUMAN	Homo sapiens dedicator of cytokinesis 4 (DOCK4), mRNA.	1910	Pro-rich.				cell chemotaxis	cytosol|endomembrane system|membrane|stereocilium	GTP binding|PDZ domain binding|Rac GTPase activator activity|Rac GTPase binding|SH3 domain binding|guanyl-nucleotide exchange factor activity|receptor tyrosine kinase binding			NS(1)|breast(1)|central_nervous_system(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(4)|kidney(4)|large_intestine(13)|lung(31)|ovary(2)|skin(2)|stomach(1)|upper_aerodigestive_tract(4)|urinary_tract(4)	72		Acute lymphoblastic leukemia(1;0.0441)				GGGCGCCGCAGAGTCCGCTCG	0.726000														89			5		0	0	0.217242	0	0
VIM	7431	broad.mit.edu	37	10	17276732	17276732	+	Missense_Mutation	SNP	C	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr10:17276732C>G	uc001iou.2	+	5	1336	c.923C>G	c.(922-924)gCc>gGc	p.A308G		NM_003380	NP_003371	P08670	VIME_HUMAN	Homo sapiens vimentin (VIM), mRNA.	308	Coil 2.|Rod.				cellular component disassembly involved in apoptosis|cellular component movement|interspecies interaction between organisms|muscle filament sliding	cytosol|intermediate filament	protein C-terminus binding|structural constituent of cytoskeleton			NS(1)|autonomic_ganglia(1)|breast(1)|endometrium(3)|kidney(1)|large_intestine(4)|liver(2)|lung(18)|ovary(2)|pancreas(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	38						AACAATGACGCCCTGCGCCAG	0.512000														90			15		0	0	0.500413	0	0
FOXE3	2301	broad.mit.edu	37	1	47882415	47882415	+	Missense_Mutation	SNP	A	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr1:47882415A>C	uc001crk.3	+	0	672	c.428A>C	c.(427-429)aAc>aCc	p.N143T		NM_012186	NP_036318	Q13461	FOXE3_HUMAN	Homo sapiens forkhead box E3 (FOXE3), mRNA.	143					cell migration|embryonic organ morphogenesis|enteric nervous system development|hair follicle morphogenesis|hard palate development|lens morphogenesis in camera-type eye|pattern specification process|positive regulation of epithelial cell proliferation|positive regulation of transcription from RNA polymerase II promoter|regulation of sequence-specific DNA binding transcription factor activity|soft palate development|thyroid gland development|thyroid hormone generation	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			lung(3)|prostate(1)|upper_aerodigestive_tract(1)	5				READ - Rectum adenocarcinoma(2;0.0908)		GGCAAGGGCAACTACTGGACG	0.687000														54			26		0	0	0.693898	0	0
MYO7A	4647	broad.mit.edu	37	11	76890090	76890090	+	Splice_Site	SNP	G	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr11:76890090G>T	uc001oyb.2	+	20	2555	c.2283_splice	c.e20-1	p.R761_splice	MYO7A_uc010rsl.2_Splice_Site_p.R761_splice|MYO7A_uc010rsm.1_Splice_Site_p.R750_splice|MYO7A_uc001oyc.2_Splice_Site_p.R761_splice|MYO7A_uc001oyd.3_Splice_Site_p.R101_splice|MYO7A_uc009yus.1_5'Flank|MYO7A_uc009yut.1_5'Flank	NM_000260	NP_000251	Q13402	MYO7A_HUMAN	Homo sapiens myosin VIIA (MYO7A), transcript variant 1, mRNA.	761	IQ 1.				actin filament-based movement|equilibrioception|lysosome organization|sensory perception of sound|visual perception	cytosol|lysosomal membrane|myosin complex|photoreceptor inner segment|photoreceptor outer segment|synapse	ATP binding|actin binding|calmodulin binding|microfilament motor activity			NS(2)|breast(2)|central_nervous_system(1)|endometrium(7)|kidney(1)|large_intestine(10)|lung(32)|ovary(4)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	64						TGCTGTTTCAGGTCTAACTTT	0.587000														7			9		1.12685e-05	1.15306e-05	0.307466	1	0
