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	X1000Genome_AA	X1000Genome_AC	X1000Genome_AF	X1000Genome_AFR_AF	X1000Genome_AMR_AF	X1000Genome_AN	X1000Genome_ASN_AF	X1000Genome_AVGPOST	X1000Genome_CIEND	X1000Genome_CIPOS	X1000Genome_END	X1000Genome_ERATE	X1000Genome_EUR_AF	X1000Genome_HOMLEN	X1000Genome_HOMSEQ	X1000Genome_LDAF	X1000Genome_RSQ	X1000Genome_SNPSOURCE	X1000Genome_SVLEN	X1000Genome_SVTYPE	X1000Genome_THETA	X1000Genome_VT	ACHILLES_Lineage_Results_Top_Genes	CGC_Cancer.Germline.Mut	CGC_Cancer.Molecular.Genetics	CGC_Cancer.Somatic.Mut	CGC_Cancer.Syndrome	CGC_Chr	CGC_Chr.Band	CGC_GeneID	CGC_Name	CGC_Other.Germline.Mut	CGC_Tissue.Type	COSMIC_n_overlapping_mutations	COSMIC_overlapping_mutation_descriptions	COSMIC_overlapping_primary_sites	ClinVar_ASSEMBLY	ClinVar_HGMD_ID	ClinVar_SYM	ClinVar_TYPE	ClinVar_rs	ESP_AA	ESP_AAC	ESP_AA_AC	ESP_AA_AGE	ESP_AA_GTC	ESP_AvgAAsampleReadDepth	ESP_AvgEAsampleReadDepth	ESP_AvgSampleReadDepth	ESP_CA	ESP_CDP	ESP_CG	ESP_CP	ESP_Chromosome	ESP_DBSNP	ESP_DP	ESP_EA_AC	ESP_EA_AGE	ESP_EA_GTC	ESP_EXOME_CHIP	ESP_FG	ESP_GL	ESP_GM	ESP_GS	ESP_GTC	ESP_GTS	ESP_GWAS_PUBMED	ESP_MAF	ESP_PH	ESP_PP	ESP_Position	ESP_TAC	ESP_TotalAAsamplesCovered	ESP_TotalEAsamplesCovered	ESP_TotalSamplesCovered	Ensembl_so_accession	Ensembl_so_term	Familial_Cancer_Genes_Reference	Familial_Cancer_Genes_Synonym	HGNC_Accession.Numbers	HGNC_CCDS.IDs	HGNC_Chromosome	HGNC_Date.Modified	HGNC_Date.Name.Changed	HGNC_Date.Symbol.Changed	HGNC_Ensembl.Gene.ID	HGNC_Ensembl.ID.supplied.by.Ensembl.	HGNC_Entrez.Gene.ID	HGNC_Entrez.Gene.ID.supplied.by.NCBI.	HGNC_Enzyme.IDs	HGNC_Gene.family.description	HGNC_HGNC.ID	HGNC_Locus.Group	HGNC_Locus.Type	HGNC_Name.Synonyms	HGNC_OMIM.ID.supplied.by.NCBI.	HGNC_Previous.Names	HGNC_Previous.Symbols	HGNC_Primary.IDs	HGNC_Pubmed.IDs	HGNC_Record.Type	HGNC_RefSeq.IDs	HGNC_RefSeq.supplied.by.NCBI.	HGNC_Secondary.IDs	HGNC_Status	HGNC_Synonyms	HGNC_UCSC.ID.supplied.by.UCSC.	HGNC_UniProt.ID.supplied.by.UniProt.	HGNC_VEGA.IDs	HGVS_coding_DNA_change	HGVS_genomic_change	HGVS_protein_change	ORegAnno_bin	UniProt_alt_uniprot_accessions	build	ccds_id	dbNSFP_1000Gp1_AC	dbNSFP_1000Gp1_AF	dbNSFP_1000Gp1_AFR_AC	dbNSFP_1000Gp1_AFR_AF	dbNSFP_1000Gp1_AMR_AC	dbNSFP_1000Gp1_AMR_AF	dbNSFP_1000Gp1_ASN_AC	dbNSFP_1000Gp1_ASN_AF	dbNSFP_1000Gp1_EUR_AC	dbNSFP_1000Gp1_EUR_AF	dbNSFP_Ancestral_allele	dbNSFP_CADD_phred	dbNSFP_CADD_raw	dbNSFP_CADD_raw_rankscore	dbNSFP_ESP6500_AA_AF	dbNSFP_ESP6500_EA_AF	dbNSFP_Ensembl_geneid	dbNSFP_Ensembl_transcriptid	dbNSFP_FATHMM_pred	dbNSFP_FATHMM_rankscore	dbNSFP_FATHMM_score	dbNSFP_GERP.._NR	