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
C8B	732	broad.mit.edu	37	1	57406638	57406638	+	Nonsense_Mutation	SNP	G	G	A	rs41286844	byFrequency	TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:57406638G>A	uc001cyp.3	-	8	1349	c.1282C>T	c.(1282-1284)Cga>Tga	p.R428*	C8B_uc010oon.2_Nonsense_Mutation_p.R366*|C8B_uc010ooo.2_Nonsense_Mutation_p.R376*	NM_000066	NP_000057	P07358	CO8B_HUMAN	Homo sapiens complement component 8, beta polypeptide (C8B), mRNA.	428	MACPF.				complement activation, alternative pathway|complement activation, classical pathway|cytolysis	membrane attack complex		p.R428Q(1)		breast(2)|central_nervous_system(2)|endometrium(5)|kidney(2)|large_intestine(11)|liver(1)|lung(20)|ovary(1)|prostate(1)|skin(6)|upper_aerodigestive_tract(1)	52						GCCCCTCCTCGTACCAGGACC	0.587												
HRNR	388697	broad.mit.edu	37	1	152187663	152187663	+	Nonsense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:152187663G>A	uc001ezt.1	-	2	6518	c.6442C>T	c.(6442-6444)Cga>Tga	p.R2148*		NM_001009931	NP_001009931	Q86YZ3	HORN_HUMAN	Homo sapiens hornerin (HRNR), mRNA.	2148					keratinization		calcium ion binding|protein binding	p.R2148*(2)|p.R2148L(1)		autonomic_ganglia(1)|breast(6)|central_nervous_system(2)|cervix(2)|endometrium(22)|haematopoietic_and_lymphoid_tissue(1)|kidney(11)|large_intestine(19)|liver(1)|lung(84)|ovary(5)|prostate(6)|skin(12)|stomach(9)|upper_aerodigestive_tract(5)|urinary_tract(6)	192	Hepatocellular(266;0.0877)|Melanoma(130;0.116)|all_hematologic(923;0.127)		LUSC - Lung squamous cell carcinoma(543;0.206)			GATCCGTGTCGTTCACCCCTA	0.587												
MEF2D	4209	broad.mit.edu	37	1	156446904	156446904	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:156446904G>A	uc001fpc.3	-	6	1145	c.755C>T	c.(754-756)cCa>cTa	p.P252L	MEF2D_uc001fpb.3_Missense_Mutation_p.P252L|MEF2D_uc001fpd.3_Missense_Mutation_p.P252L|MEF2D_uc009wsa.3_Non-coding_Transcript|MEF2D_uc001fpe.1_Missense_Mutation_p.P252L	NM_005920	NP_005911	Q14814	MEF2D_HUMAN	Homo sapiens myocyte enhancer factor 2D (MEF2D), mRNA.	252	Poly-Pro.				apoptosis|muscle organ development|nervous system development|positive regulation of transcription from RNA polymerase II promoter	nucleus	activating transcription factor binding|histone deacetylase binding|RNA polymerase II regulatory region sequence-specific DNA binding|sequence-specific DNA binding RNA polymerase II transcription factor activity			endometrium(4)|kidney(1)|large_intestine(2)|lung(6)|ovary(1)|urinary_tract(1)	15	all_hematologic(923;0.088)|Hepatocellular(266;0.158)					AGGTGGGGGTGGAGACTTGGC	0.607												
FCER1A	2205	broad.mit.edu	37	1	159275846	159275846	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:159275846G>A	uc001ftq.3	+	4	497	c.400G>A	c.(400-402)Ggt>Agt	p.G134S		NM_002001	NP_001992	P12319	FCERA_HUMAN	Homo sapiens Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide (FCER1A), mRNA.	134	Ig-like 2.					integral to plasma membrane				autonomic_ganglia(1)|central_nervous_system(1)|endometrium(2)|large_intestine(3)|lung(19)|prostate(2)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1)	33	all_hematologic(112;0.0429)				Benzylpenicilloyl Polylysine(DB00895)|Omalizumab(DB00043)	CAGGTGCCATGGTTGGAGGAA	0.468												
DUSP27	92235	broad.mit.edu	37	1	167097485	167097485	+	Silent	SNP	C	C	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:167097485C>A	uc001geb.1	+	4	3133	c.3117C>A	c.(3115-3117)ccC>ccA	p.P1039P		NM_001080426	NP_001073895	Q5VZP5	DUS27_HUMAN	Homo sapiens dual specificity phosphatase 27 (putative) (DUSP27), mRNA.	1039					protein dephosphorylation		protein tyrosine/serine/threonine phosphatase activity			NS(1)|breast(1)|central_nervous_system(1)|cervix(1)|endometrium(4)|haematopoietic_and_lymphoid_tissue(4)|kidney(2)|large_intestine(11)|liver(1)|lung(46)|ovary(5)|prostate(5)|skin(4)|upper_aerodigestive_tract(3)	89						GCCCAGAGCCCTACTTCTTCC	0.587												
HMCN1	83872	broad.mit.edu	37	1	185878633	185878633	+	Missense_Mutation	SNP	T	T	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:185878633T>A	uc001grq.1	+	4	1015	c.786T>A	c.(784-786)aaT>aaA	p.N262K		NM_031935	NP_114141	Q96RW7	HMCN1_HUMAN	Homo sapiens hemicentin 1 (HMCN1), mRNA.	262					response to stimulus|visual perception	basement membrane	calcium ion binding	p.R261H(1)		NS(2)|autonomic_ganglia(1)|breast(10)|central_nervous_system(2)|cervix(1)|endometrium(28)|haematopoietic_and_lymphoid_tissue(4)|kidney(13)|large_intestine(58)|liver(3)|lung(101)|ovary(23)|pancreas(4)|prostate(20)|skin(8)|stomach(1)|upper_aerodigestive_tract(11)|urinary_tract(18)	308						AAATTCGCAATCCTTTAGGTG	0.363												
LAMB3	3914	broad.mit.edu	37	1	209790792	209790792	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:209790792G>A	uc001hhg.3	-	19	3581	c.3191C>T	c.(3190-3192)gCg>gTg	p.A1064V	LAMB3_uc009xco.3_Missense_Mutation_p.A1064V|LAMB3_uc001hhh.3_Missense_Mutation_p.A1064V	NM_001017402	NP_001121113	Q13751	LAMB3_HUMAN	Homo sapiens laminin, beta 3 (LAMB3), transcript variant 2, mRNA.	1064	Domain I.				cell adhesion|epidermis development|hemidesmosome assembly		structural molecule activity			NS(1)|breast(3)|central_nervous_system(2)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(11)|lung(13)|ovary(1)|prostate(1)|skin(4)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	45				OV - Ovarian serous cystadenocarcinoma(81;0.0519)		GGCACCTTCCGCAAGCTGCTG	0.627												
LAMB3	3914	broad.mit.edu	37	1	209801465	209801465	+	Missense_Mutation	SNP	G	G	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:209801465G>C	uc001hhg.3	-	9	1593	c.1203C>G	c.(1201-1203)tgC>tgG	p.C401W	LAMB3_uc009xco.3_Missense_Mutation_p.C401W|LAMB3_uc001hhh.3_Missense_Mutation_p.C401W|LAMB3_uc010psl.1_Non-coding_Transcript	NM_001017402	NP_001121113	Q13751	LAMB3_HUMAN	Homo sapiens laminin, beta 3 (LAMB3), transcript variant 2, mRNA.	401	Laminin EGF-like 3.				cell adhesion|epidermis development|hemidesmosome assembly		structural molecule activity			NS(1)|breast(3)|central_nervous_system(2)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(11)|lung(13)|ovary(1)|prostate(1)|skin(4)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1)	45				OV - Ovarian serous cystadenocarcinoma(81;0.0519)		CATGCTCCTTGCACACACACT	0.642											OREG0014217	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
DIEXF	27042	broad.mit.edu	37	1	210001468	210001468	+	Missense_Mutation	SNP	G	G	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:210001468G>C	uc001hhr.2	+	0	157	c.60G>C	c.(58-60)caG>caC	p.Q20H	DIEXF_uc009xcu.2_5'UTR	NM_014388	NP_055203	Q68CQ4	DIEXF_HUMAN	Homo sapiens digestive organ expansion factor homolog (zebrafish) (DIEXF), mRNA.	20					multicellular organismal development	nucleus				breast(6)|central_nervous_system(2)|cervix(2)|endometrium(2)|kidney(15)|large_intestine(7)|lung(12)|ovary(1)|skin(3)|stomach(1)|urinary_tract(2)	53						CTAAAAAGCAGAAGAAACATC	0.547											OREG0014221	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