FGD5	152273	broad.mit.edu	37	3	14862235	14862235	+	Missense_Mutation	SNP	G	A	A	rs61751585		TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr3:14862235G>A	uc003bzc.3	+	0	1767	c.1657G>A	c.(1657-1659)Gtg>Atg	p.V553M	FGD5_uc011avk.2_Missense_Mutation_p.V553M	NM_152536	NP_689749	Q6ZNL6	FGD5_HUMAN	Homo sapiens FYVE, RhoGEF and PH domain containing 5 (FGD5), mRNA.	553					actin cytoskeleton organization|filopodium assembly|regulation of Cdc42 GTPase activity|regulation of cell shape	Golgi apparatus|cytoskeleton|lamellipodium|ruffle	Rho guanyl-nucleotide exchange factor activity|metal ion binding|small GTPase binding			NS(2)|breast(2)|endometrium(3)|kidney(5)|large_intestine(10)|lung(25)|ovary(3)|pancreas(1)|prostate(2)|urinary_tract(1)	54						GTCGTTCTCCGTGGAAGGCCG	0.557000														24			3		0	0	0.115264	0	0
PROM2	150696	broad.mit.edu	37	2	95941238	95941238	+	Missense_Mutation	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr2:95941238G>A	uc002suk.3	+	1	407	c.274G>A	c.(274-276)Gcc>Acc	p.A92T	PROM2_uc002suh.2_Missense_Mutation_p.A92T|PROM2_uc002sui.3_Missense_Mutation_p.A92T|PROM2_uc002suj.3_5'UTR|PROM2_uc002sul.3_5'UTR	NM_001165977	NP_653308	Q8N271	PROM2_HUMAN	Homo sapiens prominin 2 (PROM2), transcript variant 2, mRNA.	92						apical plasma membrane|basolateral plasma membrane|cilium membrane|integral to membrane|microvillus membrane				breast(1)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(8)|lung(12)|ovary(3)|prostate(1)|skin(1)|urinary_tract(1)	32						GAATGAGCTGGCCTCCGTGAA	0.602000														43			23		0	0	0.654019	0	0
DNAJC25	548645	broad.mit.edu	37	9	114429094	114429094	+	Splice_Site	SNP	G	A	A			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr9:114429094G>A	uc004bfn.3	+	2	393	c.337_splice	c.e2-1	p.V113_splice	DNAJC25_uc004bfp.3_Splice_Site_p.V28_splice|DNAJC25_uc011lws.2_Splice_Site_p.V28_splice	NM_004125	NP_004116	Q9H1X3	DJC25_HUMAN	Homo sapiens DNAJC25-GNG10 readthrough (DNAJC25-GNG10), mRNA.	0	J.				protein folding	integral to membrane	heat shock protein binding|unfolded protein binding			kidney(1)|large_intestine(2)|lung(1)|skin(4)	8						CTTTGTTTCAGGTCTCTCAGG	0.522000														23			12		0	0	0.435327	0	0
ATG16L1	55054	broad.mit.edu	37	2	234173559	234173559	+	Silent	SNP	T	C	C			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr2:234173559T>C	uc002vty.3	+	4	668	c.411T>C	c.