dbNSFP_GERP.._RS	dbNSFP_GERP.._RS_rankscore	dbNSFP_Interpro_domain	dbNSFP_LRT_Omega	dbNSFP_LRT_converted_rankscore	dbNSFP_LRT_pred	dbNSFP_LRT_score	dbNSFP_LR_pred	dbNSFP_LR_rankscore	dbNSFP_LR_score	dbNSFP_MutationAssessor_pred	dbNSFP_MutationAssessor_rankscore	dbNSFP_MutationAssessor_score	dbNSFP_MutationTaster_converted_rankscore	dbNSFP_MutationTaster_pred	dbNSFP_MutationTaster_score	dbNSFP_Polyphen2_HDIV_pred	dbNSFP_Polyphen2_HDIV_rankscore	dbNSFP_Polyphen2_HDIV_score	dbNSFP_Polyphen2_HVAR_pred	dbNSFP_Polyphen2_HVAR_rankscore	dbNSFP_Polyphen2_HVAR_score	dbNSFP_RadialSVM_pred	dbNSFP_RadialSVM_rankscore	dbNSFP_RadialSVM_score	dbNSFP_Reliability_index	dbNSFP_SIFT_converted_rankscore	dbNSFP_SIFT_pred	dbNSFP_SIFT_score	dbNSFP_SLR_test_statistic	dbNSFP_SiPhy_29way_logOdds	dbNSFP_SiPhy_29way_logOdds_rankscore	dbNSFP_SiPhy_29way_pi	dbNSFP_UniSNP_ids	dbNSFP_Uniprot_aapos	dbNSFP_Uniprot_acc	dbNSFP_Uniprot_id	dbNSFP_aaalt	dbNSFP_aapos	dbNSFP_aapos_FATHMM	dbNSFP_aapos_SIFT	dbNSFP_aaref	dbNSFP_cds_strand	dbNSFP_codonpos	dbNSFP_fold.degenerate	dbNSFP_genename	dbNSFP_hg18_pos.1.coor.	dbNSFP_phastCons100way_vertebrate	dbNSFP_phastCons100way_vertebrate_rankscore	dbNSFP_phastCons46way_placental	dbNSFP_phastCons46way_placental_rankscore	dbNSFP_phastCons46way_primate	dbNSFP_phastCons46way_primate_rankscore	dbNSFP_phyloP100way_vertebrate	dbNSFP_phyloP100way_vertebrate_rankscore	dbNSFP_phyloP46way_placental	dbNSFP_phyloP46way_placental_rankscore	dbNSFP_phyloP46way_primate	dbNSFP_phyloP46way_primate_rankscore	dbNSFP_refcodon	gencode_transcript_name	gencode_transcript_status	gencode_transcript_tags	gencode_transcript_type	gene_id	gene_type	havana_transcript	secondary_variant_classification	strand	transcript_id	variant_classification	variant_type	key	t_ref_count	t_alt_count
CYP4A11	1579	broad.mit.edu	37	1	47407091	47407091	+	Silent	SNP	C	C	G			TCGA-HZ-8638-01A-11D-2396-08	TCGA-HZ-8638-10A-01D-2396-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	08f8e370-782c-48de-989b-b861fafa9155	380736fb-bc7c-4d24-b8d8-66441c315ed4	g.chr1:47407091C>G	ENST00000310638.4	-	1	46	c.15G>C	c.(13-15)gtG>gtC	p.V5V	CYP4A11_ENST00000457840.2_5'UTR|CYP4A11_ENST00000371905.1_Silent_p.V5V|CYP4A11_ENST00000371904.4_Silent_p.V5V|CYP4A11_ENST00000462347.1_Silent_p.V5V	NM_000778.3	NP_000769.2	Q02928	CP4AB_HUMAN	cytochrome P450, family 4, subfamily A, polypeptide 11	5				V -> A (in Ref. 8; AA sequence).	