DIEXF	27042	broad.mit.edu	37	1	210001493	210001493	+	Nonsense_Mutation	SNP	G	G	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:210001493G>T	uc001hhr.2	+	0	182	c.85G>T	c.(85-87)Gag>Tag	p.E29*	DIEXF_uc009xcu.2_5'UTR	NM_014388	NP_055203	Q68CQ4	DIEXF_HUMAN	Homo sapiens digestive organ expansion factor homolog (zebrafish) (DIEXF), mRNA.	29					multicellular organismal development	nucleus				breast(6)|central_nervous_system(2)|cervix(2)|endometrium(2)|kidney(15)|large_intestine(7)|lung(12)|ovary(1)|skin(3)|stomach(1)|urinary_tract(2)	53						AGATTTCGGCGAGGAGCATCC	0.547											OREG0014221	type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip)
PGBD2	267002	broad.mit.edu	37	1	249212387	249212387	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:249212387G>A	uc001ifh.3	+	2	1751	c.1604G>A	c.(1603-1605)gGg>gAg	p.G535E	PGBD2_uc001ifg.3_Missense_Mutation_p.G284E|PGBD2_uc009xhd.3_Missense_Mutation_p.G532E|PGBD2_uc021pmh.1_Missense_Mutation_p.G284E	NM_170725	NP_001017434	Q6P3X8	PGBD2_HUMAN	Homo sapiens piggyBac transposable element derived 2 (PGBD2), transcript variant 1, mRNA.	535										NS(1)|endometrium(3)|lung(6)|ovary(1)|skin(3)	14	all_cancers(71;3.33e-06)|all_epithelial(71;2.41e-06)|Breast(184;0.00909)|Ovarian(71;0.0377)|all_lung(81;0.0458)|Lung NSC(105;0.0494)|Melanoma(84;0.199)	all_cancers(173;0.012)	OV - Ovarian serous cystadenocarcinoma(106;0.00989)			ACATCTCAAGGGAGGCGAAGC	0.547												
PGBD2	267002	broad.mit.edu	37	1	249212544	249212544	+	Missense_Mutation	SNP	G	G	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr1:249212544G>T	uc001ifh.3	+	2	1908	c.1761G>T	c.(1759-1761)agG>agT	p.R587S	PGBD2_uc001ifg.3_Missense_Mutation_p.R336S|PGBD2_uc009xhd.3_Missense_Mutation_p.R584S|PGBD2_uc021pmh.1_Missense_Mutation_p.R336S	NM_170725	NP_001017434	Q6P3X8	PGBD2_HUMAN	Homo sapiens piggyBac transposable element derived 2 (PGBD2), transcript variant 1, mRNA.	587										NS(1)|endometrium(3)|lung(6)|ovary(1)|skin(3)	14	all_cancers(71;3.33e-06)|all_epithelial(71;2.41e-06)|Breast(184;0.00909)|Ovarian(71;0.0377)|all_lung(81;0.0458)|Lung NSC(105;0.0494)|Melanoma(84;0.199)	all_cancers(173;0.012)	OV - Ovarian serous cystadenocarcinoma(106;0.00989)			AATGCTTCAGGGAGTACCACA	0.478												
LBX1	10660	broad.mit.edu	37	10	102987489	102987489	+	Silent	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr10:102987489C>T	uc001ksx.3	-	1	529	c.384G>A	c.(382-384)tcG>tcA	p.S128S	FLJ41350_uc010qpy.2_5'Flank	NM_006562	NP_006553	P52954	LBX1_HUMAN	Homo sapiens ladybird homeobox 1 (LBX1), mRNA.	128					muscle organ development		sequence-specific DNA binding			large_intestine(2)|lung(4)|ovary(1)	7		Colorectal(252;0.234)		Epithelial(162;3.22e-09)|all cancers(201;1.79e-07)		AGGCCGTGCGCGACTTTCGCC	0.587												
OR52B2	255725	broad.mit.edu	37	11	6190634	6190634	+	Missense_Mutation	SNP	C	C	T	rs147668114	by1000genomes	TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr11:6190634C>T	uc010qzy.2	-	0	923	c.923G>A	c.(922-924)cGg>cAg	p.R308Q		NM_001004052	NP_001004052	Q96RD2	O52B2_HUMAN	Homo sapiens olfactory receptor, family 52, subfamily B, member 2 (OR52B2), mRNA.	308					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity	p.R308Q(3)|p.R308R(1)		NS(1)|central_nervous_system(3)|endometrium(1)|large_intestine(1)|lung(15)	21		Medulloblastoma(188;0.00776)|all_neural(188;0.0652)|Breast(177;0.114)		Epithelial(150;3.69e-08)|BRCA - Breast invasive adenocarcinoma(625;0.135)		GTCAAAGAACCGGTGGGCTAC	0.478												
INSC	387755	broad.mit.edu	37	11	15260573	15260573	+	Missense_Mutation	SNP	G	G	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr11:15260573G>C	uc001mlz.3	+	10	1457	c.1346G>C	c.(1345-1347)cGt>cCt	p.R449P	INSC_uc001mly.3_Missense_Mutation_p.R496P|INSC_uc001mma.3_Missense_Mutation_p.R449P|INSC_uc010rcs.2_Missense_Mutation_p.R484P|INSC_uc001mmb.3_Missense_Mutation_p.R449P|INSC_uc001mmc.3_Missense_Mutation_p.R407P	NM_001042536	NP_001036001	Q1MX18	INSC_HUMAN	Homo sapiens inscuteable homolog (Drosophila) (INSC), transcript variant 2, mRNA.	496					cell differentiation|nervous system development	cytoplasm	binding			NS(2)|breast(1)|central_nervous_system(2)|endometrium(6)|kidney(4)|large_intestine(3)|lung(24)|ovary(3)|skin(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	49						ACCCTGGCTCGTCTCAGCCGA	0.607												
HIPK3	10114	broad.mit.edu	37	11	33362619	33362619	+	Missense_Mutation	SNP	C	C	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr11:33362619C>A	uc001mul.1	+	6	1989	c.1719C>A	c.(1717-1719)agC>agA	p.S573R	HIPK3_uc001mum.1_Missense_Mutation_p.S573R|HIPK3_uc009yjv.1_Missense_Mutation_p.S573R	NM_005734	NP_005725	Q9H422	HIPK3_HUMAN	Homo sapiens homeodomain interacting protein kinase 3 (HIPK3), transcript variant 1, mRNA.	573					anti-apoptosis|apoptosis|negative regulation of JUN kinase activity|peptidyl-serine phosphorylation|peptidyl-threonine phosphorylation|regulation of transcription, DNA-dependent|transcription, DNA-dependent	cytoplasm	ATP binding|protein serine/threonine kinase activity			endometrium(3)|kidney(3)|large_intestine(9)|liver(4)|lung(10)|ovary(2)|pancreas(1)|prostate(2)|skin(3)|stomach(1)|urinary_tract(1)	39						TTGCTTCAAGCAGTACTGCTA	0.318												
DGKZ	8525	broad.mit.edu	37	11	46393049	46393049	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr11:46393049G>A	uc001ncn.1	+	8	1344	c.1219G>A	c.(1219-1221)Gtg>Atg	p.V407M	DGKZ_uc001nch.2_Missense_Mutation_p.V235M|DGKZ_uc010rgq.2_Missense_Mutation_p.V201M|DGKZ_uc010rgr.2_Missense_Mutation_p.V223M|DGKZ_uc001ncj.2_Missense_Mutation_p.V185M|DGKZ_uc001nck.2_5'UTR|DGKZ_uc001ncm.2_Missense_Mutation_p.V218M|DGKZ_uc001ncl.2_Missense_Mutation_p.V219M|DGKZ_uc009yky.1_Missense_Mutation_p.V219M|DGKZ_uc010rgs.1_Missense_Mutation_p.V196M	NM_001105540	NP_001099010	Q13574	DGKZ_HUMAN	Homo sapiens diacylglycerol kinase, zeta (DGKZ), transcript variant 4, mRNA.	407					activation of protein kinase C activity by G-protein coupled receptor protein signaling pathway|cell migration|intracellular signal transduction|mitotic cell cycle G1/S transition DNA damage checkpoint|negative regulation of mitotic cell cycle|platelet activation	cytoplasm|lamellipodium|nucleus|plasma membrane	ATP binding|diacylglycerol kinase activity|lipid kinase activity|metal ion binding|protein binding|protein C-terminus binding			central_nervous_system(2)|endometrium(1)|kidney(2)|large_intestine(5)|lung(12)|pancreas(1)|prostate(1)|skin(1)	25				GBM - Glioblastoma multiforme(35;0.0259)|Lung(87;0.141)		CCACAGCAAGGTGTCCTGCTT	0.701												
PEX5	5830	broad.mit.edu	37	12	7343512	7343512	+	Missense_Mutation	SNP	A	A	G			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:7343512A>G	uc009zfu.2	+	3	756	c.176A>G	c.(175-177)gAa>gGa	p.E59G	PEX5_uc001qsw.3_Missense_Mutation_p.E59G|PEX5_uc010sgc.2_Missense_Mutation_p.E74G|PEX5_uc001qsu.3_Missense_Mutation_p.E59G|PEX5_uc010sgd.2_Missense_Mutation_p.E80G|PEX5_uc001qsv.3_Missense_Mutation_p.E59G	NM_001131026	NP_001124498	P50542	PEX5_HUMAN	Homo sapiens peroxisomal biogenesis factor 5 (PEX5), transcript variant 5, mRNA.	59					protein import into peroxisome matrix, translocation|protein targeting to peroxisome|protein tetramerization|protein transport	cytosol|peroxisomal matrix|peroxisomal membrane	peroxisome matrix targeting signal-1 binding|protein C-terminus binding|protein N-terminus binding			breast(1)|endometrium(3)|kidney(1)|large_intestine(5)|lung(8)|ovary(1)|prostate(1)|skin(1)	21						GTAGCTTCTGAAGATGAGGTA	0.428												