(409-411)acT>acC	p.T137T	ATG16L1_uc021vyl.1_Silent_p.T21T|ATG16L1_uc002vub.3_Silent_p.T14T|ATG16L1_uc002vtz.3_Intron|ATG16L1_uc002vud.4_Silent_p.T53T|ATG16L1_uc002vua.3_Silent_p.T137T|ATG16L1_uc002vtx.2_Intron	NM_030803	NP_001177196	Q676U5	A16L1_HUMAN	Homo sapiens ATG16 autophagy related 16-like 1 (S. cerevisiae) (ATG16L1), transcript variant 1, mRNA.	137					autophagic vacuole assembly|protein homooligomerization|protein transport	autophagic vacuole|pre-autophagosomal structure membrane	protein binding			breast(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(3)|kidney(2)|large_intestine(5)|lung(7)|prostate(3)|skin(1)	25		Breast(86;0.0013)|Renal(207;0.00339)|all_hematologic(139;0.0116)|all_lung(227;0.0179)|Acute lymphoblastic leukemia(138;0.0327)|Lung NSC(271;0.0539)		Epithelial(121;1.53e-17)|BRCA - Breast invasive adenocarcinoma(100;0.000379)|LUSC - Lung squamous cell carcinoma(224;0.00619)|Lung(119;0.00732)|GBM - Glioblastoma multiforme(43;0.11)		GTTTGCAGACTATCTCTGACC	0.527000														66			36		0	0	0.788014	0	0
MYOM2	9172	broad.mit.edu	37	8	2063780	2063780	+	Missense_Mutation	SNP	C	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr8:2063780C>T	uc003wpx.4	+	25	3347	c.3209C>T	c.(3208-3210)aCt>aTt	p.T1070I	MYOM2_uc011kwi.2_Missense_Mutation_p.T495I	NM_003970	NP_003961	P54296	MYOM2_HUMAN	Homo sapiens myomesin (M-protein) 2, 165kDa (MYOM2), mRNA.	1070					muscle contraction	myosin filament	structural constituent of muscle			autonomic_ganglia(2)|breast(4)|central_nervous_system(3)|endometrium(7)|haematopoietic_and_lymphoid_tissue(11)|kidney(2)|large_intestine(17)|lung(39)|ovary(5)|prostate(1)|skin(10)|upper_aerodigestive_tract(3)	104		Ovarian(12;0.0572)|Colorectal(14;0.0844)|Hepatocellular(245;0.217)		BRCA - Breast invasive adenocarcinoma(11;1.85e-05)|Colorectal(4;0.0101)|READ - Rectum adenocarcinoma(4;0.148)|COAD - Colon adenocarcinoma(4;0.179)		GACAAAGCTACTGGCATTATT	0.383000														39			30		0	0	0.760397	0	0
PTGDR	5729	broad.mit.edu	37	14	52734894	52734894	+	Missense_Mutation	SNP	T	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr14:52734894T>G	uc001wzq.3	+	0	464	c.362T>G	c.(361-363)cTg>cGg	p.L121R		NM_000953	NP_000944	Q13258	PD2R_HUMAN	Homo sapiens prostaglandin D2 receptor (DP) (PTGDR), mRNA.	121						integral to membrane|plasma membrane	prostaglandin D receptor activity|protein binding			breast(1)|central_nervous_system(1)|endometrium(3)|large_intestine(1)|lung(15)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	26	Breast(41;0.0639)|all_epithelial(31;0.0887)				Nedocromil(DB00716)	TCCTCGACACTGCAACTCCTG	0.627000														123			69		0	0	0.870114	0	0
RPAP3	79657	broad.mit.edu	37	12	48080648	48080648	+	Missense_Mutation	SNP	C	T	T			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr12:48080648C>T	uc001rpr.3	-	8	1023	c.907G>A	c.(907-909)Gaa>Aaa	p.E303K	RPAP3_uc010slk.2_Missense_Mutation_p.E144K|RPAP3_uc001rps.3_Missense_Mutation_p.E303K	NM_024604	NP_001139548	Q9H6T3	RPAP3_HUMAN	Homo sapiens RNA polymerase II associated protein 3 (RPAP3), transcript variant 1, mRNA.	303							binding			endometrium(2)|large_intestine(4)|liver(1)|lung(6)|ovary(1)|skin(1)|upper_aerodigestive_tract(1)	16	Lung SC(27;0.192)					GTATAGCATTCAATTGCTCTT	0.353000														30			38		0	0	0.840704	0	0