long-chain fatty acid metabolic process|xenobiotic metabolic process	endoplasmic reticulum membrane|microsome	alkane 1-monooxygenase activity|electron carrier activity|heme binding|oxygen binding			endometrium(2)|kidney(5)|large_intestine(6)|lung(6)|ovary(5)|prostate(3)|skin(6)|soft_tissue(1)|upper_aerodigestive_tract(2)	36					NADH(DB00157)	TGGGGCTCAGCACAGAGACAC	0.587		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													83	83	83			NA	NA	1		NA											NA				47407091		2203	4300	6503	SO:0001819	synonymous_variant			L04751	CCDS543.1	1p33	2008-02-05	2003-01-14		ENSG00000187048	ENSG00000187048	1579	1579		Cytochrome P450s	2642	protein-coding gene	gene with protein product		601310	cytochrome P450, subfamily IVA, polypeptide 11	CYP4A2	NA	7679927	Standard	NM_000778	NM_000778	NA	Approved	CYP4AII	uc001cqp.4	Q02928	OTTHUMG00000008020	ENST00000310638.4:c.15G>C	1.37:g.47407091C>G		NA	Q06766|Q16865|Q16866|Q5VSP8|Q86SU6|Q8IWY5	37	CCDS543.1																																																																																			CYP4A11-001	KNOWN	basic|appris_candidate|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000022022.1		-	ENST00000310638.4	Silent	SNP	1 : 47407091 - 47407091 G PAAD-TCGA-HZ-8638-Tumor-SM-3MVD3	522	13
ERAP1	51752	broad.mit.edu	37	5	96122218	96122218	+	Missense_Mutation	SNP	C	C	T			TCGA-HZ-8638-01A-11D-2396-08	TCGA-HZ-8638-10A-01D-2396-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	08f8e370-782c-48de-989b-b861fafa9155	380736fb-bc7c-4d24-b8d8-66441c315ed4	g.chr5:96122218C>T	ENST00000296754.3	-	12	1972	c.1715G>A	c.(1714-1716)aGc>aAc	p.S572N	ERAP1_ENST00000514604.1_5'UTR|ERAP1_ENST00000443439.2_Missense_Mutation_p.S572N	NM_016442.3	NP_057526.3	Q9NZ08	ERAP1_HUMAN	endoplasmic reticulum aminopeptidase 1	572					angiogenesis|antigen processing and presentation of endogenous peptide antigen via MHC class I|fat cell differentiation|membrane protein ectodomain proteolysis|regulation of blood pressure|regulation of innate immune response|response to bacterium	cytosol|endoplasmic reticulum lumen|endoplasmic reticulum membrane|extracellular region|integral to membrane	aminopeptidase activity|interleukin-1, Type II receptor binding|interleukin-6 receptor binding|metalloexopeptidase activity|zinc ion binding			endometrium(7)|large_intestine(5)|lung(3)|ovary(1)|pancreas(1)|stomach(2)	19		all_cancers(142;1.75e-06)|all_epithelial(76;3.08e-09)|all_lung(232;0.000435)|Lung NSC(167;0.000601)|Ovarian(225;0.024)|Colorectal(57;0.0432)|Breast(839;0.244)		all cancers(79;7.26e-15)|COAD - Colon adenocarcinoma(37;0.071)		GTCGGATTTGCTGGTGATGAA	0.348		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													117	113	114			NA	NA	5		NA											NA				96122218		2203	4300	6503	SO:0001583	