CD163	9332	broad.mit.edu	37	12	7651670	7651670	+	Missense_Mutation	SNP	T	T	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:7651670T>A	uc001qsz.3	-	3	700	c.572A>T	c.(571-573)gAt>gTt	p.D191V	CD163_uc001qta.3_Missense_Mutation_p.D191V|CD163_uc009zfw.2_Missense_Mutation_p.D191V	NM_004244	NP_004235	Q86VB7	C163A_HUMAN	Homo sapiens CD163 molecule (CD163), transcript variant 1, mRNA.	191	SRCR 2.				acute-phase response	extracellular region|integral to plasma membrane	protein binding|scavenger receptor activity			breast(1)|cervix(2)|endometrium(4)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(14)|lung(33)|ovary(6)|pancreas(2)|prostate(1)|skin(5)|urinary_tract(4)	76						AGATGCATGATCTATGTTGAA	0.428												
METTL7A	25840	broad.mit.edu	37	12	51319018	51319018	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:51319018C>T	uc001rxb.3	+	0	485	c.197C>T	c.(196-198)gCg>gTg	p.A66V	METTL7A_uc010smv.1_Missense_Mutation_p.A66V	NM_014033	NP_054752	Q9H8H3	MET7A_HUMAN	Homo sapiens methyltransferase like 7A (METTL7A), mRNA.	66						endoplasmic reticulum|lipid particle|membrane	methyltransferase activity	p.A66V(2)		endometrium(1)|large_intestine(4)|lung(4)|upper_aerodigestive_tract(1)	10						CAGGAGTTTGCGGGCCCCTCC	0.552												
TRHDE	29953	broad.mit.edu	37	12	73056901	73056901	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:73056901G>A	uc001sxa.3	+	18	3031	c.3001G>A	c.(3001-3003)Gaa>Aaa	p.E1001K		NM_013381	NP_037513	Q9UKU6	TRHDE_HUMAN	Homo sapiens thyrotropin-releasing hormone degrading enzyme (TRHDE), mRNA.	1001					cell-cell signaling|proteolysis|signal transduction	integral to plasma membrane	aminopeptidase activity|metallopeptidase activity|zinc ion binding			NS(1)|autonomic_ganglia(1)|breast(2)|endometrium(8)|kidney(3)|large_intestine(13)|lung(38)|ovary(2)|skin(4)|soft_tissue(1)|upper_aerodigestive_tract(3)|urinary_tract(3)	79						GGAAACTGTCGAAGCCAATGT	0.373												
NAP1L1	4673	broad.mit.edu	37	12	76447581	76447581	+	Missense_Mutation	SNP	A	A	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:76447581A>C	uc001sxw.2	-	8	1151	c.739T>G	c.(739-741)Ttt>Gtt	p.F247V	NAP1L1_uc001sxz.2_Missense_Mutation_p.F178V|NAP1L1_uc010stz.1_Missense_Mutation_p.F64V|NAP1L1_uc001sxx.2_Missense_Mutation_p.F247V|NAP1L1_uc010sty.1_Missense_Mutation_p.F204V|NAP1L1_uc010sua.1_Missense_Mutation_p.F247V|NAP1L1_uc001syb.3_Missense_Mutation_p.F247V	NM_139207	NP_631946	P55209	NP1L1_HUMAN	Homo sapiens nucleosome assembly protein 1-like 1 (NAP1L1), transcript variant 1, mRNA.	247					DNA replication|nucleosome assembly|positive regulation of cell proliferation	chromatin assembly complex|melanosome	protein binding			kidney(1)|large_intestine(1)|lung(3)|ovary(2)|prostate(1)|skin(1)	9		Colorectal(145;0.09)				GGTCCATCAAAAGAAAAGGGA	0.333												
CRY1	1407	broad.mit.edu	37	12	107393552	107393552	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr12:107393552C>T	uc001tmi.3	-	6	1773	c.914G>A	c.(913-915)cGc>cAc	p.R305H		NM_004075	NP_004066	Q16526	CRY1_HUMAN	Homo sapiens cryptochrome 1 (photolyase-like) (CRY1), mRNA.	305	FAD-binding.				DNA repair|protein-chromophore linkage|regulation of transcription, DNA-dependent|transcription, DNA-dependent	nucleus	blue light photoreceptor activity|DNA photolyase activity|double-stranded DNA binding|nucleotide binding|protein binding			NS(2)|breast(2)|central_nervous_system(1)|cervix(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(6)|lung(11)|ovary(3)|skin(1)	29						TTTATCAAAGCGTGGATTATT	0.433												
PCDH9	5101	broad.mit.edu	37	13	67802035	67802035	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr13:67802035C>T	uc001vik.3	-	1	1230	c.538G>A	c.(538-540)Gaa>Aaa	p.E180K	PCDH9_uc001vil.3_Missense_Mutation_p.E180K|PCDH9_uc010thl.2_Missense_Mutation_p.E180K|PCDH9_uc001vin.3_Missense_Mutation_p.E180K	NM_203487	NP_982354	Q9HC56	PCDH9_HUMAN	Homo sapiens protocadherin 9 (PCDH9), transcript variant 1, mRNA.	180	Cadherin 2.				homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			breast(2)|central_nervous_system(3)|cervix(2)|endometrium(7)|kidney(4)|large_intestine(33)|lung(30)|ovary(5)|pancreas(2)|prostate(1)|skin(4)|stomach(2)|upper_aerodigestive_tract(5)|urinary_tract(3)	103		Hepatocellular(98;0.0906)|Breast(118;0.107)		GBM - Glioblastoma multiforme(99;0.00819)		TTTAACAATTCATAATGCTGT	0.423												
FOXA1	3169	broad.mit.edu	37	14	38060635	38060635	+	Missense_Mutation	SNP	G	G	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr14:38060635G>C	uc001wuf.3	-	1	1666	c.1354C>G	c.(1354-1356)Ccc>Gcc	p.P452A	FOXA1_uc010tpz.2_Missense_Mutation_p.P419A	NM_004496	NP_004487	P55317	FOXA1_HUMAN	Homo sapiens forkhead box A1 (FOXA1), mRNA.	452					chromatin remodeling|embryo development|epithelial cell maturation involved in prostate gland development|epithelial tube branching involved in lung morphogenesis|epithelial-mesenchymal signaling involved in prostate gland development|glucose homeostasis|lung epithelial cell differentiation|negative regulation of survival gene product expression|neuron fate specification|pattern specification process|positive regulation of estrogen receptor signaling pathway|positive regulation of mitotic cell cycle|positive regulation of neuron differentiation|positive regulation of sequence-specific DNA binding transcription factor activity|prostate gland epithelium morphogenesis|prostate gland stromal morphogenesis|response to estradiol stimulus|secretory columnal luminar epithelial cell differentiation involved in prostate glandular acinus development	transcription factor complex	DNA bending activity|double-stranded DNA binding|protein domain specific binding|RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription|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|transcription regulatory region DNA binding			breast(1)|endometrium(1)|large_intestine(2)|lung(3)|prostate(12)	19	Breast(36;0.0954)|Esophageal squamous(585;0.164)|Hepatocellular(127;0.213)		Lung(238;5.41e-07)|LUAD - Lung adenocarcinoma(48;2.48e-05)|Epithelial(34;0.0454)|LUSC - Lung squamous cell carcinoma(13;0.0917)|all cancers(34;0.0925)|BRCA - Breast invasive adenocarcinoma(188;0.239)	GBM - Glioblastoma multiforme(112;0.0222)		AGGGCTGAGGGCTCGATGGGG	0.617												
LPCAT4	254531	broad.mit.edu	37	15	34653631	34653631	+	Silent	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr15:34653631C>T	uc001zig.3	-	10	1207	c.1113G>A	c.(1111-1113)acG>acA	p.T371T		NM_153613	NP_705841	Q643R3	LPCT4_HUMAN	Homo sapiens lysophosphatidylcholine acyltransferase 4 (LPCAT4), mRNA.	371					phospholipid biosynthetic process	endoplasmic reticulum membrane|integral to membrane	acyltransferase activity|calcium ion binding			NS(1)|breast(1)|large_intestine(2)|lung(5)|prostate(1)	10						CACCAGCCACCGTCTGAGGAT	0.587												
ITGA11	22801	broad.mit.edu	37	15	68612685	68612685	+	Silent	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr15:68612685G>A	uc010bib.3	-	19	2541	c.2454C>T	c.(2452-2454)tcC>tcT	p.S818S	ITGA11_uc002ari.3_Silent_p.S818S	NM_001004439	NP_001004439	Q9UKX5	ITA11_HUMAN	Homo sapiens integrin, alpha 11 (ITGA11), mRNA.	818					cell-matrix adhesion|integrin-mediated signaling pathway|muscle organ development	integrin complex	collagen binding|receptor activity			NS(2)|breast(1)|central_nervous_system(1)|endometrium(7)|kidney(6)|large_intestine(6)|lung(22)|pancreas(1)|prostate(1)|upper_aerodigestive_tract(3)|urinary_tract(2)	52					Tirofiban(DB00775)	GCGTGTATGCGGAGCAGTCCT	0.592												
