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
WAPAL	23063	broad.mit.edu	37	10	88277723	88277723	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr10:88277723C>A	uc001kdn.3	-	2	242	c.233G>T	c.(232-234)tGg>tTg	p.W78L	WAPAL_uc001kdo.3_Missense_Mutation_p.W35L|WAPAL_uc009xsw.3_Missense_Mutation_p.W35L|WAPAL_uc010qmh.1_Missense_Mutation_p.W35L|WAPAL_uc010qmi.1_Missense_Mutation_p.W72L|WAPAL_uc010qmj.1_Missense_Mutation_p.W35L	NM_015045	NP_055860	Q7Z5K2	WAPL_HUMAN	Homo sapiens wings apart-like homolog (Drosophila) (WAPAL), mRNA.	35	Mediates interaction with the cohesin complex.				cell division|interspecies interaction between organisms|mitosis|negative regulation of DNA replication|negative regulation of chromatin binding|negative regulation of sister chromatid cohesion|protein localization to chromatin|regulation of cohesin localization to chromatin	chromatin|cohesin complex|cytoplasm	protein binding			breast(2)|endometrium(2)|kidney(5)|large_intestine(6)|lung(13)|ovary(2)|stomach(1)	31						GGTCTCTCCCCATTTTGTGCT	0.403000													4	77					0	0	1	0	0
TNFRSF13B	23495	broad.mit.edu	37	17	16843703	16843703	+	Missense_Mutation	SNP	C	C	A	rs150101848	byFrequency	TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr17:16843703C>A	uc002gqs.1	-	3	581	c.568G>T	c.(568-570)Ggg>Tgg	p.G190W	TNFRSF13B_uc010vwt.1_Non-coding_Transcript|TNFRSF13B_uc002gqt.1_Missense_Mutation_p.G144W	NM_012452	NP_036584	O14836	TR13B_HUMAN	Homo sapiens tumor necrosis factor receptor superfamily, member 13B (TNFRSF13B), mRNA.	190					cell surface receptor linked signaling pathway	integral to plasma membrane	protein binding|receptor activity			endometrium(1)|kidney(2)|large_intestine(4)|liver(1)|lung(7)|skin(1)	16						CAGGGATCCCCCCTCTTCTTG	0.647000									IgA Deficiency, Selective				4	97					0	0	1	0	0
SLC39A2	29986	broad.mit.edu	37	14	21469223	21469223	+	Missense_Mutation	SNP	G	G	A	rs144375696	byFrequency	TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr14:21469223G>A	uc001vyr.3	+	3	607	c.415G>A	c.(415-417)Gaa>Aaa	p.E139K	SLC39A2_uc001vys.3_Missense_Mutation_p.E40K	NM_014579	NP_055394	Q9NP94	S39A2_HUMAN	Homo sapiens solute carrier family 39 (zinc transporter), member 2 (SLC39A2), transcript variant 1, mRNA.	139						cytoplasmic membrane-bounded vesicle|integral to plasma membrane	zinc ion transmembrane transporter activity			breast(2)|central_nervous_system(1)|large_intestine(4)|lung(4)|ovary(2)|upper_aerodigestive_tract(1)	14	all_cancers(95;0.00267)		OV - Ovarian serous cystadenocarcinoma(11;1.34e-10)|Epithelial(56;1.57e-08)|all cancers(55;7.45e-08)	GBM - Glioblastoma multiforme(265;0.0187)		AGTGCAGGACGAAGAATGGGG	0.547000													32	164					0	0	1	0	0
TMEM217	221468	broad.mit.edu	37	6	37186257	37186257	+	Missense_Mutation	SNP	T	T	C			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr6:37186257T>C	uc003onl.3	-	1	631	c.550A>G	c.(550-552)Att>Gtt	p.I184V	TMEM217_uc010jwr.3_Missense_Mutation_p.I184V|TMEM217_uc010jws.3_Intron|TMEM217_uc003onm.4_Missense_Mutation_p.I184V	NM_145316	NP_660359	Q8N7C4	TM217_HUMAN	Homo sapiens transmembrane protein 217 (TMEM217), transcript variant 1, mRNA.	184						integral to membrane				endometrium(2)|kidney(1)|large_intestine(5)|lung(1)	9						ccACTCGAAATTGATAATCTT	0.478000													4	113					0	0	1	0	0
PTGFR	5737	broad.mit.edu	37	1	79002163	79002163	+	Silent	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:79002163C>A	uc001din.3	+	2	1137	c.871C>A	c.(871-873)Cga>Aga	p.R291R	PTGFR_uc001dim.3_3'UTR	NM_000959	NP_000950	P43088	PF2R_HUMAN	Homo sapiens prostaglandin F receptor (FP) (PTGFR), transcript variant 1, mRNA.	291					parturition	extracellular region|integral to plasma membrane	prostaglandin F receptor activity	p.R291R(1)|p.R290M(1)		breast(6)|endometrium(2)|kidney(1)|large_intestine(6)|lung(11)|ovary(3)|prostate(1)|skin(2)|urinary_tract(1)	33				Colorectal(170;0.248)	Bimatoprost(DB00905)|Latanoprost(DB00654)|Travoprost(DB00287)	TTTTGCTCTCCGAATGGCAAC	0.388000													4	115					0	0	1	0	0
ENPP2	5168	broad.mit.edu	37	8	120575111	120575111	+	Nonsense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr8:120575111C>A	uc003yos.2	-	24	2649	c.2563G>T	c.(2563-2565)Gag>Tag	p.E855*	ENPP2_uc011lic.2_Nonsense_Mutation_p.E341*|ENPP2_uc003yor.2_Nonsense_Mutation_p.E438*|ENPP2_uc010mdd.2_Nonsense_Mutation_p.E828*|ENPP2_uc003yot.2_Nonsense_Mutation_p.E803*	NM_006209	NP_006200	Q13822	ENPP2_HUMAN	Homo sapiens ectonucleotide pyrophosphatase/phosphodiesterase 2 (ENPP2), transcript variant 1, mRNA.	803					G-protein coupled receptor protein signaling pathway|cellular component movement|chemotaxis|immune response|phosphate metabolic process|phosphatidylcholine catabolic process|regulation of cell migration	extracellular space|integral to plasma membrane	alkylglycerophosphoethanolamine phosphodiesterase activity|calcium ion binding|lysophospholipase activity|nucleic acid binding|nucleotide diphosphatase activity|phosphodiesterase I activity|polysaccharide binding|scavenger receptor activity|transcription factor binding|zinc ion binding	p.N854N(1)		breast(1)|central_nervous_system(3)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(15)|lung(30)|ovary(2)|prostate(2)|skin(4)|upper_aerodigestive_tract(4)	69	Lung NSC(37;5.03e-06)|Ovarian(258;0.0249)|Hepatocellular(40;0.161)		STAD - Stomach adenocarcinoma(47;0.00185)			CAGCTCTCCTCGTTGTCAGGC	0.483000													5	79					0	0	1	0	0
HAPLN1	1404	broad.mit.edu	37	5	82940276	82940276	+	Silent	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr5:82940276C>A	uc003kim.3	-	2	752	c.681G>T	c.(679-681)ggG>ggT	p.G227G	HAPLN1_uc003kin.3_Silent_p.G227G	NM_001884	NP_001875	P10915	HPLN1_HUMAN	Homo sapiens hyaluronan and proteoglycan link protein 1 (HAPLN1), mRNA.	227	Link 1.				cell adhesion	proteinaceous extracellular matrix	hyaluronic acid binding			breast(1)|endometrium(1)|kidney(1)|large_intestine(12)|liver(1)|lung(15)|ovary(1)|prostate(1)|skin(1)	34		Lung NSC(167;0.0484)|all_lung(232;0.0522)|Ovarian(174;0.142)		OV - Ovarian serous cystadenocarcinoma(54;7.82e-42)|Epithelial(54;5.88e-35)|all cancers(79;1.14e-29)		TGTTCTGCCCCCCACAGGGCT	0.517000													19	87					0	0	1	0	0
GTF3C2	2976	broad.mit.edu	37	2	27564920	27564920	+	Silent	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr2:27564920G>T	uc002rju.1	-	3	1180	c.783C>A	c.(781-783)ctC>ctA	p.L261L	GTF3C2_uc002rjv.1_Silent_p.L250L|GTF3C2_uc002rjw.1_Silent_p.L250L|GTF3C2_uc010eyz.2_Silent_p.L250L	NM_001521	NP_001512	Q8WUA4	TF3C2_HUMAN	Homo sapiens general transcription factor IIIC, polypeptide 2, beta 110kDa (GTF3C2), transcript variant 1, mRNA.	250						transcription factor TFIIIC complex				central_nervous_system(4)|endometrium(6)|kidney(1)|large_intestine(9)|lung(10)|ovary(1)|pancreas(1)|prostate(2)|skin(2)|urinary_tract(2)	38	Acute lymphoblastic leukemia(172;0.155)|all_hematologic(175;0.215)					CCTCAACCTGGAGAAAAAAGT	0.562000													5	95					0	0	1	0	0