missense			AB011097	CCDS4085.1, CCDS47250.1	5q15	2014-04-07			ENSG00000164307	ENSG00000164307	51752	51752			18173	protein-coding gene	gene with protein product	aminopeptidase regulator of TNFR1 shedding, adipocyte-derived leucine aminopeptidase, puromycin-insensitive leucyl-specific aminopeptidase	606832			NA	10220586, 12189246, 16286653	Standard	NM_016442	NM_001198541	NA	Approved	ARTS-1, A-LAP, PILS-AP, KIAA0525, ERAAP1	uc003kml.3	Q9NZ08	OTTHUMG00000128721	ENST00000296754.3:c.1715G>A	5.37:g.96122218C>T	ENSP00000296754:p.Ser572Asn	NA	O60278|Q6UWY6|Q8NEL4|Q8TAD0|Q9UHF8|Q9UKY2	37	CCDS4085.1	.	.	.	.	.	.	.	.	.	.	C	14.70	2.612513	0.46631	.	.	ENSG00000164307	ENST00000296754;ENST00000443439;ENST00000414384	T;T	0.01369	4.97;4.97	5.33	5.33	0.75918	.	0.226724	0.51477	D	0.000090	T	0.03263	0.0095	L	0.58354	1.805	0.54753	D	0.999985	B;B;B	0.28400	0.013;0.028;0.21	B;B;B	0.33799	0.016;0.023;0.17	T	0.54262	-0.8320	10	0.40728	T	0.16	.	18.6209	0.91321	0.0:1.0:0.0:0.0	.	572;572;572	A8K6H1;Q9NZ08;Q9NZ08-2	.;ERAP1_HUMAN;.	N	572	ENSP00000296754:S572N;ENSP00000406304:S572N	ENSP00000296754:S572N	S	-	2	0	ERAP1	96147974	1.000000	0.71417	1.000000	0.80357	0.623000	0.37688	4.394000	0.59671	2.500000	0.84329	0.484000	0.47621	AGC	ERAP1-001	KNOWN	basic|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000250626.1		-	ENST00000296754.3	Missense_Mutation	SNP	5 : 96122218 - 96122218 T PAAD-TCGA-HZ-8638-Tumor-SM-3MVD3	190	7
KMT2C	58508	broad.mit.edu	37	7	151935851	151935851	+	Missense_Mutation	SNP	C	C	A			TCGA-HZ-8638-01A-11D-2396-08	TCGA-HZ-8638-10A-01D-2396-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	08f8e370-782c-48de-989b-b861fafa9155	380736fb-bc7c-4d24-b8d8-66441c315ed4	g.chr7:151935851C>A	ENST00000262189.6	-	15	2811	c.2593G>T	c.(2593-2595)Ggt>Tgt	p.G865C	KMT2C_ENST00000355193.2_Missense_Mutation_p.G865C	NM_170606.2	NP_733751.2			lysine (K)-specific methyltransferase 2C	NA											NA						ATTTCCCGACCTTCTGAAATG	0.423		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													49	52	51			NA	NA	7		NA											NA				151935851		2201	4300	6501	SO:0001583	missense			AF264750	CCDS5931.1	7q36	2013-05-09	2013-05-09	2013-05-09	ENSG00000055609	ENSG00000055609	58508	58508		Chromatin-modifying enzymes / K-methyltransferases, Zinc fingers, PHD-type	13726	protein-coding gene	gene with protein product		606833	myeloid/lymphoid or mixed-lineage leukemia 3	MLL3	NA	10819331	Standard		XM_005250026	NA	Approved	KIAA1506, HALR		Q8NEZ4	OTTHUMG00000150553	ENST00000262189.6:c.2593G>T	7.37:g.151935851C>A	ENSP00000262189:p.Gly865Cys	NA		37	CCDS5931.1	.	.	