SETD1A	9739	broad.mit.edu	37	16	30976386	30976386	+	Silent	SNP	T	T	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr16:30976386T>C	uc002ead.1	+	6	2009	c.1323T>C	c.(1321-1323)ggT>ggC	p.G441G		NM_014712	NP_055527	O15047	SET1A_HUMAN	Homo sapiens SET domain containing 1A (SETD1A), mRNA.	441	Pro-rich.				regulation of transcription, DNA-dependent|transcription, DNA-dependent	chromosome|nuclear speck|Set1C/COMPASS complex	histone-lysine N-methyltransferase activity|nucleotide binding|protein binding|RNA binding			NS(2)|breast(2)|central_nervous_system(1)|endometrium(5)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(9)|lung(21)|ovary(3)|prostate(2)|skin(4)|upper_aerodigestive_tract(4)|urinary_tract(1)	59						CAGAACCTGGTGGAGGCGGGG	0.716												
PRSS36	146547	broad.mit.edu	37	16	31159857	31159857	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr16:31159857C>T	uc002ebd.3	-	4	471	c.412G>A	c.(412-414)Gcc>Acc	p.A138T	PRSS36_uc010vff.2_5'UTR|PRSS36_uc010vfg.2_Missense_Mutation_p.A138T|PRSS36_uc010vfh.2_Missense_Mutation_p.A138T	NM_173502	NP_775773	Q5K4E3	POLS2_HUMAN	Homo sapiens protease, serine, 36 (PRSS36), mRNA.	138	Peptidase S1 1.				proteolysis	cytoplasm|proteinaceous extracellular matrix	serine-type endopeptidase activity			kidney(2)|large_intestine(4)|lung(8)|ovary(3)	17						GCCAGGTCGGCGCCCAGCTCC	0.756												
POLR2A	5430	broad.mit.edu	37	17	7399844	7399844	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr17:7399844G>A	uc002ghf.4	+	3	835	c.449G>A	c.(448-450)gGc>gAc	p.G150D	POLR2A_uc002ghe.3_Missense_Mutation_p.G150D	NM_000937	NP_000928	P24928	RPB1_HUMAN	Homo sapiens polymerase (RNA) II (DNA directed) polypeptide A, 220kDa (POLR2A), mRNA.	150					mRNA capping|nuclear mRNA splicing, via spliceosome|positive regulation of viral transcription|protein phosphorylation|regulation of transcription, DNA-dependent|transcription elongation from RNA polymerase II promoter|transcription initiation from RNA polymerase II promoter|transcription-coupled nucleotide-excision repair|viral reproduction	DNA-directed RNA polymerase II, core complex	DNA binding|DNA-directed RNA polymerase activity|metal ion binding|RNA-directed RNA polymerase activity|ubiquitin protein ligase binding			breast(3)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(8)|lung(17)|pancreas(1)|prostate(1)|skin(5)|upper_aerodigestive_tract(1)	50		Prostate(122;0.173)				CTTTGCAAGGGCAAAAACATA	0.537												
KIAA0100	9703	broad.mit.edu	37	17	26967617	26967617	+	Missense_Mutation	SNP	T	T	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr17:26967617T>C	uc002hbu.3	-	7	954	c.851A>G	c.(850-852)gAg>gGg	p.E284G	KIAA0100_uc002hbv.3_Missense_Mutation_p.E284G|KIAA0100_uc010crr.2_Missense_Mutation_p.E141G	NM_014680	NP_055495	Q14667	K0100_HUMAN	Homo sapiens KIAA0100 (KIAA0100), mRNA.	284						extracellular region				breast(3)|cervix(1)|endometrium(8)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(13)|lung(23)|ovary(2)|prostate(2)|skin(6)|stomach(2)|urinary_tract(3)	68	Lung NSC(42;0.00431)					GCTTGTGTTCTCCATCTTAAC	0.463												
TUBG1	7283	broad.mit.edu	37	17	40766544	40766544	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr17:40766544C>T	uc002ian.3	+	9	1425	c.1027C>T	c.(1027-1029)Cgc>Tgc	p.R343C		NM_001070	NP_001061	P23258	TBG1_HUMAN	Homo sapiens tubulin, gamma 1 (TUBG1), mRNA.	343					G2/M transition of mitotic cell cycle|meiotic spindle organization|protein polymerization	condensed nuclear chromosome|cytosol|gamma-tubulin complex|polar microtubule	GTP binding|GTPase activity|protein binding|structural constituent of cytoskeleton			endometrium(2)|kidney(2)|large_intestine(2)|lung(4)|ovary(1)|prostate(1)	12		Breast(137;0.00116)		BRCA - Breast invasive adenocarcinoma(366;0.129)		GATCCGGGAACGCAAGTTGGC	0.657												
TNFRSF11A	8792	broad.mit.edu	37	18	60021766	60021766	+	Silent	SNP	G	G	A	rs139968917		TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr18:60021766G>A	uc002lin.3	+	4	465	c.427_splice	c.e4+1	p.L143_splice	TNFRSF11A_uc010dpv.3_Splice_Site_p.L143_splice	NM_003839	NP_003830	Q9Y6Q6	TNR11_HUMAN	Homo sapiens tumor necrosis factor receptor superfamily, member 11a, NFKB activator (TNFRSF11A), mRNA.	143					adaptive immune response|cell-cell signaling|circadian temperature homeostasis|monocyte chemotaxis|osteoclast differentiation|positive regulation of cell proliferation|positive regulation of ERK1 and ERK2 cascade via TNFSF11-mediated signaling|positive regulation of fever generation by positive regulation of prostaglandin secretion|positive regulation of JUN kinase activity|positive regulation of NF-kappaB transcription factor activity|response to interleukin-1|response to lipopolysaccharide	external side of plasma membrane|integral to membrane	metal ion binding|tumor necrosis factor receptor activity			breast(3)|central_nervous_system(1)|cervix(1)|endometrium(2)|large_intestine(5)|lung(13)|skin(3)|upper_aerodigestive_tract(1)	29		Colorectal(73;0.188)				CCCAGCACCCGTGTACGGGTT	0.647												
MUC16	94025	broad.mit.edu	37	19	8962003	8962003	+	Silent	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:8962003G>A	uc002mkp.3	-	82	43578	c.43374C>T	c.(43372-43374)atC>atT	p.I14458I	MUC16_uc010dwi.3_Non-coding_Transcript|MUC16_uc010dwj.3_Silent_p.I1258I|MUC16_uc021uog.1_Non-coding_Transcript	NM_024690	NP_078966	Q8WXI7	MUC16_HUMAN	Homo sapiens mucin 16, cell surface associated (MUC16), mRNA.	13929	SEA 16.			Missing (in Ref. 3; AAK74120).	cell adhesion	extracellular space|extrinsic to membrane|integral to membrane|plasma membrane	protein binding			NS(9)|autonomic_ganglia(1)|breast(26)|central_nervous_system(11)|cervix(1)|endometrium(46)|haematopoietic_and_lymphoid_tissue(5)|kidney(35)|large_intestine(91)|liver(1)|lung(278)|ovary(17)|pancreas(2)|prostate(17)|skin(18)|soft_tissue(1)|stomach(8)|upper_aerodigestive_tract(16)|urinary_tract(7)	590						CTGCCAAGCCGATGAGGATGA	0.577												
LPPR2	64748	broad.mit.edu	37	19	11472001	11472001	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:11472001C>T	uc002mrf.2	+	5	801	c.425C>T	c.(424-426)aCg>aTg	p.T142M	LPPR2_uc002mre.2_Missense_Mutation_p.T167M|LPPR2_uc010dxy.2_5'UTR	NM_001170635	NP_001164106	Q96GM1	LPPR2_HUMAN	Homo sapiens lipid phosphate phosphatase-related protein type 2 (LPPR2), transcript variant 2, mRNA.	167						integral to membrane	phosphatidate phosphatase activity			NS(1)|breast(1)|kidney(1)|large_intestine(1)|lung(1)|skin(1)	6						CCCAACTACACGGCCCTGGGC	0.682												
CYP4F8	11283	broad.mit.edu	37	19	15726591	15726591	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:15726591G>A	uc002nbi.3	+	1	228	c.164G>A	c.(163-165)cGg>cAg	p.R55Q	CYP4F8_uc010xoi.1_Missense_Mutation_p.R55Q|CYP4F8_uc010xoj.2_Missense_Mutation_p.G17R	NM_007253	NP_009184	P98187	CP4F8_HUMAN	Homo sapiens cytochrome P450, family 4, subfamily F, polypeptide 8 (CYP4F8), mRNA.	55					prostaglandin metabolic process|xenobiotic metabolic process	endoplasmic reticulum membrane|integral to membrane|microsome	alkane 1-monooxygenase activity|aromatase activity|electron carrier activity|heme binding|oxygen binding|protein binding			breast(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(7)|lung(14)|skin(1)	26						CCGCAGCCCCGGAAACAGAAC	0.642												