STRN4	29888	broad.mit.edu	37	19	47236332	47236332	+	Nonsense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr19:47236332G>T	uc002pfm.3	-	4	734	c.701C>A	c.(700-702)tCg>tAg	p.S234*	STRN4_uc002pfl.3_Nonsense_Mutation_p.S234*|STRN4_uc010xyf.2_Non-coding_Transcript|STRN4_uc010xyg.1_Non-coding_Transcript	NM_001039877	NP_001034966	Q9NRL3	STRN4_HUMAN	Homo sapiens striatin, calmodulin binding protein 4 (STRN4), transcript variant 2, mRNA.	234						cytoplasm|membrane	armadillo repeat domain binding|calmodulin binding|protein complex binding|protein phosphatase 2A binding			NS(1)|endometrium(3)|kidney(2)|large_intestine(4)|lung(4)|prostate(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	17		Ovarian(192;0.0129)|all_neural(266;0.0459)|Breast(70;0.212)		OV - Ovarian serous cystadenocarcinoma(262;0.000563)|all cancers(93;0.00138)|Epithelial(262;0.0217)|GBM - Glioblastoma multiforme(486;0.035)		CACCAGCAGCGACTCCCCACC	0.647000													6	36					0	0	1	0	0
ALG12	79087	broad.mit.edu	37	22	50297538	50297538	+	Missense_Mutation	SNP	A	A	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr22:50297538A>G	uc003biy.3	-	9	1689	c.1415T>C	c.(1414-1416)gTc>gCc	p.V472A		NM_024105	NP_077010	Q9BV10	ALG12_HUMAN	Homo sapiens asparagine-linked glycosylation 12, alpha-1,6-mannosyltransferase homolog (S. cerevisiae) (ALG12), mRNA.	472					GPI anchor biosynthetic process|dolichol-linked oligosaccharide biosynthetic process|post-translational protein modification|protein N-linked glycosylation via asparagine|protein folding	integral to membrane|intrinsic to endoplasmic reticulum membrane				endometrium(1)|kidney(1)|large_intestine(2)|lung(5)|prostate(3)	12		all_cancers(38;8.58e-10)|all_epithelial(38;1.15e-08)|all_lung(38;0.000109)|Lung NSC(38;0.0018)|Breast(42;0.00191)|Ovarian(80;0.0164)|Lung SC(80;0.164)		BRCA - Breast invasive adenocarcinoma(115;0.199)|LUAD - Lung adenocarcinoma(64;0.247)		CTGCAGGTGGACGTTGAAGGG	0.657000													3	114					0	0	1	0	0
CNNM1	26507	broad.mit.edu	37	10	101147923	101147923	+	Missense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr10:101147923G>T	uc010qpi.2	+	9	2891	c.2602G>T	c.(2602-2604)Ggg>Tgg	p.G868W	CNNM1_uc001kpp.4_Missense_Mutation_p.G847W|CNNM1_uc009xwf.3_Intron|CNNM1_uc009xwg.3_Missense_Mutation_p.G247W	NM_020348	NP_065081	Q9NRU3	CNNM1_HUMAN	Homo sapiens cyclin M1 (CNNM1), mRNA.	847					ion transport	integral to membrane|plasma membrane				NS(1)|breast(2)|endometrium(3)|kidney(1)|large_intestine(10)|lung(5)|ovary(1)|prostate(1)|skin(1)	25		Colorectal(252;0.234)		Epithelial(162;6.82e-10)|all cancers(201;5.62e-08)		CCGCTCAGACGGGCTGAGAAG	0.597000													4	94					0	0	1	0	0
GGT5	2687	broad.mit.edu	37	22	24621350	24621350	+	Nonsense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr22:24621350C>A	uc002zzp.4	-	9	1786	c.1369G>T	c.(1369-1371)Gga>Tga	p.G457*	GGT5_uc002zzo.4_Nonsense_Mutation_p.G456*|GGT5_uc002zzr.4_Nonsense_Mutation_p.G424*|GGT5_uc002zzq.4_Nonsense_Mutation_p.G424*|GGT5_uc011ajm.2_Nonsense_Mutation_p.G380*	NM_001099781	NP_001093251	P36269	GGT5_HUMAN	Homo sapiens gamma-glutamyltransferase 5 (GGT5), transcript variant 1, mRNA.	456					glutathione biosynthetic process|hormone biosynthetic process|leukotriene biosynthetic process|prostanoid metabolic process	integral to membrane|plasma membrane	acyltransferase activity|gamma-glutamyltransferase activity			breast(1)|endometrium(2)|kidney(2)|large_intestine(4)|lung(11)|ovary(2)|prostate(3)|skin(3)	28						CAGCACCTTCCGGGAGCTCCA	0.617000													4	106					0	0	1	0	0
TNN	63923	broad.mit.edu	37	1	175054615	175054615	+	Silent	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:175054615C>T	uc001gkl.1	+	5	1422	c.1309C>T	c.(1309-1311)Ctg>Ttg	p.L437L	TNN_uc010pmx.1_Silent_p.L437L	NM_022093	NP_071376	Q9UQP3	TENN_HUMAN	Homo sapiens tenascin N (TNN), mRNA.	437	Fibronectin type-III 2.				cell growth|cell migration|signal transduction	extracellular space|proteinaceous extracellular matrix				NS(1)|central_nervous_system(2)|cervix(1)|endometrium(13)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(29)|liver(1)|lung(81)|ovary(5)|prostate(6)|skin(5)|stomach(4)|upper_aerodigestive_tract(3)|urinary_tract(3)	156		Breast(1374;0.000962)		KIRC - Kidney renal clear cell carcinoma(1967;0.00198)		GCCGATCCTCCTGAATGGCAG	0.517000													6	12					0	0	1	0	0
CTDSPL2	51496	broad.mit.edu	37	15	44788656	44788656	+	Splice_Site	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr15:44788656C>A	uc001ztr.3	+	6	1186	c.770_splice	c.e6+1	p.P257_splice	CTDSPL2_uc001zts.3_Splice_Site_p.P257_splice|CTDSPL2_uc001ztt.3_Splice_Site_p.P257_splice|CTDSPL2_uc010bdv.3_Splice_Site_p.P185_splice	NM_016396	NP_057480	Q05D32	CTSL2_HUMAN	Homo sapiens CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 (CTDSPL2), mRNA.	257							phosphoprotein phosphatase activity			breast(1)|endometrium(1)|kidney(2)|large_intestine(3)|lung(4)|upper_aerodigestive_tract(2)	13		all_cancers(109;4.36e-14)|all_epithelial(112;9.8e-12)|Lung NSC(122;1.66e-07)|all_lung(180;1.47e-06)|Melanoma(134;0.0122)		all cancers(107;1.02e-20)|GBM - Glioblastoma multiforme(94;1.49e-06)|COAD - Colon adenocarcinoma(120;0.0857)|Colorectal(105;0.0905)		GTATTTGACCCGTGAGTTGCT	0.393000													3	36					0	0	1	0	0
SLC2A9	56606	broad.mit.edu	37	4	9982359	9982359	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:9982359C>T	uc003gmc.3	-	4	599	c.538G>A	c.(538-540)Gtc>Atc	p.V180I	SLC2A9_uc003gmd.3_Missense_Mutation_p.V151I	NM_020041	NP_064425	Q9NRM0	GTR9_HUMAN	Homo sapiens solute carrier family 2 (facilitated glucose transporter), member 9 (SLC2A9), transcript variant 1, mRNA.	180					glucose transport|urate metabolic process	integral to membrane|plasma membrane	sugar:hydrogen symporter activity	p.I180M(1)		NS(1)|breast(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(5)|lung(12)|ovary(3)|pancreas(1)|prostate(2)|skin(4)|stomach(1)	35						CTGAGGGCGACGCCTGTAGAG	0.557000													4	43					0	0	1	0	0
PREP	5550	broad.mit.edu	37	6	105821366	105821366	+	Missense_Mutation	SNP	A	A	C			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr6:105821366A>C	uc003prc.3	-	4	706	c.473T>G	c.(472-474)gTt>gGt	p.V158G		NM_002726	NP_002717	P48147	PPCE_HUMAN	Homo sapiens prolyl endopeptidase (PREP), mRNA.	158					proteolysis		serine-type endopeptidase activity			breast(1)|endometrium(2)|large_intestine(7)|lung(12)|ovary(3)|skin(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	29		all_cancers(87;0.000128)|Acute lymphoblastic leukemia(125;1.9e-08)|all_hematologic(75;9.25e-07)|all_epithelial(87;0.0344)|Lung NSC(302;0.191)|Colorectal(196;0.202)			Oxytocin(DB00107)	GGCACCATCAACTTTCATGAA	0.473000													10	83					0	0	1	0	0
CLASP2	23122	broad.mit.edu	37	3	33552113	33552113	+	Missense_Mutation	SNP	T	T	C			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr3:33552113T>C	uc021wvc.1	-	36	4489	c.4278A>G	c.(4276-4278)atA>atG	p.I1426M	CLASP2_uc003cfs.3_Missense_Mutation_p.I625M|CLASP2_uc021wva.1_Missense_Mutation_p.I500M|CLASP2_uc021wvb.1_Missense_Mutation_p.I1205M	NM_015097	NP_055912	B2RTR1	B2RTR1_HUMAN	Homo sapiens cytoplasmic linker associated protein 2 (CLASP2), transcript variant 1, mRNA.	1427										breast(2)|central_nervous_system(2)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(7)|lung(19)|ovary(3)|prostate(1)|stomach(1)|upper_aerodigestive_tract(1)	48						ACACTCTCTCTATCACTTTTG	0.413000													9	61					0	0	1	0	0
