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 PABPC4 8761 broad.mit.edu 37 1 40027846 40027846 + Missense_Mutation SNP T T C rs141368472 TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:40027846T>C ENST00000372857.3 - 14 2536 c.1744A>G c.(1744-1746)Atg>Gtg p.M582V PABPC4_ENST00000372862.3_Missense_Mutation_p.M553V|PABPC4_ENST00000372856.3_Missense_Mutation_p.M569V|PABPC4_ENST00000372858.3_Missense_Mutation_p.M598V NM_003819.3 NP_003810.1 Q13310 PABP4_HUMAN poly(A) binding protein, cytoplasmic 4 (inducible form) 582 PABC. blood coagulation|RNA catabolic process|RNA processing|translation cytoplasm|ribonucleoprotein complex nucleotide binding|poly(A) RNA binding|poly(U) RNA binding|protein binding p.M582V(1) NS(1)|breast(1)|central_nervous_system(1)|endometrium(1)|kidney(1)|large_intestine(5)|liver(1)|lung(6)|prostate(1)|skin(3) 21 Lung NSC(20;1.55e-06)|Ovarian(52;0.00769)|all_hematologic(146;0.0501)|Acute lymphoblastic leukemia(166;0.074) Myeloproliferative disorder(586;0.0255) OV - Ovarian serous cystadenocarcinoma(33;2.89e-18)|Epithelial(16;6.17e-17)|all cancers(16;1.18e-15)|LUSC - Lung squamous cell carcinoma(16;0.000261)|Lung(16;0.000457) TTTGAATGCATTGTTTGGATG 0.473 5 141 --- --- --- --- SZT2 23334 broad.mit.edu 37 1 43897409 43897409 + Missense_Mutation SNP A A G TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:43897409A>G ENST00000562955.1 + 35 4940 c.4940A>G c.(4939-4941)gAg>gGg p.E1647G SZT2_ENST00000372442.1_Missense_Mutation_p.E805G NM_015284.3 NP_056099.3 Q5T011 SZT2_HUMAN seizure threshold 2 homolog (mouse) 1704 peroxisome p.E805G(2) NS(2)|breast(9)|central_nervous_system(1)|endometrium(17)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(19)|lung(39)|ovary(4)|pancreas(3)|prostate(4)|skin(2)|stomach(1)|upper_aerodigestive_tract(4)|urinary_tract(3) 113 TTGGAAGATGAGATGGTGGGG 0.567 3 162 --- --- --- --- RSBN1 54665 broad.mit.edu 37 1 114319949 114319949 + Missense_Mutation SNP G G C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:114319949G>C ENST00000261441.5 - 4 1604 c.1541C>G c.(1540-1542)tCt>tGt p.S514C NM_018364.3 NP_060834.2 Q5VWQ0 RSBN1_HUMAN round spermatid basic protein 1 514 nucleus p.S514C(1) breast(1)|endometrium(2)|large_intestine(4)|lung(16)|ovary(1)|prostate(3)|urinary_tract(2) 29 Lung SC(450;0.184) all_cancers(81;3.78e-08)|all_epithelial(167;5.56e-08)|all_lung(203;6.97e-06)|Lung NSC(69;1.18e-05) Lung(183;0.0234)|Colorectal(144;0.0686)|all cancers(265;0.0792)|Epithelial(280;0.0866)|COAD - Colon adenocarcinoma(174;0.111)|LUSC - Lung squamous cell carcinoma(189;0.133) TCGGAGGCTAGAAAGTGTACC 0.428 40 188 --- --- --- --- CFH 3075 broad.mit.edu 37 1 196695918 196695918 + Missense_Mutation SNP C C A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:196695918C>A ENST00000367429.4 + 14 2324 c.2084C>A c.(2083-2085)cCt>cAt p.P695H NM_000186.3 NP_000177.2 P08603 CFAH_HUMAN complement factor H 695 Sushi 12. complement activation, alternative pathway extracellular space p.P695H(1) NS(3)|breast(4)|endometrium(6)|haematopoietic_and_lymphoid_tissue(2)|kidney(8)|large_intestine(24)|lung(33)|ovary(1)|prostate(5)|skin(9)|stomach(3)|upper_aerodigestive_tract(1)|urinary_tract(2) 101 GGAGATATACCTGAACTTGAA 0.353 29 169 --- --- --- --- ASPM 259266 broad.mit.edu 37 1 197104365 197104365 + Silent SNP G G C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:197104365G>C ENST00000367409.4 - 5 2290 c.2034C>G c.