.	.	.	.	.	.	.	.	C	19.14	3.770503	0.69992	.	.	ENSG00000055609	ENST00000262189;ENST00000355193	D;D	0.86030	-2.06;-2.06	5.53	5.53	0.82687	.	0.000000	0.45126	D	0.000398	D	0.91395	0.7285	L	0.56769	1.78	0.80722	D	1	D	0.89917	1.0	D	0.76575	0.988	D	0.91517	0.5231	10	0.72032	D	0.01	.	19.8258	0.96617	0.0:1.0:0.0:0.0	.	865	Q8NEZ4	MLL3_HUMAN	C	865	ENSP00000262189:G865C;ENSP00000347325:G865C	ENSP00000262189:G865C	G	-	1	0	MLL3	151566784	1.000000	0.71417	1.000000	0.80357	0.999000	0.98932	7.442000	0.80503	2.749000	0.94314	0.650000	0.86243	GGT	KMT2C-001	KNOWN	basic|appris_candidate|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000318887.3		-	ENST00000262189.6	Missense_Mutation	SNP	7 : 151935851 - 151935851 A PAAD-TCGA-HZ-8638-Tumor-SM-3MVD3	594	15
LPIN2	9663	broad.mit.edu	37	18	2922157	2922157	+	Missense_Mutation	SNP	C	C	T			TCGA-HZ-8638-01A-11D-2396-08	TCGA-HZ-8638-10A-01D-2396-08	C	C	-	-	C	C	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	08f8e370-782c-48de-989b-b861fafa9155	380736fb-bc7c-4d24-b8d8-66441c315ed4	g.chr18:2922157C>T	ENST00000261596.4	-	17	2453	c.2215G>A	c.(2215-2217)Ggc>Agc	p.G739S		NM_014646.2	NP_055461.1	Q92539	LPIN2_HUMAN	lipin 2	739	C-LIP.				fatty acid metabolic process|positive regulation of transcription from RNA polymerase II promoter|transcription, DNA-dependent|triglyceride biosynthetic process	cytosol|endoplasmic reticulum membrane|nucleus	phosphatidate phosphatase activity|transcription coactivator activity			autonomic_ganglia(1)|breast(1)|endometrium(2)|large_intestine(4)|lung(16)|ovary(1)|pancreas(1)|prostate(2)|skin(1)	29				READ - Rectum adenocarcinoma(2;0.0419)|Colorectal(6;0.156)		TCGGCCATGCCGATGGCACGA	0.542		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													40	43	42			NA	NA	18		NA											NA				2922157		2203	4300	6503	SO:0001583	missense			D87436	CCDS11829.1	18p	2014-09-17			ENSG00000101577	ENSG00000101577	9663	9663			14450	protein-coding gene	gene with protein product		605519			NA	11138012, 9039502	Standard	NM_014646	NM_014646	NA	Approved	KIAA0249	uc002klo.3	Q92539	OTTHUMG00000131508	ENST00000261596.4:c.2215G>A	18.37:g.2922157C>T	ENSP00000261596:p.Gly739Ser	NA	A7MD25|D3DUH3	37	CCDS11829.1	.	.	.	.	.	.	.	.	.	.	C	36	5.852247	0.97023	.	.	ENSG00000101577	ENST00000261596	T	0.78126	-1.15	5.69	5.69	0.88448	HAD-like domain (2);LNS2, Lipin/Ned1/Smp2 (2);	0.000000	0.85682	D	0.000000	T	0.82038	0.4950	M	0.64080	1.96	0.80722	D	1	D	0.59767	0.986	P	0.50378	0.639	T	0.80618	-0.1302	10	0.36615	T	0.2	-24.9133	19.8167	0.96571	0.0:1.0:0.0:0.0	.	739	Q92539	LPIN2_HUMAN	S	739	ENSP00000261596:G739S	ENSP00000261596:G739S	G	-	1	0	LPIN2	2912157	1.000000	0.71417	0.993000	0.49108	0.961000	0.63080	7.398000	0.79919	2.679000	0.91253	0.563000	0.77884	GGC	LPIN2-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000254363.2		-	ENST00000261596.4	Missense_Mutation	SNP	18 : 2922157 - 2922157 T PAAD-TCGA-HZ-8638-Tumor-SM-3MVD3	232	6