LINC00336	401253	broad.mit.edu	37	6	33561062	33561062	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr6:33561062C>T	uc003oew.1	-	0	54	c.52G>A	c.(52-54)Ggc>Agc	p.G18S						Homo sapiens long intergenic non-protein coding RNA 336 (LINC00336), non-coding RNA.																		CCACGACTGCCAGGCCACCCC	0.687000													7	15					0	0	1	0	0
MYRIP	25924	broad.mit.edu	37	3	40211572	40211572	+	Silent	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr3:40211572C>A	uc003cka.3	+	7	996	c.861C>A	c.(859-861)ccC>ccA	p.P287P	MYRIP_uc010hhu.3_Non-coding_Transcript|MYRIP_uc010hhv.3_Silent_p.P287P|MYRIP_uc010hhw.3_Silent_p.P198P|MYRIP_uc011ayz.2_Silent_p.P100P	NM_015460	NP_056275	Q8NFW9	MYRIP_HUMAN	Homo sapiens myosin VIIA and Rab interacting protein (MYRIP), mRNA.	287	Myosin-binding.				intracellular protein transport		actin binding|zinc ion binding			breast(1)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(9)|liver(2)|lung(10)|ovary(2)|skin(3)|stomach(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	34				KIRC - Kidney renal clear cell carcinoma(284;0.174)|Kidney(284;0.206)		ACCGTGCTCCCGCTGCCCTCT	0.597000													4	88					0	0	1	0	0
CLCN3	1182	broad.mit.edu	37	4	170625197	170625197	+	Missense_Mutation	SNP	G	G	C			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:170625197G>C	uc003ish.3	+	9	2171	c.1612G>C	c.(1612-1614)Gga>Cga	p.G538R	CLCN3_uc003isi.3_Missense_Mutation_p.G538R|CLCN3_uc011cka.2_Missense_Mutation_p.G511R|CLCN3_uc011cjz.2_Missense_Mutation_p.G521R|CLCN3_uc003isj.2_Missense_Mutation_p.G511R	NM_173872	NP_776297	P51790	CLCN3_HUMAN	Homo sapiens chloride channel 3 (CLCN3), transcript variant e, mRNA.	538					endosomal lumen acidification	Golgi membrane|cell surface|early endosome membrane|integral to membrane|late endosome membrane|transport vesicle membrane	ATP binding|PDZ domain binding|antiporter activity|protein heterodimerization activity|protein homodimerization activity|voltage-gated chloride channel activity			breast(5)|endometrium(3)|large_intestine(8)|lung(8)|ovary(1)|skin(1)|stomach(2)|upper_aerodigestive_tract(1)	29		Prostate(90;0.00601)|Renal(120;0.0183)		GBM - Glioblastoma multiforme(119;0.0233)|LUSC - Lung squamous cell carcinoma(193;0.131)		AGCGATCGCAGGAAGGATTGT	0.507000													13	70					0	0	1	0	0
FCGR2C	9103	broad.mit.edu	37	1	161561139	161561139	+	RNA	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:161561139C>T	uc009wuj.2	+	4		c.834C>T			FCGR2C_uc009wuk.2_Non-coding_Transcript|FCGR2C_uc021pdh.1_Non-coding_Transcript|FCGR2C_uc021pdi.1_Non-coding_Transcript|FCGR2C_uc021pdj.1_Non-coding_Transcript					Homo sapiens Fc fragment of IgG, low affinity IIc, receptor for (CD32) (gene/pseudogene) (FCGR2C), mRNA.											lung(2)	2	all_cancers(52;4.89e-16)|all_hematologic(112;0.0207)		BRCA - Breast invasive adenocarcinoma(70;0.00376)			GCACAGGAAACATAGGCTACA	0.498000													7	55					0	0	1	0	0
PAX4	5078	broad.mit.edu	37	7	127255106	127255106	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr7:127255106C>T	uc010lld.1	-	1	370	c.164G>A	c.(163-165)cGc>cAc	p.R55H	PAX4_uc003vmf.2_Missense_Mutation_p.R53H|PAX4_uc003vmg.1_Missense_Mutation_p.R55H|PAX4_uc003vmh.3_Missense_Mutation_p.R53H	NM_006193	NP_006184	O43316	PAX4_HUMAN	Homo sapiens paired box 4 (PAX4), mRNA.	63	Paired.				cell differentiation|endocrine pancreas development|organ morphogenesis	nucleus	sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity			cervix(1)|kidney(2)|large_intestine(6)|lung(20)|ovary(1)|prostate(1)|skin(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	35						GACACCTGTGCGGTAGTAACG	0.572000													27	114					0	0	1	0	0
PKHD1	5314	broad.mit.edu	37	6	51613252	51613252	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr6:51613252C>A	uc003pah.1	-	57	9438	c.9162G>T	c.(9160-9162)gaG>gaT	p.E3054D	PKHD1_uc010jzn.1_Missense_Mutation_p.E1037D|PKHD1_uc003pai.3_Missense_Mutation_p.E3054D	NM_138694	NP_619639	P08F94	PKHD1_HUMAN	Homo sapiens polycystic kidney and hepatic disease 1 (autosomal recessive) (PKHD1), transcript variant 1, mRNA.	3054					cell-cell adhesion|cilium assembly|homeostatic process|kidney development|negative regulation of cellular component movement	anchored to external side of plasma membrane|apical plasma membrane|integral to membrane|microtubule basal body	protein binding|receptor activity			NS(1)|autonomic_ganglia(1)|breast(8)|central_nervous_system(5)|cervix(1)|endometrium(16)|haematopoietic_and_lymphoid_tissue(4)|kidney(11)|large_intestine(59)|lung(139)|ovary(16)|prostate(8)|skin(20)|soft_tissue(1)|stomach(2)|upper_aerodigestive_tract(7)|urinary_tract(5)	304	Lung NSC(77;0.0605)					AGGCCTGACCCTCTAAATCTA	0.498000													4	95					0	0	1	0	0
CD3G	917	broad.mit.edu	37	11	118223127	118223127	+	Silent	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr11:118223127G>A	uc001psu.2	+	5	572	c.492G>A	c.(490-492)aaG>aaA	p.K164K	CD3G_uc009zaa.1_Silent_p.K104K	NM_000073	NP_000064	P09693	CD3G_HUMAN	Homo sapiens CD3g molecule, gamma (CD3-TCR complex) (CD3G), mRNA.	164	ITAM.				T cell activation|T cell costimulation|T cell receptor signaling pathway|establishment or maintenance of cell polarity|protein complex assembly|protein transport|regulation of apoptosis	T cell receptor complex|integral to plasma membrane	T cell receptor binding|protein heterodimerization activity|receptor signaling complex scaffold activity|transmembrane receptor activity			breast(2)|kidney(1)|large_intestine(2)|skin(1)	6	all_hematologic(175;0.046)	Medulloblastoma(222;0.0425)|Breast(348;0.181)|all_hematologic(192;0.196)|all_neural(223;0.234)		BRCA - Breast invasive adenocarcinoma(274;3.04e-05)		AGCCCCTCAAGGATCGAGAAG	0.393000													74	118					0	0	1	0	0
SERPINB7	8710	broad.mit.edu	37	18	61471819	61471819	+	Missense_Mutation	SNP	A	A	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr18:61471819A>T	uc002ljl.3	+	7	1189	c.1093A>T	c.(1093-1095)Atc>Ttc	p.I365F	SERPINB7_uc002ljm.3_Missense_Mutation_p.I365F|SERPINB7_uc010xet.2_Missense_Mutation_p.I348F|SERPINB7_uc010dqg.3_Missense_Mutation_p.I365F	NM_001040147	NP_003775	O75635	SPB7_HUMAN	Homo sapiens serpin peptidase inhibitor, clade B (ovalbumin), member 7 (SERPINB7), transcript variant 2, mRNA.	365					regulation of proteolysis	cytoplasm	serine-type endopeptidase inhibitor activity			central_nervous_system(1)|endometrium(1)|kidney(4)|large_intestine(3)|lung(14)|prostate(1)|skin(3)	27		Esophageal squamous(42;0.129)				CCTATTTGTTATCAGGAAGGA	0.453000													4	90					0	0	1	0	0
ZZEF1	23140	broad.mit.edu	37	17	3917439	3917439	+	Silent	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr17:3917439G>T	uc002fxe.3	-	50	8422	c.8358C>A	c.(8356-8358)acC>acA	p.T2786T	ZZEF1_uc002fxg.1_Silent_p.T107T	NM_015113	NP_055928	O43149	ZZEF1_HUMAN	Homo sapiens zinc finger, ZZ-type with EF-hand domain 1 (ZZEF1), mRNA.	2786							calcium ion binding|zinc ion binding			central_nervous_system(1)|cervix(2)|endometrium(11)|haematopoietic_and_lymphoid_tissue(1)|kidney(9)|large_intestine(17)|lung(19)|ovary(3)|pancreas(1)|prostate(3)|skin(8)|stomach(1)|upper_aerodigestive_tract(5)|urinary_tract(3)	84						AGCCCCACTCGGTGTTGCTCA	0.582000													3	49					0	0	1	0	0