PIK3R2	5296	broad.mit.edu	37	19	18277106	18277106	+	Frame_Shift_Del	DEL	T	T	-			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:18277106delT	uc002nia.1	+	11	2065	c.1553delT	c.(1552-1554)atgfs	p.M518fs	PIK3R2_uc002nib.1_Non-coding_Transcript|PIK3R2_uc010ebi.1_Non-coding_Transcript	NM_005027	NP_005018	O00459	P85B_HUMAN	Homo sapiens phosphoinositide-3-kinase, regulatory subunit 2 (beta) (PIK3R2), mRNA.	518					fibroblast growth factor receptor signaling pathway|insulin receptor signaling pathway|leukocyte migration|negative regulation of anti-apoptosis|nerve growth factor receptor signaling pathway|phosphatidylinositol-mediated signaling|platelet activation|regulation of small GTPase mediated signal transduction|small GTPase mediated signal transduction|T cell costimulation|T cell receptor signaling pathway	phosphatidylinositol 3-kinase complex	GTPase activator activity|phosphatidylinositol 3-kinase regulator activity|protein binding			endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(2)|lung(12)|ovary(3)|pancreas(1)|stomach(1)	24						GAGAAAGAGATGCAAAGGTGA	0.567												
KIRREL2	84063	broad.mit.edu	37	19	36351843	36351843	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:36351843G>A	uc002ocb.4	+	7	1173	c.961G>A	c.(961-963)Gtg>Atg	p.V321M	KIRREL2_uc002obz.4_Missense_Mutation_p.V321M|KIRREL2_uc002oca.4_Missense_Mutation_p.V271M|KIRREL2_uc002ocd.4_Missense_Mutation_p.V318M	NM_199180	NP_954649	Q6UWL6	KIRR2_HUMAN	Homo sapiens kin of IRRE like 2 (Drosophila) (KIRREL2), transcript variant 3, mRNA.	321	Ig-like C2-type 4.				cell adhesion	integral to membrane|plasma membrane				breast(2)|central_nervous_system(1)|endometrium(6)|large_intestine(6)|liver(2)|lung(22)|ovary(2)|skin(2)|upper_aerodigestive_tract(3)|urinary_tract(2)	48	all_lung(56;7.14e-07)|Lung NSC(56;1.12e-06)|Esophageal squamous(110;0.162)		LUSC - Lung squamous cell carcinoma(66;0.0515)			GCCGGAGCCCGTGTCCGTGGA	0.672												
SLC17A7	57030	broad.mit.edu	37	19	49934369	49934369	+	Missense_Mutation	SNP	G	G	A	rs17855709		TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr19:49934369G>A	uc002pnp.3	-	10	1464	c.1292C>T	c.(1291-1293)cCg>cTg	p.P431L	SLC17A7_uc002pno.3_Missense_Mutation_p.P93L	NM_020309	NP_064705	Q9P2U7	VGLU1_HUMAN	Homo sapiens solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 (SLC17A7), mRNA.	431			P -> R (in dbSNP:rs17855709).		glutamate secretion|neurotransmitter secretion	cell junction|clathrin sculpted glutamate transport vesicle membrane|integral to membrane|synaptic vesicle membrane|synaptosome	L-glutamate transmembrane transporter activity|sodium-dependent phosphate transmembrane transporter activity|sodium:inorganic phosphate symporter activity			autonomic_ganglia(1)|breast(1)|endometrium(2)|kidney(2)|large_intestine(8)|lung(7)|ovary(2)|pancreas(1)|skin(1)|stomach(1)	26		all_lung(116;1.62e-07)|Lung NSC(112;8.47e-07)|all_neural(266;0.0381)|Ovarian(192;0.0392)		OV - Ovarian serous cystadenocarcinoma(262;0.00153)|GBM - Glioblastoma multiforme(486;0.0245)		GGCGTAGCGCGGGGCTATGTC	0.607												
HK2	3099	broad.mit.edu	37	2	75081480	75081480	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr2:75081480C>T	uc002snd.3	+	1	2050	c.124C>T	c.(124-126)Cgg>Tgg	p.R42W		NM_000189	NP_000180	P52789	HXK2_HUMAN	Homo sapiens hexokinase 2 (HK2), mRNA.	42	Regulatory.				apoptotic mitochondrial changes|glucose transport|glycolysis|transmembrane transport	cytosol|mitochondrial outer membrane	ATP binding|glucokinase activity	p.R42Q(1)		breast(2)|central_nervous_system(1)|endometrium(3)|kidney(3)|large_intestine(5)|lung(22)|ovary(2)|prostate(1)|skin(2)|stomach(1)|urinary_tract(1)	43						GATCTCTAAGCGGTTCCGCAA	0.527												
UGGT1	56886	broad.mit.edu	37	2	128944331	128944331	+	Nonsense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr2:128944331G>A	uc002tps.3	+	38	4612	c.4434G>A	c.(4432-4434)tgG>tgA	p.W1478*	UGGT1_uc002tpr.3_Nonsense_Mutation_p.W1454*	NM_020120	NP_064505	Q9NYU2	UGGG1_HUMAN	Homo sapiens UDP-glucose glycoprotein glucosyltransferase 1 (UGGT1), transcript variant 1, mRNA.	1478	Glucosyltransferase (By similarity).				'de novo' posttranslational protein folding|post-translational protein modification|protein N-linked glycosylation via asparagine	endoplasmic reticulum lumen|ER-Golgi intermediate compartment	UDP-glucose:glycoprotein glucosyltransferase activity|unfolded protein binding			NS(1)|breast(1)|cervix(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(2)|kidney(9)|large_intestine(14)|lung(20)|ovary(1)|skin(4)|upper_aerodigestive_tract(2)|urinary_tract(1)	63						GTGAAACGTGGTGTGATGACG	0.413												
TTN	7273	broad.mit.edu	37	2	179571370	179571370	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr2:179571370C>T	uc021vsy.1	-	98	25724	c.25499G>A	c.(25498-25500)cGt>cAt	p.R8500H	TTN_uc021vsz.1_Intron|TTN_uc021vta.1_Intron|TTN_uc021vtb.1_Intron|TTN_uc002umz.1_Missense_Mutation_p.R5161H	NM_133378	NP_596869	Q8WZ42	TITIN_HUMAN	Homo sapiens titin (TTN), transcript variant N2-A, mRNA.	9427	Ig-like 67.						ATP binding|nucleic acid binding|protein serine/threonine kinase activity|protein tyrosine kinase activity			NS(24)|autonomic_ganglia(1)|breast(64)|central_nervous_system(14)|cervix(14)|endometrium(96)|haematopoietic_and_lymphoid_tissue(16)|kidney(91)|large_intestine(303)|liver(1)|lung(595)|ovary(58)|pancreas(17)|prostate(38)|skin(60)|stomach(29)|upper_aerodigestive_tract(1)|urinary_tract(26)	1448			OV - Ovarian serous cystadenocarcinoma(117;0.023)|Epithelial(96;0.0454)|all cancers(119;0.134)			GATGAAAACACGACCTCCTTG	0.443												
AQP12B	653437	broad.mit.edu	37	2	241621969	241621969	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr2:241621969C>T	uc010fzj.3	-	0	349	c.286G>A	c.(286-288)Gtg>Atg	p.V96M	AQP12B_uc002vzt.3_Intron	NM_001102467	NP_001095937	A6NM10	AQ12B_HUMAN	Homo sapiens aquaporin 12B (AQP12B), mRNA.	84						integral to membrane	transporter activity	p.V96V(1)		breast(1)|central_nervous_system(1)|cervix(1)|endometrium(1)|lung(8)|ovary(1)	13		all_epithelial(40;1.71e-15)|Breast(86;2.14e-05)|Renal(207;0.00183)|Ovarian(221;0.0228)|all_lung(227;0.0294)|all_neural(83;0.0459)|Lung NSC(271;0.094)|all_hematologic(139;0.158)|Melanoma(123;0.16)|Hepatocellular(293;0.244)		Epithelial(32;2.2e-31)|all cancers(36;1.08e-28)|OV - Ovarian serous cystadenocarcinoma(60;2.13e-15)|Kidney(56;3.04e-09)|KIRC - Kidney renal clear cell carcinoma(57;3.23e-08)|BRCA - Breast invasive adenocarcinoma(100;7.52e-06)|Lung(119;0.00163)|LUSC - Lung squamous cell carcinoma(224;0.008)|Colorectal(34;0.0124)|COAD - Colon adenocarcinoma(134;0.0757)		TGCAGGGACACGGTGGGGTTG	0.687												