OR2M5	127059	broad.mit.edu	37	1	248309032	248309032	+	Missense_Mutation	SNP	T	T	G			TCGA-HZ-8638-01A-11D-2396-08	TCGA-HZ-8638-10A-01D-2396-08	T	T	-	-	T	T	Unknown	Untested	Somatic	NA	WXS	none	NA	NA	Illumina HiSeq	08f8e370-782c-48de-989b-b861fafa9155	380736fb-bc7c-4d24-b8d8-66441c315ed4	g.chr1:248309032T>G	ENST00000366476.1	+	1	583	c.583T>G	c.(583-585)Ttt>Gtt	p.F195V		NM_001004690.1	NP_001004690.1	A3KFT3	OR2M5_HUMAN	olfactory receptor, family 2, subfamily M, member 5	195					sensory perception of smell	integral to membrane|plasma membrane	olfactory receptor activity			NS(1)|endometrium(5)|kidney(2)|large_intestine(7)|liver(1)|lung(25)|ovary(2)|pancreas(1)|prostate(1)|skin(2)|upper_aerodigestive_tract(2)	49	all_cancers(71;0.000149)|all_epithelial(71;1.27e-05)|Breast(184;0.00909)|Ovarian(71;0.0377)|all_lung(81;0.127)|Lung NSC(105;0.136)		OV - Ovarian serous cystadenocarcinoma(106;0.0388)			CACATCAATATTTGAAAAGGT	0.413		NA												NA	NA	NA	NA	NA	NA	NA			NA	NA	NA	NA	NA	NA	NA		NA	NA	NA									NA				0													265	260	262			NA	NA	1		NA											NA				248309032		2203	4300	6503	SO:0001583	missense				CCDS31105.1	1q44	2012-08-09		2004-03-10	ENSG00000162727	ENSG00000162727	127059	127059		GPCR / Class A : Olfactory receptors	19576	protein-coding gene	gene with protein product				OR2M5P	NA		Standard	NM_001004690	NM_001004690	NA	Approved		uc010pze.2	A3KFT3	OTTHUMG00000040447	ENST00000366476.1:c.583T>G	1.37:g.248309032T>G	ENSP00000355432:p.Phe195Val	NA		37	CCDS31105.1	.	.	.	.	.	.	.	.	.	.	t	17.11	3.306046	0.60305	.	.	ENSG00000162727	ENST00000366476	T	0.00058	8.79	3.52	-0.472	0.12115	GPCR, rhodopsin-like superfamily (1);	0.000000	0.32935	U	0.005464	T	0.00178	0.0005	L	0.27944	0.81	0.09310	N	1	P	0.50369	0.934	P	0.59643	0.861	T	0.51348	-0.8717	10	0.87932	D	0	.	3.1108	0.06357	0.3969:0.2566:0.0:0.3465	.	195	A3KFT3	OR2M5_HUMAN	V	195	ENSP00000355432:F195V	ENSP00000355432:F195V	F	+	1	0	OR2M5	246375655	0.173000	0.23056	0.041000	0.18516	0.397000	0.30659	0.092000	0.15066	0.359000	0.24239	0.403000	0.27427	TTT	OR2M5-001	KNOWN	basic|appris_principal|CCDS	protein_coding	NA	protein_coding	OTTHUMT00000097343.1		+	ENST00000366476.1	Missense_Mutation	SNP	1 : 248309032 - 248309032 G PAAD-TCGA-HZ-8638-Tumor-SM-3MVD3	1667	26