LCE1D	353134	broad.mit.edu	37	1	152770502	152770502	+	Missense_Mutation	SNP	C	C	T	rs142021851		TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:152770502C>T	uc021ozh.1	+	0	232	c.232C>T	c.(232-234)Cgc>Tgc	p.R78C	LCE1D_uc009wnp.3_Missense_Mutation_p.R78C	NM_178352	NP_848129	Q5T752	LCE1D_HUMAN	Homo sapiens late cornified envelope 1D (LCE1D), mRNA.	78	Cys-rich.		R -> H (in dbSNP:rs41268490).		cellular response to calcium ion|keratinization	cornified envelope|perinuclear region of cytoplasm				large_intestine(1)	1	Lung NSC(65;3.97e-29)|Hepatocellular(266;0.0877)|all_hematologic(923;0.127)|Melanoma(130;0.242)		LUSC - Lung squamous cell carcinoma(543;0.206)			CCACCACAGGCGCCACAGGTC	0.716000													6	67					0	0	1	0	0
OR4C11	219429	broad.mit.edu	37	11	55371343	55371343	+	Silent	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr11:55371343G>T	uc010rii.2	-	0	532	c.507C>A	c.(505-507)ccC>ccA	p.P169P		NM_001004700	NP_001004700	Q6IEV9	OR4CB_HUMAN	Homo sapiens olfactory receptor, family 4, subfamily C, member 11 (OR4C11), mRNA.	169					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			endometrium(1)|kidney(1)|large_intestine(5)|lung(23)|ovary(1)|prostate(1)|skin(1)	33						CAATCAAATAGGGTCCACAGA	0.448000													4	66					0	0	1	0	0
RBMY1B	378948	broad.mit.edu	37	Y	24050318	24050318	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chrY:24050318C>T	uc004fuw.4	-	11	1368	c.1216G>A	c.(1216-1218)Gca>Aca	p.A406T	RBMY1B_uc010nxc.1_Intron|RBMY1B_uc011nbg.2_Missense_Mutation_p.A369T|RBMY1B_uc010nxd.3_Missense_Mutation_p.A369T|RBMY1B_uc004fux.4_Missense_Mutation_p.A266T|RBMY1B_uc011nbf.2_Missense_Mutation_p.A334T	NM_001006121	NP_001006118	A6NDE4	RBY1B_HUMAN	Homo sapiens RNA binding motif protein, Y-linked, family 1, member B (RBMY1B), mRNA.	406					RNA splicing|mRNA processing|male gonad development|spermatogenesis	nucleus	RNA binding|nucleotide binding|protein binding										GGCCCTCTTGCAGGTGGTGCA	0.448000													12	98					0	0	1	0	0
SKIV2L	6499	broad.mit.edu	37	6	31936654	31936654	+	Silent	SNP	C	C	A	rs138923214		TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr6:31936654C>A	uc003nyn.1	+	25	3576	c.3187C>A	c.(3187-3189)Cga>Aga	p.R1063R	SKIV2L_uc011dou.1_Silent_p.R905R|SKIV2L_uc011dov.1_Silent_p.R870R|STK19_uc003nyt.3_5'Flank|STK19_uc011dow.2_5'Flank|STK19_uc011dox.1_5'Flank|STK19_uc003nyv.3_5'Flank|STK19_uc003nyw.3_5'Flank	NM_006929	NP_008860	Q15477	SKIV2_HUMAN	Homo sapiens superkiller viralicidic activity 2-like (S. cerevisiae) (SKIV2L), mRNA.	1063						nucleus	ATP binding|ATP-dependent RNA helicase activity|RNA binding|protein binding			breast(1)|central_nervous_system(1)|large_intestine(1)|ovary(1)	4						GCAGGTGCTCCGAACCCTGGG	0.607000													5	127					0	0	1	0	0
CTPS2	56474	broad.mit.edu	37	X	16720991	16720991	+	Nonsense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chrX:16720991G>T	uc004cxk.3	-	1	779	c.35C>A	c.(34-36)tCa>tAa	p.S12*	CTPS2_uc004cxl.3_Nonsense_Mutation_p.S12*|CTPS2_uc004cxm.3_Nonsense_Mutation_p.S12*	NM_001144002	NP_787055	Q9NRF8	PYRG2_HUMAN	Homo sapiens CTP synthase II (CTPS2), transcript variant 3, mRNA.	12					glutamine metabolic process|nucleobase, nucleoside and nucleotide interconversion|pyrimidine nucleotide biosynthetic process	cytosol	ATP binding|CTP synthase activity			breast(1)|endometrium(3)|large_intestine(4)|lung(6)|ovary(2)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	19	Hepatocellular(33;0.0997)					ACCAATGCCTGAGATGACCCC	0.438000													5	72					0	0	1	0	0
ANK1	286	broad.mit.edu	37	8	41557063	41557063	+	Missense_Mutation	SNP	T	T	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr8:41557063T>G	uc003xok.3	-	22	2549	c.2465A>C	c.(2464-2466)gAa>gCa	p.E822A	NKX6-3_uc010lxa.1_Intron|ANK1_uc003xoh.3_Missense_Mutation_p.E138A|ANK1_uc003xoi.3_Missense_Mutation_p.E822A|ANK1_uc003xoj.3_Missense_Mutation_p.E822A|ANK1_uc003xol.3_Missense_Mutation_p.E822A|ANK1_uc003xom.3_Missense_Mutation_p.E863A	NM_020476	NP_065209	P16157	ANK1_HUMAN	Homo sapiens ankyrin 1, erythrocytic (ANK1), transcript variant 1, mRNA.	822	89 kDa domain.				axon guidance|cytoskeleton organization|exocytosis|maintenance of epithelial cell apical/basal polarity|signal transduction	basolateral plasma membrane|cytosol|sarcomere|sarcoplasmic reticulum|spectrin-associated cytoskeleton	cytoskeletal adaptor activity|enzyme binding|protein binding|spectrin binding|structural constituent of cytoskeleton			breast(5)|central_nervous_system(4)|endometrium(9)|kidney(1)|large_intestine(26)|lung(62)|ovary(3)|prostate(5)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(3)	122	Ovarian(28;0.00541)|Colorectal(14;0.0398)|Lung SC(25;0.211)	all_lung(54;0.000626)|Lung NSC(58;0.00245)|Esophageal squamous(32;0.0559)|Hepatocellular(245;0.0663)|Renal(179;0.188)	OV - Ovarian serous cystadenocarcinoma(14;0.000984)|Lung(22;0.00108)|Colorectal(10;0.00245)|LUSC - Lung squamous cell carcinoma(45;0.00392)|COAD - Colon adenocarcinoma(11;0.0264)			GATGAGTTCTTCCCCTGAAAC	0.522000													50	155					0	0	1	0	0
MYOF	26509	broad.mit.edu	37	10	95089443	95089443	+	Missense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr10:95089443C>T	uc001kin.3	-	43	5083	c.4960G>A	c.(4960-4962)Ggc>Agc	p.G1654S	MYOF_uc001kio.3_Missense_Mutation_p.G1641S|MYOF_uc009xue.3_Non-coding_Transcript	NM_013451	NP_038479	Q9NZM1	MYOF_HUMAN	Homo sapiens myoferlin (MYOF), transcript variant 1, mRNA.	1654					blood circulation|muscle contraction|plasma membrane repair	caveola|cytoplasmic vesicle membrane|integral to membrane|nuclear membrane	phospholipid binding|protein binding			NS(2)|autonomic_ganglia(1)|breast(3)|endometrium(7)|kidney(7)|large_intestine(15)|lung(14)|ovary(4)|prostate(4)|skin(6)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	67						TCTGGTATGCCGCAGTGGGAC	0.483000													5	63					0	0	1	0	0
OR2M1P	388762	broad.mit.edu	37	1	248286050	248286050	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:248286050C>A	uc001idy.1	+	0	613	c.613C>A	c.(613-615)Ctg>Atg	p.L205M						Homo sapiens olfactory receptor, family 2, subfamily M, member 1 pseudogene (OR2M1P), non-coding RNA.																		GCAGGACAAGCTGGTGTCTGT	0.512000													6	164					0	0	1	0	0
FSTL5	56884	broad.mit.edu	37	4	162680679	162680679	+	Missense_Mutation	SNP	A	A	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:162680679A>G	uc003iqh.3	-	5	1047	c.611T>C	c.(610-612)aTa>aCa	p.I204T	FSTL5_uc003iqi.3_Missense_Mutation_p.I203T|FSTL5_uc010iqv.3_Missense_Mutation_p.I203T	NM_020116	NP_064501	Q8N475	FSTL5_HUMAN	Homo sapiens follistatin-like 5 (FSTL5), transcript variant 1, mRNA.	204	EF-hand 1.					extracellular region	calcium ion binding			central_nervous_system(1)|cervix(1)|endometrium(9)|haematopoietic_and_lymphoid_tissue(4)|kidney(3)|large_intestine(18)|lung(43)|ovary(4)|pancreas(2)|prostate(2)|skin(2)|upper_aerodigestive_tract(2)	91	all_hematologic(180;0.24)			COAD - Colon adenocarcinoma(41;0.179)		TTCCTGTTTTATCACCTAACA	0.274000													11	53					0	0	1	0	0