SULF2	55959	broad.mit.edu	37	20	46386007	46386007	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr20:46386007C>T	uc002xto.3	-	1	431	c.101G>A	c.(100-102)aGg>aAg	p.R34K	SULF2_uc002xtr.3_Missense_Mutation_p.R34K|SULF2_uc002xtq.3_Missense_Mutation_p.R34K|SULF2_uc010ghv.1_Missense_Mutation_p.R34K	NM_018837	NP_061325	Q8IWU5	SULF2_HUMAN	Homo sapiens sulfatase 2 (SULF2), transcript variant 1, mRNA.	34					bone development|heparan sulfate proteoglycan metabolic process|kidney development|negative regulation of fibroblast growth factor receptor signaling pathway	cell surface|endoplasmic reticulum|extracellular space|Golgi stack	arylsulfatase activity|calcium ion binding			breast(2)|endometrium(4)|kidney(1)|large_intestine(7)|lung(22)|ovary(4)|pancreas(1)|prostate(5)|skin(5)|upper_aerodigestive_tract(2)|urinary_tract(1)	54						CCTCTGAAACCTGCCTTTCAG	0.647												
SLCO4A1	28231	broad.mit.edu	37	20	61291766	61291766	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr20:61291766C>T	uc002ydb.1	+	3	1095	c.890C>T	c.(889-891)aCg>aTg	p.T297M		NM_016354	NP_057438	Q96BD0	SO4A1_HUMAN	Homo sapiens solute carrier organic anion transporter family, member 4A1 (SLCO4A1), mRNA.	297					sodium-independent organic anion transport	integral to membrane|plasma membrane	thyroid hormone transmembrane transporter activity	p.T297M(2)		endometrium(6)|kidney(2)|large_intestine(1)|lung(7)|ovary(3)|prostate(2)	21	Breast(26;3.65e-08)		BRCA - Breast invasive adenocarcinoma(19;2.33e-06)			TTCCACAGGACGGAGCTGACC	0.687												
KRTAP10-5	386680	broad.mit.edu	37	21	46000294	46000294	+	Silent	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr21:46000294C>T	uc002zfl.1	-	0	188	c.162G>A	c.(160-162)gcG>gcA	p.A54A	TSPEAR_uc002zfe.1_Intron|TSPEAR_uc010gpv.1_Intron	NM_198694	NP_941967	P60370	KR105_HUMAN	Homo sapiens keratin associated protein 10-5 (KRTAP10-5), mRNA.	54	22 X 5 AA repeats of C-C-X(3).					keratin filament				endometrium(2)|kidney(1)|lung(9)|prostate(1)|upper_aerodigestive_tract(1)	14						GCTCACAGGCCGCCTGGCAGC	0.716												
C1QTNF6	114904	broad.mit.edu	37	22	37581311	37581311	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr22:37581311C>T	uc003aqx.1	-	1	499	c.236G>A	c.(235-237)cGc>cAc	p.R79H	C1QTNF6_uc003aqw.1_Missense_Mutation_p.R60H|C1QTNF6_uc003aqy.1_Missense_Mutation_p.R79H|C1QTNF6_uc003aqz.1_Non-coding_Transcript	NM_182486	NP_872292	Q9BXI9	C1QT6_HUMAN	Homo sapiens C1q and tumor necrosis factor related protein 6 (C1QTNF6), transcript variant 2, mRNA.	60	Collagen-like.					collagen		p.G78C(1)		breast(1)|large_intestine(2)|lung(6)|stomach(1)|upper_aerodigestive_tract(1)	11						GGCGTGGGGGCGGCCGGAGGA	0.632												
DCLK3	85443	broad.mit.edu	37	3	36779774	36779774	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr3:36779774C>T	uc003cgi.2	-	1	868	c.377G>A	c.(376-378)gGg>gAg	p.G126E		NM_033403	NP_208382	Q9C098	DCLK3_HUMAN	Homo sapiens doublecortin-like kinase 3 (DCLK3), mRNA.	126						cytoplasm|nucleus	ATP binding|protein serine/threonine kinase activity	p.G126E(2)		breast(3)|endometrium(3)|kidney(2)|large_intestine(11)|lung(20)|ovary(2)|pancreas(1)|prostate(1)|skin(2)|stomach(1)|upper_aerodigestive_tract(2)	48						AATCTCCACCCCAAGATGCTT	0.567												
SLC6A20	54716	broad.mit.edu	37	3	45801400	45801400	+	Silent	SNP	G	G	A	rs143985135		TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr3:45801400G>A	uc011bai.2	-	9	1702	c.1578C>T	c.(1576-1578)agC>agT	p.S526S	SLC6A20_uc003cow.3_Silent_p.S176S|SLC6A20_uc011baj.2_Silent_p.S489S	NM_020208	NP_064593	Q9NP91	S6A20_HUMAN	Homo sapiens solute carrier family 6 (proline IMINO transporter), member 20 (SLC6A20), transcript variant 1, mRNA.	526					cellular nitrogen compound metabolic process|glycine transport|proline transport	apical plasma membrane|integral to plasma membrane	amino acid transmembrane transporter activity|neurotransmitter:sodium symporter activity	p.S526S(1)|p.S489S(1)		breast(1)|endometrium(1)|large_intestine(6)|ovary(2)|skin(2)|urinary_tract(1)	13				BRCA - Breast invasive adenocarcinoma(193;0.01)|KIRC - Kidney renal clear cell carcinoma(197;0.0225)|Kidney(197;0.0267)		GGATGTAGTCGCTCAGGTAGA	0.592												
NIT2	56954	broad.mit.edu	37	3	100057936	100057936	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr3:100057936C>T	uc003dtv.3	+	1	87	c.13C>T	c.(13-15)Cgc>Tgc	p.R5C	NIT2_uc011bha.1_Missense_Mutation_p.R5C	NM_020202	NP_064587	Q9NQR4	NIT2_HUMAN	Homo sapiens nitrilase family, member 2 (NIT2), mRNA.	5	CN hydrolase.				nitrogen compound metabolic process		omega-amidase activity			breast(1)|endometrium(1)|kidney(4)|large_intestine(3)|lung(4)|ovary(1)|prostate(2)|skin(1)	17						CTCAGCTTTCCGCTTGGCCCT	0.473												
DLG1	1739	broad.mit.edu	37	3	196921382	196921382	+	Missense_Mutation	SNP	C	C	G			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr3:196921382C>G	uc010ial.3	-	4	656	c.397G>C	c.(397-399)Gaa>Caa	p.E133Q	DLG1_uc011bud.2_5'UTR|DLG1_uc003fxo.4_Missense_Mutation_p.E133Q|DLG1_uc003fxn.4_Missense_Mutation_p.E133Q|DLG1_uc011bue.2_Missense_Mutation_p.E133Q|DLG1_uc011buf.1_Non-coding_Transcript|DLG1_uc003fxp.2_Non-coding_Transcript|DLG1_uc010iam.1_Missense_Mutation_p.E133Q	NM_001098424	NP_001091894	Q12959	DLG1_HUMAN	Homo sapiens discs, large homolog 1 (Drosophila) (DLG1), transcript variant 1, mRNA.	133					actin filament organization|axon guidance|cell-cell adhesion|cortical actin cytoskeleton organization|endothelial cell proliferation|establishment or maintenance of cell polarity|interspecies interaction between organisms|mitotic cell cycle G1/S transition checkpoint|negative regulation of mitotic cell cycle|protein localization in plasma membrane|synaptic transmission|tight junction assembly	basolateral plasma membrane|cytosol|endoplasmic reticulum membrane|immunological synapse|MPP7-DLG1-LIN7 complex|nucleus|postsynaptic density|postsynaptic membrane|sarcolemma|tight junction	cytoskeletal protein binding|guanylate kinase activity|L27 domain binding|phosphatase binding|phosphoprotein phosphatase activity|potassium channel regulator activity|protein binding|protein C-terminus binding|protein kinase binding			breast(2)|endometrium(1)|kidney(3)|large_intestine(4)|liver(1)|lung(9)|ovary(3)|prostate(1)|skin(1)|urinary_tract(1)	26	all_cancers(143;6.22e-10)|Ovarian(172;0.0418)|Breast(254;0.0589)	Lung NSC(153;0.133)	Epithelial(36;3.23e-24)|all cancers(36;2.15e-22)|OV - Ovarian serous cystadenocarcinoma(49;3.88e-19)|LUSC - Lung squamous cell carcinoma(58;1.51e-06)|Lung(62;1.95e-06)	GBM - Glioblastoma multiforme(46;0.0148)		TGAACCAATTCTGGACCTATC	0.353												