ARHGAP21	57584	broad.mit.edu	37	10	24885703	24885704	+	Frame_Shift_Ins	INS	-	G	G			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr10:24885703_24885704insG	uc001isb.2	-	16	3929_3930	c.3442_3443insC	c.(3442-3444)cgafs	p.R1148fs	ARHGAP21_uc010qdb.1_Non-coding_Transcript|ARHGAP21_uc009xkl.1_Frame_Shift_Ins_p.R1148fs	NM_020824	NP_065875	Q5T5U3	RHG21_HUMAN	Homo sapiens Rho GTPase activating protein 21 (ARHGAP21), mRNA.	1147	Rho-GAP.				signal transduction	Golgi membrane|cell junction|cytoplasmic vesicle membrane|cytoskeleton	GTPase activator activity|protein binding			NS(1)|breast(4)|central_nervous_system(1)|cervix(1)|endometrium(11)|kidney(4)|large_intestine(17)|lung(21)|ovary(7)|pancreas(1)|prostate(5)|skin(2)|stomach(2)|urinary_tract(1)	78						GTCATCTAGTCGGACGCCGAAA	0.455													---	56	---	---	42	---					
KIAA1704	55425	broad.mit.edu	37	13	45580365	45580367	+	In_Frame_Del	DEL	GAT	-	-	rs138421508		TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr13:45580365_45580367delGAT	uc001uzq.3	+	2	353_355	c.250_252delGAT	c.(250-252)gatdel	p.D88del	KIAA1704_uc010tfo.1_Non-coding_Transcript|KIAA1704_uc001uzr.1_In_Frame_Del_p.D88del|KIAA1704_uc001uzs.3_5'UTR|KIAA1704_uc001uzt.3_5'UTR	NM_018559	NP_061029	Q8IXQ4	K1704_HUMAN	Homo sapiens KIAA1704 (KIAA1704), mRNA.	88	Poly-Asp.									breast(1)|endometrium(1)|kidney(2)|large_intestine(3)|lung(1)|pancreas(1)|prostate(2)|skin(1)	12		Lung NSC(96;0.00143)|Prostate(109;0.0137)|Breast(139;0.0192)|Lung SC(185;0.0367)|Hepatocellular(98;0.133)	KIRC - Kidney renal clear cell carcinoma(16;0.234)	GBM - Glioblastoma multiforme(144;0.000313)|BRCA - Breast invasive adenocarcinoma(63;0.126)		Ggatgatgacgatgatgatgatg	0.335													---	207	---	---	7	---					
DQ586822	0	broad.mit.edu	37	15	84946555	84946556	+	RNA	INS	-	TT	TT	rs71453238		TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr15:84946555_84946556insTT	uc002bke.2	-	0		c.694_695insAA								Homo sapiens cDNA FLJ34196 fis, clone FCBBF3019437.																		CGAAGGGAGGAttttttttttt	0.515													---	3	---	---	4	---					
PVRL2	5819	broad.mit.edu	37	19	45349842	45349844	+	In_Frame_Del	DEL	GCT	-	-			TCGA-DW-7842-01A-11D-2136-08	TCGA-DW-7842-10A-01D-2136-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	fe91ee01-61e4-4310-b1e9-387033d215a6	bbdb56a6-a63a-419c-91dc-54bd9502aa64	g.chr19:45349842_45349844delGCT	uc002ozw.1	+	0	450_452	c.60_62delGCT	c.(58-63)ccgctg>ccg	p.L27del	PVRL2_uc002ozv.3_In_Frame_Del_p.L27del	NM_001042724	NP_001036189	Q92692	PVRL2_HUMAN	Homo sapiens poliovirus receptor-related 2 (herpesvirus entry mediator B) (PVRL2), transcript variant delta, mRNA.	27					adherens junction organization|adhesion to symbiont|cell junction assembly|homophilic cell adhesion|positive regulation of immunoglobulin mediated immune response|positive regulation of mast cell activation|positive regulation of natural killer cell mediated cytotoxicity directed against tumor cell target|susceptibility to T cell mediated cytotoxicity|susceptibility to natural killer cell mediated cytotoxicity|viral envelope fusion with host membrane|virion attachment, binding of host cell surface coreceptor	cell surface|integral to membrane|zonula adherens	cell adhesion molecule binding|coreceptor activity|protein homodimerization activity			breast(1)|endometrium(1)|large_intestine(6)|lung(5)	13	Lung NSC(12;0.00195)|all_lung(12;0.00522)	Ovarian(192;0.0728)|all_neural(266;0.112)		OV - Ovarian serous cystadenocarcinoma(262;0.0143)		tgctgtggccgctgctgctgctg	0.759													---	3	---	---	3	---					