CSGALNACT2	55454	broad.mit.edu	37	10	43650664	43650664	+	Missense_Mutation	SNP	T	T	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr10:43650664T>A	uc001jan.3	+	1	402	c.67T>A	c.(67-69)Tgc>Agc	p.C23S	CSGALNACT2_uc001jam.1_Missense_Mutation_p.C23S	NM_018590	NP_061060	Q8N6G5	CGAT2_HUMAN	Homo sapiens chondroitin sulfate N-acetylgalactosaminyltransferase 2 (CSGALNACT2), mRNA.	23					chondroitin sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process|dermatan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process	Golgi cisterna membrane|integral to Golgi membrane	glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase activity|metal ion binding			endometrium(12)|kidney(3)|large_intestine(5)|lung(16)|ovary(1)|prostate(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	42						TGCTTTGCTCTGCAGTTTGGT	0.438000													5	84					0	0	1	0	0
DACH2	117154	broad.mit.edu	37	X	86068206	86068206	+	Missense_Mutation	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chrX:86068206G>A	uc004eew.2	+	8	1633	c.1463G>A	c.(1462-1464)cGa>cAa	p.R488Q	DACH2_uc004eex.2_Missense_Mutation_p.R475Q|DACH2_uc010nmq.2_Missense_Mutation_p.R354Q|DACH2_uc011mra.1_Missense_Mutation_p.R321Q|DACH2_uc010nmr.2_Missense_Mutation_p.R269Q|DACH2_uc004eey.3_Missense_Mutation_p.R181Q|DACH2_uc004eez.3_Missense_Mutation_p.R171Q	NM_053281	NP_001132987	Q96NX9	DACH2_HUMAN	Homo sapiens dachshund homolog 2 (Drosophila) (DACH2), transcript variant 1, mRNA.	488	DACHbox-C.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|nucleotide binding	p.L487Q(1)		breast(2)|central_nervous_system(3)|cervix(1)|endometrium(7)|kidney(6)|large_intestine(14)|lung(28)|ovary(5)|pancreas(1)|skin(1)|upper_aerodigestive_tract(3)	71						AAGGAGCTGCGACTGGAGCTC	0.413000													9	4					0	0	1	0	0
MAML3	55534	broad.mit.edu	37	4	140641036	140641036	+	Missense_Mutation	SNP	A	A	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:140641036A>T	uc021xsg.1	-	4	3610	c.2858T>A	c.(2857-2859)aTg>aAg	p.M953K	MGST2_uc021xsf.1_Intron|MGST2_uc010ioi.1_Intron|MAML3_uc011chd.1_Missense_Mutation_p.M416K	NM_018717	NP_061187	Q96JK9	MAML3_HUMAN	Homo sapiens mastermind-like 3 (Drosophila) (MAML3), mRNA.	949	Gln-rich.				Notch signaling pathway|positive regulation of transcription from RNA polymerase II promoter|transcription, DNA-dependent	nuclear speck	transcription coactivator activity			breast(1)|endometrium(7)|kidney(2)|large_intestine(1)|lung(9)|ovary(1)|prostate(2)|urinary_tract(2)	25	all_hematologic(180;0.162)					GACTGTTCCCATAAGGCTCTG	0.577000													55	79					0	0	1	0	0
PEG3	5178	broad.mit.edu	37	19	57328000	57328000	+	Missense_Mutation	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr19:57328000G>A	uc002qnu.2	-	6	2161	c.1810C>T	c.(1810-1812)Cgc>Tgc	p.R604C	PEG3_uc010ygr.1_Intron|PEG3_uc010ygq.1_Intron|PEG3_uc002qnr.2_Intron|PEG3_uc010etp.2_Intron|PEG3_uc010ygs.1_Intron|PEG3_uc002qnq.2_Intron|PEG3_uc002qnt.2_Missense_Mutation_p.R575C|PEG3_uc002qnv.2_Missense_Mutation_p.R604C|PEG3_uc002qnw.2_Missense_Mutation_p.R480C|PEG3_uc002qnx.2_Missense_Mutation_p.R478C|PEG3_uc010etr.2_Missense_Mutation_p.R604C	NM_001146186	NP_001139657	Q9GZU2	PEG3_HUMAN	Homo sapiens paternally expressed 3 (PEG3), transcript variant 4, mRNA.	604					apoptosis|viral reproduction	cytoplasm|nucleus	nucleic acid binding|sequence-specific DNA binding transcription factor activity|zinc ion binding	p.R604C(3)|p.R604H(1)		NS(1)|biliary_tract(4)|breast(2)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(9)|large_intestine(27)|lung(84)|ovary(8)|pancreas(5)|prostate(6)|skin(8)|stomach(2)|upper_aerodigestive_tract(6)	170		Colorectal(82;0.000256)|all_neural(62;0.103)|Ovarian(87;0.243)		GBM - Glioblastoma multiforme(193;0.0269)		GTTTCCCCGCGCtcacgttca	0.458000													5	39					0	0	1	0	0
ADCY9	115	broad.mit.edu	37	16	4163839	4163839	+	Silent	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr16:4163839G>T	uc002cvx.3	-	1	2144	c.1605C>A	c.(1603-1605)acC>acA	p.T535T		NM_001116	NP_001107	O60503	ADCY9_HUMAN	Homo sapiens adenylate cyclase 9 (ADCY9), mRNA.	535					activation of adenylate cyclase activity by G-protein signaling pathway|activation of phospholipase C activity|activation of protein kinase A activity|cellular response to glucagon stimulus|energy reserve metabolic process|inhibition of adenylate cyclase activity by G-protein signaling pathway|nerve growth factor receptor signaling pathway|synaptic transmission|transmembrane transport|water transport	integral to plasma membrane	ATP binding|adenylate cyclase activity|metal ion binding			breast(4)|central_nervous_system(1)|cervix(2)|endometrium(5)|kidney(3)|large_intestine(11)|lung(9)|ovary(5)|prostate(4)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1)	47						AGTATTTTGCGGTGGCCTCAG	0.502000													5	168					0	0	1	0	0
HEATR7A	727957	broad.mit.edu	37	8	145235404	145235404	+	Silent	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr8:145235404G>T	uc003zbk.4	+	6	777	c.540G>T	c.(538-540)acG>acT	p.T180T	HEATR7A_uc003zbg.2_Silent_p.T180T|HEATR7A_uc003zbi.4_Silent_p.T180T|HEATR7A_uc003zbh.4_Silent_p.T180T|HEATR7A_uc011lla.1_Silent_p.T180T|HEATR7A_uc010mft.3_Silent_p.T180T	NM_032450	NP_115826	Q8NDA8	HTR7A_HUMAN	Homo sapiens HEAT repeat containing 7A (HEATR7A), transcript variant 1, mRNA.	180							binding			endometrium(2)|kidney(2)|lung(3)|skin(1)	8						AGCAGGACACGGTGCGCGTGG	0.647000													4	73					0	0	1	0	0
GAA	2548	broad.mit.edu	37	17	78090908	78090908	+	Splice_Site	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr17:78090908G>T	uc002jxp.3	+	16	2698	c.2331_splice	c.e16+1	p.T777_splice	GAA_uc002jxo.3_Splice_Site_p.T777_splice|GAA_uc002jxq.3_Splice_Site_p.T777_splice	NM_000152	NP_001073272	P10253	LYAG_HUMAN	Homo sapiens glucosidase, alpha; acid (GAA), transcript variant 1, mRNA.	777					cardiac muscle contraction|diaphragm contraction|glycogen catabolic process|lysosome organization|tongue morphogenesis|vacuolar sequestering|ventricular cardiac muscle tissue morphogenesis	lysosomal membrane	carbohydrate binding|maltose alpha-glucosidase activity			autonomic_ganglia(1)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(2)|kidney(2)|lung(6)|ovary(2)|prostate(2)|skin(1)|stomach(1)|upper_aerodigestive_tract(1)	21	all_neural(118;0.117)		OV - Ovarian serous cystadenocarcinoma(97;0.0292)|BRCA - Breast invasive adenocarcinoma(99;0.139)		Acarbose(DB00284)	ACCTGCAGACGGTGAGTCTGG	0.662000													3	48					0	0	1	0	0
BAGE1	0	broad.mit.edu	37	GL000237.1	2582	2582	+	RNA	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chrGL000237.1:2582C>T	uc011mgu.1	-	0		c.105G>A								Homo sapiens B melanoma antigen variant f (BAGE1) mRNA, complete cds, alternatively spliced.																		cagagcgagacgagccacggt	0.607000													7	10					0	0	1	0	0