SLIT2	9353	broad.mit.edu	37	4	20543202	20543202	+	Silent	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr4:20543202C>T	uc003gpr.1	+	19	2307	c.2103C>T	c.(2101-2103)ccC>ccT	p.P701P	SLIT2_uc003gps.1_Silent_p.P693P	NM_004787	NP_004778	O94813	SLIT2_HUMAN	Homo sapiens slit homolog 2 (Drosophila) (SLIT2), mRNA.	701	LRRCT 3.				apoptosis involved in luteolysis|axon extension involved in axon guidance|branching morphogenesis of a tube|cell migration involved in sprouting angiogenesis|cellular response to heparin|cellular response to hormone stimulus|chemorepulsion involved in postnatal olfactory bulb interneuron migration|corticospinal neuron axon guidance through spinal cord|induction of negative chemotaxis|motor axon guidance|negative regulation of actin filament polymerization|negative regulation of cell growth|negative regulation of cellular response to growth factor stimulus|negative regulation of chemokine-mediated signaling pathway|negative regulation of endothelial cell migration|negative regulation of lamellipodium assembly|negative regulation of mononuclear cell migration|negative regulation of neutrophil chemotaxis|negative regulation of protein phosphorylation|negative regulation of retinal ganglion cell axon guidance|negative regulation of small GTPase mediated signal transduction|negative regulation of smooth muscle cell chemotaxis|negative regulation of vascular permeability|positive regulation of apoptosis|positive regulation of axonogenesis|response to cortisol stimulus|retinal ganglion cell axon guidance|Roundabout signaling pathway|ureteric bud development	cell surface|cytoplasm|extracellular space|plasma membrane	calcium ion binding|GTPase inhibitor activity|heparin binding|laminin-1 binding|protein homodimerization activity|proteoglycan binding|Roundabout binding			NS(1)|breast(4)|central_nervous_system(4)|cervix(1)|endometrium(5)|kidney(7)|large_intestine(17)|lung(60)|ovary(3)|pancreas(1)|prostate(2)|skin(10)|upper_aerodigestive_tract(1)	116						AAGAAATACCCATCCAGGATG	0.443												
N4BP2	55728	broad.mit.edu	37	4	40119548	40119548	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr4:40119548G>A	uc003guy.4	+	7	2062	c.1724G>A	c.(1723-1725)cGt>cAt	p.R575H	N4BP2_uc010ifq.3_Missense_Mutation_p.R495H|N4BP2_uc010ifr.3_Missense_Mutation_p.R495H	NM_018177	NP_060647	Q86UW6	N4BP2_HUMAN	Homo sapiens NEDD4 binding protein 2 (N4BP2), mRNA.	575						cytoplasm	ATP binding|ATP-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity|endonuclease activity|protein binding			breast(4)|endometrium(3)|kidney(12)|large_intestine(7)|liver(2)|lung(22)|ovary(1)|pancreas(1)|prostate(2)|skin(5)|upper_aerodigestive_tract(1)	60						CATTATCAACGTTTTGTTTCA	0.363												
PCDH10	57575	broad.mit.edu	37	4	134084209	134084209	+	Missense_Mutation	SNP	G	G	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr4:134084209G>T	uc003iha.3	+	3	3701	c.2875G>T	c.(2875-2877)Gtc>Ttc	p.V959F		NM_032961	NP_116586	Q9P2E7	PCD10_HUMAN	Homo sapiens protocadherin 10 (PCDH10), transcript variant 1, mRNA.	959					homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			NS(2)|breast(1)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(6)|large_intestine(30)|liver(1)|lung(72)|ovary(2)|prostate(2)|skin(2)|stomach(1)|upper_aerodigestive_tract(6)|urinary_tract(2)	136				LUSC - Lung squamous cell carcinoma(193;0.227)		GCCTTCTTTTGTCCCTTCTGA	0.488												
DCLK2	166614	broad.mit.edu	37	4	151170830	151170830	+	Silent	SNP	C	C	G			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr4:151170830C>G	uc003ilo.4	+	15	2872	c.2118C>G	c.(2116-2118)gtC>gtG	p.V706V	DCLK2_uc003ilp.4_Non-coding_Transcript|DCLK2_uc003ilm.4_Silent_p.V689V|DCLK2_uc003iln.4_Silent_p.V688V	NM_001040261	NP_001035351	Q8N568	DCLK2_HUMAN	Homo sapiens doublecortin-like kinase 2 (DCLK2), transcript variant 2, mRNA.	689					intracellular signal transduction	cytoplasm|cytoskeleton	ATP binding|protein serine/threonine kinase activity			breast(1)|endometrium(4)|kidney(1)|large_intestine(7)|lung(7)|ovary(3)|pancreas(1)|prostate(1)|skin(1)	26	all_hematologic(180;0.151)					GGGTCTCCGTCATCATGGTGA	0.532												
AP3S1	1176	broad.mit.edu	37	5	115177778	115177778	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr5:115177778G>A	uc003krl.3	+	0	160	c.44G>A	c.(43-45)cGg>cAg	p.R15Q	AP3S1_uc003krk.3_5'UTR|ATG12_uc021ycr.1_5'Flank|ATG12_uc021ycs.1_5'Flank|ATG12_uc003krh.3_5'Flank|ATG12_uc003kri.3_5'Flank	NM_001284	NP_001275	Q92572	AP3S1_HUMAN	Homo sapiens adaptor-related protein complex 3, sigma 1 subunit (AP3S1), mRNA.	15					insulin receptor signaling pathway|intracellular protein transport|vesicle-mediated transport	AP-type membrane coat adaptor complex|cytoplasmic vesicle membrane|Golgi apparatus|transport vesicle	protein binding|protein transporter activity			cervix(1)|endometrium(2)|kidney(1)|large_intestine(3)|lung(2)|ovary(1)|pancreas(1)|prostate(1)	12		all_cancers(142;0.00377)|all_epithelial(76;0.000129)|Prostate(80;0.0132)|Ovarian(225;0.0776)|Lung NSC(810;0.245)		OV - Ovarian serous cystadenocarcinoma(64;1.08e-07)|Epithelial(69;1.11e-06)|all cancers(49;5.2e-05)		GGGAAGCCGCGGCTCTCCAAG	0.692												
DOCK2	1794	broad.mit.edu	37	5	169506008	169506008	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr5:169506008C>T	uc003maf.3	+	48	5104	c.5024C>T	c.(5023-5025)aCg>aTg	p.T1675M	DOCK2_uc011der.2_Non-coding_Transcript|DOCK2_uc010jjm.3_Missense_Mutation_p.T1167M|DOCK2_uc003mah.3_Missense_Mutation_p.T231M	NM_004946	NP_004937	Q92608	DOCK2_HUMAN	Homo sapiens dedicator of cytokinesis 2 (DOCK2), mRNA.	1675					actin cytoskeleton organization|regulation of defense response to virus by virus|viral reproduction	cytoskeleton|cytosol|endomembrane system|membrane	electron carrier activity|GTP binding|GTPase binding|heme binding|Rac guanyl-nucleotide exchange factor activity|T cell receptor binding			NS(2)|breast(5)|cervix(1)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(9)|large_intestine(42)|liver(2)|lung(63)|ovary(5)|pancreas(3)|prostate(7)|skin(5)|stomach(2)|upper_aerodigestive_tract(3)	160	Renal(175;0.000159)|Lung NSC(126;0.0221)|all_lung(126;0.0337)	Medulloblastoma(196;0.0399)|all_neural(177;0.0966)	Kidney(164;7.53e-05)|KIRC - Kidney renal clear cell carcinoma(164;0.000525)			TCACCCAAGACGCCGAGAGTG	0.557												
ICK	22858	broad.mit.edu	37	6	52883129	52883129	+	Frame_Shift_Del	DEL	T	T	-			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr6:52883129delT	uc003pbh.2	-	8	1153	c.663_splice	c.e8+1	p.K221_splice	ICK_uc003pbi.2_Splice_Site_p.K221_splice|ICK_uc003pbj.3_Splice_Site_p.K221_splice	NM_016513	NP_057597	Q9UPZ9	ICK_HUMAN	Homo sapiens intestinal cell (MAK-like) kinase (ICK), transcript variant 2, mRNA.	221	Protein kinase.				intracellular protein kinase cascade|multicellular organismal development	cytosol|nucleus	ATP binding|cyclin-dependent protein kinase activity|magnesium ion binding			breast(1)|central_nervous_system(2)|endometrium(4)|kidney(2)|large_intestine(6)|lung(10)|ovary(1)|prostate(1)|skin(3)|stomach(1)	31	Lung NSC(77;0.103)					TATCATTACCTTTTTTGGTGT	0.502												
WDR27	253769	broad.mit.edu	37	6	170036474	170036474	+	Missense_Mutation	SNP	T	T	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr6:170036474T>C	uc003qwx.3	-	18	2516	c.1996A>G	c.(1996-1998)Att>Gtt	p.I666V	WDR27_uc003qwv.2_Intron|WDR27_uc021zio.1_Missense_Mutation_p.I666V|WDR27_uc003qwy.3_Missense_Mutation_p.I539V	NM_182552	NP_872358	A2RRH5	WDR27_HUMAN	Homo sapiens WD repeat domain 27 (WDR27), transcript variant 1, mRNA.	636										endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(2)|lung(5)|pancreas(1)|skin(1)	12		Breast(66;1.53e-05)|Ovarian(120;0.216)		OV - Ovarian serous cystadenocarcinoma(33;6.48e-20)|BRCA - Breast invasive adenocarcinoma(81;3.56e-07)|GBM - Glioblastoma multiforme(31;0.00168)		TACCTCTTAATCTCATCTTTG	0.378												