RTL1	388015	broad.mit.edu	37	14	101349274	101349274	+	Missense_Mutation	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr14:101349274G>A	uc010txj.1	-	0	1911	c.1852C>T	c.(1852-1854)Cct>Tct	p.P618S	MIR127_uc001yig.3_5'Flank|MIR432_uc021sce.1_5'Flank|MIR136_uc010txk.1_5'Flank	NM_001134888	NP_001128360	E9PKS8	E9PKS8_HUMAN	Homo sapiens retrotransposon-like 1 (RTL1), mRNA.	618										breast(1)|endometrium(5)|kidney(4)|large_intestine(1)|lung(5)|pancreas(1)|prostate(2)|skin(2)	21						GCACCCACAGGTTCCCAAGGC	0.542000													6	40					0	0	1	0	0
VCAM1	7412	broad.mit.edu	37	1	101188742	101188742	+	Missense_Mutation	SNP	C	C	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:101188742C>G	uc001dti.3	+	2	728	c.507C>G	c.(505-507)gaC>gaG	p.D169E	VCAM1_uc010ouj.2_Missense_Mutation_p.D107E|VCAM1_uc001dtj.3_Missense_Mutation_p.D169E	NM_001078	NP_001069	P19320	VCAM1_HUMAN	Homo sapiens vascular cell adhesion molecule 1 (VCAM1), transcript variant 1, mRNA.	169	Ig-like C2-type 2.				heterophilic cell-cell adhesion|interferon-gamma-mediated signaling pathway|interspecies interaction between organisms|leukocyte tethering or rolling|membrane to membrane docking|positive regulation of T cell proliferation|regulation of immune response	alpha9-beta1 integrin-vascular cell adhesion molecule-1 complex|apical part of cell|external side of plasma membrane|extracellular space|filopodium|integral to membrane|microvillus|podosome	cell adhesion molecule binding|integrin binding			central_nervous_system(3)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(11)|liver(1)|lung(27)|skin(4)|upper_aerodigestive_tract(2)|urinary_tract(1)	56		all_epithelial(167;3.83e-06)|all_lung(203;0.000485)|Lung NSC(277;0.0011)		Epithelial(280;0.0227)|all cancers(265;0.0276)|COAD - Colon adenocarcinoma(174;0.149)|Colorectal(144;0.169)|Lung(183;0.196)	Carvedilol(DB01136)	AGGATGCAGACAGGAAGTCCC	0.418000													13	43					0	0	1	0	0
SLC38A4	55089	broad.mit.edu	37	12	47163194	47163194	+	Missense_Mutation	SNP	G	G	C			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr12:47163194G>C	uc001rpi.2	-	14	1716	c.1317C>G	c.(1315-1317)atC>atG	p.I439M	SLC38A4_uc001rpj.2_Missense_Mutation_p.I439M	NM_018018	NP_060488	Q969I6	S38A4_HUMAN	Homo sapiens solute carrier family 38, member 4 (SLC38A4), transcript variant 1, mRNA.	439					cellular nitrogen compound metabolic process|sodium ion transport	integral to membrane|plasma membrane	amino acid transmembrane transporter activity|symporter activity			NS(1)|central_nervous_system(1)|endometrium(3)|kidney(2)|large_intestine(4)|lung(6)|ovary(3)|skin(1)	21	Lung SC(27;0.192)|Renal(347;0.236)					ATAACAGTGTGATCACTGATG	0.363000													12	60					0	0	1	0	0
ZNF599	148103	broad.mit.edu	37	19	35260439	35260439	+	Missense_Mutation	SNP	C	C	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr19:35260439C>G	uc010edn.1	-	1	428	c.40G>C	c.(40-42)Gtg>Ctg	p.V14L	ZNF599_uc010edm.2_5'UTR|ZNF599_uc010xsd.2_Non-coding_Transcript|ZNF599_uc010edo.2_Non-coding_Transcript	NM_001007248	NP_001007249	Q96NL3	ZN599_HUMAN	Homo sapiens zinc finger protein 599 (ZNF599), mRNA.	14	KRAB.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			endometrium(3)|large_intestine(10)|lung(8)|ovary(1)|pancreas(1)|skin(1)	24	all_lung(56;1.13e-07)|Lung NSC(56;1.81e-07)|Esophageal squamous(110;0.162)		LUSC - Lung squamous cell carcinoma(66;0.138)			GTCACAACCACGTCTTCAAAT	0.532000													3	115					0	0	1	0	0
FSCN3	29999	broad.mit.edu	37	7	127235651	127235651	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr7:127235651C>A	uc003vmd.2	+	1	654	c.435C>A	c.(433-435)caC>caA	p.H145Q	FSCN3_uc003vmc.1_Missense_Mutation_p.H100Q|FSCN3_uc011kog.1_Non-coding_Transcript|FSCN3_uc011koh.1_Missense_Mutation_p.H11Q|FSCN3_uc010llc.2_Missense_Mutation_p.H145Q	NM_020369	NP_065102	Q9NQT6	FSCN3_HUMAN	Homo sapiens fascin homolog 3, actin-bundling protein, testicular (Strongylocentrotus purpuratus) (FSCN3), mRNA.	145						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						TCCATGTCCACGTGATCCTCT	0.607000													4	70					0	0	1	0	0
CLINT1	9685	broad.mit.edu	37	5	157218974	157218974	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr5:157218974C>A	uc003lxj.2	-	9	1322	c.1117G>T	c.(1117-1119)Ggt>Tgt	p.G373C	CLINT1_uc003lxg.2_5'Flank|CLINT1_uc003lxh.2_5'UTR|CLINT1_uc003lxi.2_Missense_Mutation_p.G355C|CLINT1_uc011ddv.2_Missense_Mutation_p.G373C	NM_014666	NP_055481	Q14677	EPN4_HUMAN	Homo sapiens clathrin interactor 1 (CLINT1), transcript variant 2, mRNA.	373					endocytosis|post-Golgi vesicle-mediated transport	Golgi apparatus|clathrin-coated vesicle|cytosol|membrane|perinuclear region of cytoplasm	clathrin binding|lipid binding	p.G372D(1)		breast(1)|endometrium(2)|kidney(3)|large_intestine(2)|lung(9)|ovary(2)|pancreas(1)|urinary_tract(1)	21	Renal(175;0.00488)	Medulloblastoma(196;0.0354)|all_neural(177;0.138)	Kidney(164;0.000171)|KIRC - Kidney renal clear cell carcinoma(164;0.000785)			CTCCAGTCACCAAAGTCTCCA	0.468000													4	71					0	0	1	0	0
GPATCH1	55094	broad.mit.edu	37	19	33602720	33602720	+	Missense_Mutation	SNP	C	C	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr19:33602720C>G	uc002nug.1	+	11	1990	c.1676C>G	c.(1675-1677)gCa>gGa	p.A559G	GPATCH1_uc002nuh.1_5'Flank	NM_018025	NP_060495	Q9BRR8	GPTC1_HUMAN	Homo sapiens G patch domain containing 1 (GPATCH1), mRNA.	559						catalytic step 2 spliceosome	nucleic acid binding			breast(4)|cervix(1)|endometrium(3)|kidney(2)|large_intestine(7)|lung(15)|prostate(4)|skin(4)	40	Esophageal squamous(110;0.137)					CTGCTGTACGCATCTTCCCAT	0.607000													3	119					0	0	1	0	0
TAB1	10454	broad.mit.edu	37	22	39770548	39770548	+	Silent	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr22:39770548C>T	uc003axq.4	+	1	389	c.327C>T	c.(325-327)atC>atT	p.I109I	TAB1_uc003axo.4_Silent_p.I109I|TAB1_uc003axr.3_5'UTR|TAB1_uc003axs.4_Silent_p.I110I	NM_004711	NP_004702	Q15750	TAB1_HUMAN	Homo sapiens synaptogyrin 1 (SYNGR1), transcript variant 1a, mRNA.	0	PP2C-like.				I-kappaB kinase/NF-kappaB cascade|JNK cascade|MyD88-dependent toll-like receptor signaling pathway|MyD88-independent toll-like receptor signaling pathway|Toll signaling pathway|activation of MAPK activity|activation of MAPKKK activity|innate immune response|positive regulation of NF-kappaB transcription factor activity|stress-activated MAPK cascade|toll-like receptor 1 signaling pathway|toll-like receptor 2 signaling pathway|toll-like receptor 3 signaling pathway|toll-like receptor 4 signaling pathway	cytosol|endosome membrane	catalytic activity|protein binding			breast(1)|endometrium(2)|large_intestine(2)|lung(8)|urinary_tract(1)	14						TGTCCGACATCGGTGTCTCGG	0.632000													23	39					0	0	1	0	0
GPR132	29933	broad.mit.edu	37	14	105517704	105517704	+	Missense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr14:105517704G>T	uc001yqd.3	-	3	1669	c.770C>A	c.(769-771)cCg>cAg	p.P257Q	GPR132_uc001yqc.3_Missense_Mutation_p.P69Q|GPR132_uc001yqe.3_Missense_Mutation_p.P248Q	NM_013345	NP_037477	Q9UNW8	GP132_HUMAN	Homo sapiens G protein-coupled receptor 132 (GPR132), mRNA.	257					response to stress	integral to membrane|plasma membrane	G-protein coupled receptor activity			central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(2)|lung(7)|ovary(3)|stomach(1)|upper_aerodigestive_tract(1)	18		all_cancers(154;0.0953)|Melanoma(154;0.155)|all_epithelial(191;0.219)	OV - Ovarian serous cystadenocarcinoma(23;0.00778)|all cancers(16;0.00936)|Epithelial(46;0.0227)	Epithelial(152;0.02)|all cancers(159;0.0419)|OV - Ovarian serous cystadenocarcinoma(161;0.0521)		CAGGTGGTACGGGGCGAAGCA	0.577000													4	98					0	0	1	0	0
ZNF630	57232	broad.mit.edu	37	X	47919356	47919356	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chrX:47919356C>A	uc004div.4	-	4	727	c.475G>T	c.(475-477)Ggg>Tgg	p.G159W	ZNF630_uc010nhz.1_Intron|ZNF630_uc022bvr.1_Missense_Mutation_p.G145W|ZNF630_uc022bvs.1_Missense_Mutation_p.G159W	NM_001037735	NP_001032824	Q2M218	ZN630_HUMAN	Homo sapiens zinc finger protein 630 (ZNF630), transcript variant 1, mRNA.	159					regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|zinc ion binding			endometrium(1)|large_intestine(6)|lung(11)|ovary(1)	19						AACATTTTCCCAAATGCACTG	0.388000													3	29					0	0	1	0	0
EGFR	1956	broad.mit.edu	37	7	55240710	55240710	+	Missense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr7:55240710G>T	uc003tqk.3	+	16	2200	c.1954G>T	c.(1954-1956)Ggg>Tgg	p.G652W	EGFR_uc022adm.1_Missense_Mutation_p.G652W|EGFR_uc010kzg.2_Missense_Mutation_p.G607W|EGFR_uc022adn.1_Missense_Mutation_p.G607W|EGFR_uc011kco.2_Missense_Mutation_p.G599W	NM_005228	NP_005219	P00533	EGFR_HUMAN	Homo sapiens epidermal growth factor receptor (EGFR), transcript variant 1, mRNA.	652					activation of phospholipase A2 activity by calcium-mediated signaling|activation of phospholipase C activity|axon guidance|cell proliferation|cell-cell adhesion|negative regulation of apoptosis|negative regulation of epidermal growth factor receptor signaling pathway|ossification|positive regulation of MAP kinase activity|positive regulation of catenin import into nucleus|positive regulation of cell migration|positive regulation of cyclin-dependent protein kinase activity involved in G1/S|positive regulation of epithelial cell proliferation|positive regulation of nitric oxide biosynthetic process|positive regulation of phosphorylation|positive regulation of protein kinase B signaling cascade|protein autophosphorylation|protein insertion into membrane|regulation of nitric-oxide synthase activity|regulation of peptidyl-tyrosine phosphorylation|response to UV-A|response to stress	Golgi membrane|Shc-EGFR complex|basolateral plasma membrane|endoplasmic reticulum membrane|endosome|extracellular space|integral to membrane|nuclear membrane	ATP binding|MAP/ERK kinase kinase activity|actin filament binding|double-stranded DNA binding|epidermal growth factor receptor activity|identical protein binding|protein heterodimerization activity|protein phosphatase binding|receptor signaling protein tyrosine kinase activity	p.V651M(2)|p.G652G(1)		NS(2)|adrenal_gland(5)|biliary_tract(8)|bone(3)|breast(18)|central_nervous_system(106)|endometrium(26)|eye(3)|haematopoietic_and_lymphoid_tissue(9)|kidney(11)|large_intestine(85)|liver(2)|lung(13575)|oesophagus(21)|ovary(38)|pancreas(3)|peritoneum(11)|pleura(2)|prostate(35)|salivary_gland(11)|skin(9)|small_intestine(1)|soft_tissue(4)|stomach(41)|thymus(2)|thyroid(14)|upper_aerodigestive_tract(59)|urinary_tract(6)	14110	all_cancers(1;1.57e-46)|all_epithelial(1;5.62e-37)|Lung NSC(1;9.29e-25)|all_lung(1;4.39e-23)|Esophageal squamous(2;7.55e-08)|Breast(14;0.0318)		GBM - Glioblastoma multiforme(1;0)|all cancers(1;2.19e-314)|Lung(13;4.65e-05)|LUSC - Lung squamous cell carcinoma(13;0.000168)|STAD - Stomach adenocarcinoma(5;0.00164)|Epithelial(13;0.0607)		Cetuximab(DB00002)|Erlotinib(DB00530)|Gefitinib(DB00317)|Lapatinib(DB01259)|Lidocaine(DB00281)|Panitumumab(DB01269)|Trastuzumab(DB00072)	TGGGATGGTGGGGGCCCTCCT	0.622000		8	"""A, O, Mis"""		"""glioma, NSCLC"""	NSCLC			Lung Cancer, Familial Clustering of	TCGA GBM(3;<1E-08)|TSP Lung(4;<1E-08)			5	106					0	0	1	0	0
AIMP1	9255	broad.mit.edu	37	4	107252942	107252942	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:107252942C>A	uc003hyh.3	+	4	618	c.577C>A	c.(577-579)Cct>Act	p.P193T	AIMP1_uc011cfg.2_Missense_Mutation_p.P169T|AIMP1_uc003hyg.3_Missense_Mutation_p.P169T	NM_001142416	NP_004748	Q12904	AIMP1_HUMAN	Homo sapiens aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 (AIMP1), transcript variant 3, mRNA.	169	Interaction with HSP90B1 (By similarity).|tRNA-binding.				angiogenesis|apoptosis|cell adhesion|cell-cell signaling|chemotaxis|glucose metabolic process|inflammatory response|leukocyte migration|negative regulation of endothelial cell proliferation|signal transduction|tRNA aminoacylation for protein translation	Golgi apparatus|aminoacyl-tRNA synthetase multienzyme complex|cytosol|endoplasmic reticulum|extracellular space|nucleus|transport vesicle	cell surface binding|cytokine activity|protein homodimerization activity|tRNA binding			breast(1)|endometrium(2)|kidney(1)|lung(5)|skin(1)|urinary_tract(1)	11						TAGAAAACACCCTGATGCAGA	0.443000													7	233					0	0	1	0	0
SNRPD3	6634	broad.mit.edu	37	22	24964015	24964015	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr22:24964015C>A	uc003aam.1	+	2	630	c.190C>A	c.(190-192)Cgt>Agt	p.R64S	SNRPD3_uc011aju.2_Missense_Mutation_p.R64S	NM_004175	NP_004166	P62318	SMD3_HUMAN	Homo sapiens small nuclear ribonucleoprotein D3 polypeptide 18kDa (SNRPD3), mRNA.	64					histone mRNA metabolic process|ncRNA metabolic process|spliceosomal snRNP assembly|termination of RNA polymerase II transcription	U12-type spliceosomal complex|U7 snRNP|catalytic step 2 spliceosome|cytosol|nucleoplasm	enzyme binding|histone pre-mRNA DCP binding			endometrium(1)|large_intestine(1)|lung(2)|ovary(1)|skin(1)	6						GGTATACATCCGTGGCAGCAA	0.478000													5	113					0	0	1	0	0
DCHS2	54798	broad.mit.edu	37	4	155157178	155157178	+	Missense_Mutation	SNP	A	A	G			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr4:155157178A>G	uc003inw.2	-	24	7261	c.7261T>C	c.(7261-7263)Ttt>Ctt	p.F2421L		NM_017639	NP_060109	Q6V1P9	PCD23_HUMAN	Homo sapiens dachsous 2 (Drosophila) (DCHS2), transcript variant 1, mRNA.	2421	Cadherin 21.				homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			NS(1)|breast(2)|central_nervous_system(1)|cervix(3)|endometrium(8)|kidney(5)|large_intestine(54)|lung(63)|ovary(4)|pancreas(1)|prostate(14)|skin(12)|stomach(4)|upper_aerodigestive_tract(2)|urinary_tract(2)	176	all_hematologic(180;0.208)	Renal(120;0.0854)		LUSC - Lung squamous cell carcinoma(193;0.107)		ATGGGCTCAAATTCATCTATC	0.433000													3	53					0	0	1	0	0