FAM126A	84668	broad.mit.edu	37	7	23023600	23023600	+	Nonsense_Mutation	SNP	G	G	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr7:23023600G>T	uc003svm.4	-	2	371	c.116C>A	c.(115-117)tCa>tAa	p.S39*	FAM126A_uc003svn.4_5'UTR|FAM126A_uc011jyr.1_Intron	NM_032581	NP_115970	Q9BYI3	HYCCI_HUMAN	Homo sapiens family with sequence similarity 126, member A (FAM126A), mRNA.	39						cytoplasm|membrane	signal transducer activity			breast(2)|central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(7)|lung(8)|urinary_tract(2)	23						ATAGAGAGATGAAACTAAAGA	0.269												
MUC17	140453	broad.mit.edu	37	7	100683180	100683180	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr7:100683180G>A	uc003uxp.1	+	2	8536	c.8483G>A	c.(8482-8484)gGc>gAc	p.G2828D	MUC17_uc010lho.1_Non-coding_Transcript	NM_001040105	NP_001035194	Q685J3	MUC17_HUMAN	Homo sapiens mucin 17, cell surface associated (MUC17), mRNA.	2828	59 X approximate tandem repeats.|Ser-rich.					extracellular region|integral to membrane|plasma membrane	extracellular matrix constituent, lubricant activity			NS(3)|breast(14)|central_nervous_system(2)|cervix(2)|endometrium(27)|haematopoietic_and_lymphoid_tissue(2)|kidney(18)|large_intestine(28)|lung(179)|ovary(19)|pancreas(1)|prostate(13)|skin(26)|stomach(2)|upper_aerodigestive_tract(3)|urinary_tract(4)	343	Lung NSC(181;0.136)|all_lung(186;0.182)					TCTGAGGCTGGCACCCTTTCA	0.498												
ARFGEF1	10565	broad.mit.edu	37	8	68140317	68140317	+	Missense_Mutation	SNP	T	T	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr8:68140317T>C	uc003xxo.2	-	24	3862	c.3472A>G	c.(3472-3474)Acg>Gcg	p.T1158A	ARFGEF1_uc003xxl.1_Missense_Mutation_p.T612A|ARFGEF1_uc003xxn.2_Missense_Mutation_p.T141A	NM_006421	NP_006412	Q9Y6D6	BIG1_HUMAN	Homo sapiens ADP-ribosylation factor guanine nucleotide-exchange factor 1 (brefeldin A-inhibited) (ARFGEF1), mRNA.	1158					exocytosis|regulation of ARF protein signal transduction	cytoplasm	ARF guanyl-nucleotide exchange factor activity|myosin binding			breast(1)|endometrium(14)|kidney(4)|large_intestine(17)|lung(20)|ovary(4)|skin(1)|stomach(1)|upper_aerodigestive_tract(2)|urinary_tract(1)	65	Breast(64;0.214)	Lung NSC(129;0.0908)|all_lung(136;0.152)	Epithelial(68;0.0043)|OV - Ovarian serous cystadenocarcinoma(28;0.00578)|all cancers(69;0.0173)|BRCA - Breast invasive adenocarcinoma(89;0.206)			GGGTGTGTCGTGGAAAGTAAT	0.318												
SLC39A4	55630	broad.mit.edu	37	8	145642115	145642115	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr8:145642115G>A	uc003zcq.3	-	0	159	c.59C>T	c.(58-60)gCg>gTg	p.A20V	SLC39A4_uc003zco.3_5'Flank|SLC39A4_uc003zcp.3_5'Flank	NM_130849	NP_570901	Q6P5W5	S39A4_HUMAN	Homo sapiens solute carrier family 39 (zinc transporter), member 4 (SLC39A4), transcript variant 2, mRNA.	20						cytoplasmic membrane-bounded vesicle|integral to membrane|recycling endosome membrane	zinc ion transmembrane transporter activity			endometrium(1)|kidney(1)|large_intestine(1)|lung(5)|ovary(1)|prostate(2)|skin(1)|upper_aerodigestive_tract(2)	14	all_cancers(97;6.64e-12)|all_epithelial(106;2.89e-10)|Lung NSC(106;5.7e-05)|all_lung(105;0.000174)|Ovarian(258;0.0173)|Acute lymphoblastic leukemia(118;0.155)		OV - Ovarian serous cystadenocarcinoma(54;1.08e-41)|Epithelial(56;1.12e-40)|all cancers(56;8.17e-36)|BRCA - Breast invasive adenocarcinoma(115;0.0407)|Colorectal(110;0.055)			GGACGCCGTCGCCGTCACCAC	0.662												
WASH1	375690	broad.mit.edu	37	9	17147	17147	+	Missense_Mutation	SNP	T	T	C			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr9:17147T>C	uc010mgm.1	-	6	844	c.701A>G	c.(700-702)tAt>tGt	p.Y234C	WASH1_uc022bcs.1_Non-coding_Transcript|WASH1_uc011llq.1_Non-coding_Transcript|WASH1_uc003zfu.1_Missense_Mutation_p.Y247C	NM_182905	NP_878908	A8K0Z3	WASH1_HUMAN	Homo sapiens WAS protein family homolog 1 (WASH1), mRNA.	234					Arp2/3 complex-mediated actin nucleation|retrograde transport, endosome to Golgi	early endosome membrane|recycling endosome membrane|WASH complex	actin binding|alpha-tubulin binding					all_lung(41;0.218)	all_cancers(5;3.04e-16)|all_epithelial(5;4.68e-12)|all_lung(10;1.94e-10)|Lung NSC(10;3.61e-10)|Acute lymphoblastic leukemia(5;0.00439)|Breast(48;0.0148)|all_hematologic(5;0.024)|Prostate(43;0.122)	Kidney(42;0.112)|KIRC - Kidney renal clear cell carcinoma(5;0.157)	all cancers(5;0.000704)|Lung(218;0.00755)|GBM - Glioblastoma multiforme(5;0.0149)|Epithelial(6;0.0154)		GTCTGGCACATAGAAGTAGTT	0.587												
PAPPA	5069	broad.mit.edu	37	9	118997909	118997909	+	Missense_Mutation	SNP	G	G	A			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr9:118997909G>A	uc004bjn.3	+	6	3106	c.2725G>A	c.(2725-2727)Gta>Ata	p.V909I	PAPPA_uc011lxp.1_Missense_Mutation_p.V604I|PAPPA_uc011lxq.2_Intron	NM_002581	NP_002572	Q13219	PAPP1_HUMAN	Homo sapiens pregnancy-associated plasma protein A, pappalysin 1 (PAPPA), mRNA.	909					cell differentiation|female pregnancy	cytoplasm|extracellular region|membrane	metalloendopeptidase activity|zinc ion binding			NS(1)|breast(4)|endometrium(9)|kidney(2)|large_intestine(23)|lung(33)|ovary(4)|pancreas(2)|prostate(5)|skin(7)|stomach(1)|upper_aerodigestive_tract(6)|urinary_tract(1)	98						TAGGAAATTCGTAGACATGTA	0.517												
LAMC3	10319	broad.mit.edu	37	9	133907535	133907535	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chr9:133907535C>T	uc004caa.1	+	2	880	c.782C>T	c.(781-783)gCc>gTc	p.A261V		NM_006059	NP_006050	Q9Y6N6	LAMC3_HUMAN	Homo sapiens laminin, gamma 3 (LAMC3), mRNA.	261	Laminin N-terminal.				cell adhesion	basement membrane|membrane	structural molecule activity			endometrium(6)|haematopoietic_and_lymphoid_tissue(1)|kidney(7)|large_intestine(12)|lung(31)|ovary(3)|pancreas(1)|prostate(3)|upper_aerodigestive_tract(2)|urinary_tract(3)	69	all_hematologic(7;0.0028)	Myeloproliferative disorder(178;0.204)		OV - Ovarian serous cystadenocarcinoma(145;5.06e-05)|Epithelial(140;0.000551)		TACTATTATGCCGTGTCCGAC	0.612												
GABRQ	55879	broad.mit.edu	37	X	151820044	151820044	+	Silent	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chrX:151820044C>T	uc004ffp.1	+	7	977	c.957C>T	c.(955-957)ctC>ctT	p.L319L		NM_018558	NP_061028	Q9UN88	GBRT_HUMAN	Homo sapiens gamma-aminobutyric acid (GABA) receptor, theta (GABRQ), mRNA.	319						cell junction|chloride channel complex|integral to plasma membrane|postsynaptic membrane	chloride channel activity|extracellular ligand-gated ion channel activity|GABA-A receptor activity|neurotransmitter transporter activity			breast(1)|central_nervous_system(1)|endometrium(1)|kidney(4)|large_intestine(9)|lung(25)|ovary(3)|pancreas(2)|prostate(2)|skin(3)|upper_aerodigestive_tract(1)	52	Acute lymphoblastic leukemia(192;6.56e-05)					GGGATAAGCTCCCCAACATTT	0.448												
PCDH11Y	83259	broad.mit.edu	37	Y	5605715	5605715	+	Missense_Mutation	SNP	C	C	T			TCGA-27-2523-01A-01D-1494-08	TCGA-27-2523-10A-01D-1494-08								Untested	Somatic	Phase_I	WXS	none			Illumina GAIIx	d60f54f5-b154-42c4-99fb-cea4e7a33dc7	28ea912e-e998-458c-879e-38d55938a2fb	g.chrY:5605715C>T	uc004fqo.3	+	4	4489	c.3755C>T	c.(3754-3756)tCt>tTt	p.S1252F	PCDH11Y_uc022ciy.1_Non-coding_Transcript	NM_032973	NP_116755	Q9BZA8	PC11Y_HUMAN	Homo sapiens protocadherin 11 Y-linked (PCDH11Y), transcript variant c, mRNA.	1252					homophilic cell adhesion	integral to membrane|plasma membrane	calcium ion binding			autonomic_ganglia(1)|kidney(2)|large_intestine(7)|lung(14)|prostate(1)|skin(1)|upper_aerodigestive_tract(1)	27						AGCCACAGCTCTTCTCTGCCA	0.552												