RGS6	9628	broad.mit.edu	37	14	72976881	72976881	+	Nonsense_Mutation	SNP	C	C	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr14:72976881C>T	uc001xna.4	+	13	1508	c.985C>T	c.(985-987)Cga>Tga	p.R329*	RGS6_uc021rvv.1_Nonsense_Mutation_p.R294*|RGS6_uc010ttn.2_Nonsense_Mutation_p.R329*|RGS6_uc021rvw.1_Nonsense_Mutation_p.R329*|RGS6_uc021rvx.1_Nonsense_Mutation_p.R329*|RGS6_uc021rvy.1_Nonsense_Mutation_p.R292*|RGS6_uc021rvz.1_Nonsense_Mutation_p.R292*|RGS6_uc001xmy.4_Nonsense_Mutation_p.R329*|RGS6_uc010tto.2_Non-coding_Transcript|RGS6_uc001xmx.4_Nonsense_Mutation_p.R329*|RGS6_uc021rwa.1_Nonsense_Mutation_p.R292*|RGS6_uc021rwb.1_Nonsense_Mutation_p.R292*|RGS6_uc010ttp.1_Nonsense_Mutation_p.R260*|RGS6_uc021rwc.1_Nonsense_Mutation_p.R190*	NM_001204423	NP_001191352	P49758	RGS6_HUMAN	Homo sapiens regulator of G-protein signaling 6 (RGS6), transcript variant 9, mRNA.	329	G protein gamma.				G-protein coupled receptor protein signaling pathway|intracellular signal transduction|negative regulation of signal transduction|regulation of G-protein coupled receptor protein signaling pathway	cytoplasm|heterotrimeric G-protein complex	GTPase activator activity|signal transducer activity			endometrium(2)|kidney(3)|large_intestine(6)|lung(14)|prostate(2)|skin(3)|upper_aerodigestive_tract(2)|urinary_tract(1)	33				all cancers(60;0.00309)|BRCA - Breast invasive adenocarcinoma(234;0.0281)|STAD - Stomach adenocarcinoma(64;0.0302)|OV - Ovarian serous cystadenocarcinoma(108;0.0476)		CAGCCAACAGCGAGTAAAAAG	0.458000													6	191					0	0	1	0	0
SHCBP1L	81626	broad.mit.edu	37	1	182873376	182873376	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:182873376C>A	uc001gpu.3	-	7	1811	c.1526G>T	c.(1525-1527)gGa>gTa	p.G509V	SHCBP1L_uc001gpv.3_Missense_Mutation_p.G390V|SHCBP1L_uc010pnz.2_Missense_Mutation_p.G367V|SHCBP1L_uc001gpw.3_Missense_Mutation_p.G229V	NM_030933	NP_112195	Q9BZQ2	SHP1L_HUMAN	Homo sapiens SHC SH2-domain binding protein 1-like (SHCBP1L), mRNA.	581										breast(1)|endometrium(2)|kidney(2)|large_intestine(3)|liver(1)|lung(2)|pancreas(1)|prostate(1)|skin(2)	15						AACACACACTCCTGTTCCTTC	0.408000													5	77					0	0	1	0	0
SP110	3431	broad.mit.edu	37	2	231033887	231033887	+	Missense_Mutation	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr2:231033887G>A	uc002vqg.3	-	18	2335	c.2095C>T	c.(2095-2097)Ctc>Ttc	p.L699F	SP110_uc002vqh.3_Missense_Mutation_p.L675F	NM_080424	NP_536349	Q9HB58	SP110_HUMAN	Homo sapiens SP110 nuclear body protein (SP110), transcript variant c, mRNA.	675					interspecies interaction between organisms|regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	DNA binding|signal transducer activity|zinc ion binding			breast(4)|endometrium(3)|large_intestine(5)|lung(8)|ovary(2)|prostate(1)|skin(2)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	29		Renal(207;0.0112)|all_lung(227;0.0223)|Lung NSC(271;0.0983)|all_hematologic(139;0.104)|Acute lymphoblastic leukemia(138;0.169)		Epithelial(121;2.61e-12)|all cancers(144;6.39e-10)|LUSC - Lung squamous cell carcinoma(224;0.008)|Lung(119;0.0097)		TGAAAACCGAGCACGTCTTTG	0.458000													74	151					0	0	1	0	0
FAM53B	9679	broad.mit.edu	37	10	126370648	126370648	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr10:126370648C>A	uc001lhv.1	-	3	957	c.434G>T	c.(433-435)cGc>cTc	p.R145L	FAM53B_uc001lhu.1_Missense_Mutation_p.R145L|FAM53B_uc001lhw.3_Missense_Mutation_p.R145L	NM_014661	NP_055476	Q14153	FA53B_HUMAN	Homo sapiens family with sequence similarity 53, member B (FAM53B), mRNA.	145										cervix(1)|lung(5)|ovary(2)|pancreas(1)	9		all_lung(145;0.0191)|Lung NSC(174;0.0301)|Colorectal(57;0.106)|all_neural(114;0.117)		COAD - Colon adenocarcinoma(40;0.141)|Colorectal(40;0.15)		GCTGTAGCAGCGTCTCTTTTC	0.617000													3	43					0	0	1	0	0
CFL2	1073	broad.mit.edu	37	14	35182678	35182678	+	Missense_Mutation	SNP	C	C	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr14:35182678C>A	uc001wsh.3	-	1	376	c.93G>T	c.(91-93)aaG>aaT	p.K31N	CFL2_uc001wsg.3_Missense_Mutation_p.K31N|CFL2_uc010tpn.1_Missense_Mutation_p.K14N|CFL2_uc001wsi.3_Intron|CFL2_uc001wsj.3_Non-coding_Transcript	NM_138638	NP_001230574	Q9Y281	COF2_HUMAN	Homo sapiens cofilin 2 (muscle) (CFL2), transcript variant 2, mRNA.	31	ADF-H.					cytoplasm|cytoskeleton|nuclear matrix	actin binding			breast(3)|endometrium(2)|lung(3)	8	Breast(36;0.0361)|Hepatocellular(127;0.158)		LUAD - Lung adenocarcinoma(48;6.07e-06)|Lung(238;2.23e-05)|Epithelial(34;0.0387)|all cancers(34;0.0814)	GBM - Glioblastoma multiforme(112;0.0424)		CTTTCTTTCTCTTTTTGATCT	0.353000													4	57					0	0	1	0	0
NLRP14	338323	broad.mit.edu	37	11	7064143	7064143	+	Missense_Mutation	SNP	G	G	T			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr11:7064143G>T	uc001mfb.1	+	3	1209	c.886G>T	c.(886-888)Gtg>Ttg	p.V296L		NM_176822	NP_789792	Q86W24	NAL14_HUMAN	Homo sapiens NLR family, pyrin domain containing 14 (NLRP14), mRNA.	296	NACHT.				cell differentiation|multicellular organismal development|spermatogenesis		ATP binding			breast(3)|large_intestine(7)|lung(1)|ovary(3)|pancreas(1)|skin(3)|stomach(1)|upper_aerodigestive_tract(2)	21				Epithelial(150;4.62e-08)|BRCA - Breast invasive adenocarcinoma(625;0.0871)		GCTGAGGAAAGTGATGCTCCC	0.448000													13	53					0	0	1	0	0
PRAMEF11	440560	broad.mit.edu	37	1	12884845	12884845	+	Silent	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr1:12884845G>A	uc001auk.2	-	3	1462	c.1266C>T	c.(1264-1266)ggC>ggT	p.G422G		NM_001146344	NP_001139816	O60813	PRA11_HUMAN	Homo sapiens PRAME family member 11 (PRAMEF11), mRNA.	422										NS(1)|endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|lung(7)|pancreas(2)|skin(4)|urinary_tract(1)	27						ATGACCTGTCGCCATGGTCAG	0.473000													11	367					0	0	1	0	0
ANKS1B	56899	broad.mit.edu	37	12	99837459	99837459	+	Nonsense_Mutation	SNP	G	G	A			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr12:99837459G>A	uc001tge.2	-	10	1984	c.1567C>T	c.(1567-1569)Cga>Tga	p.R523*	ANKS1B_uc001tgf.2_Nonsense_Mutation_p.R103*|ANKS1B_uc009ztt.1_Nonsense_Mutation_p.R489*	NM_152788	NP_690001	Q7Z6G8	ANS1B_HUMAN	Homo sapiens ankyrin repeat and sterile alpha motif domain containing 1B (ANKS1B), transcript variant 1, mRNA.	523						Cajal body|cell junction|cytoplasm|dendritic spine|postsynaptic density|postsynaptic membrane				NS(1)|breast(1)|cervix(1)|endometrium(4)|kidney(6)|large_intestine(15)|lung(38)|pancreas(1)|prostate(2)|skin(1)	70		all_cancers(3;0.0197)|all_epithelial(3;0.0101)|Esophageal squamous(3;0.0559)|Breast(359;0.209)		OV - Ovarian serous cystadenocarcinoma(2;2.89e-08)|Epithelial(2;6.12e-08)|all cancers(2;4.07e-06)		ACCTGGGGTCGAATGACTTTT	0.423000													4	84					0	0	1	0	0
CEBPB	1051	broad.mit.edu	37	20	48807874	48807885	+	In_Frame_Del	DEL	CCCGCGCCCGCC	-	-			TCGA-HC-7075-01A-11D-1961-08	TCGA-HC-7075-10A-01D-1961-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	ddc422e4-87e2-4fc0-b56b-ddc2d6a92f58	f10cbfd4-a508-4061-a2b0-767db51dc211	g.chr20:48807874_48807885delCCCGCGCCCGCC	uc002xvi.2	+	0	755_766	c.304_315delCCCGCGCCCGCC	c.(304-315)cccgcgcccgccdel	p.PAPA106del		NM_005194	NP_005185	P17676	CEBPB_HUMAN	Homo sapiens CCAAT/enhancer binding protein (C/EBP), beta (CEBPB), mRNA.	106					acute-phase response|immune response		sequence-specific enhancer binding RNA polymerase II transcription factor activity			NS(1)|lung(1)	2			BRCA - Breast invasive adenocarcinoma(9;5.72e-08)|STAD - Stomach adenocarcinoma(23;0.19)			GGCGGCTccgcccgcgcccgcccccgcgcccg	0.745													3	3	---	---	---	---					