(2032-2034)ccC>ccG p.P678P ASPM_ENST00000294732.7_Silent_p.P678P NM_018136.4 NP_060606.3 Q8IZT6 ASPM_HUMAN asp (abnormal spindle) homolog, microcephaly associated (Drosophila) 678 mitosis cytoplasm|nucleus calmodulin binding p.P678P(1) breast(6)|central_nervous_system(2)|cervix(2)|endometrium(10)|kidney(9)|large_intestine(28)|liver(1)|lung(87)|ovary(5)|pancreas(2)|prostate(6)|skin(4)|urinary_tract(3) 165 TCGGGTGTCTGGGAATATCTA 0.333 12 100 --- --- --- --- OBSCN 84033 broad.mit.edu 37 1 228462137 228462137 + Missense_Mutation SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:228462137C>T ENST00000570156.2 + 23 6874 c.6800C>T c.(6799-6801)aCc>aTc p.T2267I OBSCN_ENST00000422127.1_Missense_Mutation_p.T1892I|OBSCN_ENST00000366709.4_5'UTR|OBSCN_ENST00000359599.6_Missense_Mutation_p.T739I|OBSCN_ENST00000366707.4_5'UTR|OBSCN_ENST00000284548.11_Missense_Mutation_p.T1892I NM_001271223.2 NP_001258152.2 Q5VST9 OBSCN_HUMAN obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF 1250 apoptosis|cell differentiation|induction of apoptosis by extracellular signals|multicellular organismal development|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction cytosol|M band|Z disc ATP binding|metal ion binding|protein binding|protein serine/threonine kinase activity|protein tyrosine kinase activity|Rho guanyl-nucleotide exchange factor activity|structural constituent of muscle|titin binding p.T2175I(1)|p.T1892I(1) NS(2)|breast(7)|central_nervous_system(5)|cervix(2)|endometrium(30)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(37)|lung(89)|ovary(8)|pancreas(3)|prostate(13)|skin(6)|stomach(11)|upper_aerodigestive_tract(2)|urinary_tract(3) 223 Prostate(94;0.0405) GCGCAGCTCACCGTCAGTGGT 0.642 6 32 --- --- --- --- GNPAT 8443 broad.mit.edu 37 1 231377146 231377146 + Missense_Mutation SNP A A G TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr1:231377146A>G ENST00000366647.4 + 1 191 c.22A>G c.(22-24)Aac>Gac p.N8D GNPAT_ENST00000366646.3_Missense_Mutation_p.N8D NM_014236.3 NP_055051.1 O15228 GNPAT_HUMAN glyceronephosphate O-acyltransferase 8 Poly-Ser. ether lipid biosynthetic process|fatty acid metabolic process|organ morphogenesis peroxisomal matrix|peroxisomal membrane glycerone-phosphate O-acyltransferase activity p.N8D(1) breast(2)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(2)|lung(9)|ovary(3)|prostate(1)|skin(1) 23 Breast(184;0.0871) all_cancers(173;0.2)|Prostate(94;0.183) CAGTTCATCTAACTCTTATTT 0.617 26 162 --- --- --- --- USP34 9736 broad.mit.edu 37 2 61415488 61415488 + Nonsense_Mutation SNP C C A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr2:61415488C>A ENST00000398571.2 - 80 10466 c.10390G>T c.(10390-10392)Gaa>Taa p.E3464* AHSA2_ENST00000394457.3_3'UTR NM_014709.3 NP_055524.3 Q70CQ2 UBP34_HUMAN ubiquitin specific peptidase 34 3464 positive regulation of canonical Wnt receptor signaling pathway|protein K48-linked deubiquitination|ubiquitin-dependent protein catabolic process|Wnt receptor signaling pathway cysteine-type endopeptidase activity|protein binding|ubiquitin thiolesterase activity|ubiquitin-specific protease activity p.E3464*(1) autonomic_ganglia(1)|breast(14)|cervix(1)|endometrium(9)|haematopoietic_and_lymphoid_tissue(1)|kidney(10)|large_intestine(24)|lung(52)|ovary(8)|prostate(10)|skin(6)|urinary_tract(2) 138 Epithelial(17;0.229) TCAGATTCTTCCTCAGCTAGG 0.463 4 157 --- --- --- --- KYNU 8942 broad.mit.edu 37 2 143790837 143790837 + Nonsense_Mutation SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr2:143790837C>T ENST00000264170.4 + 12 1246 c.988C>T c.(988-990)Cga>Tga p.R330* KYNU_ENST00000409512.1_Nonsense_Mutation_p.R330* NM_003937.2 NP_003928.1 Q16719 KYNU_HUMAN kynureninase 330 anthranilate metabolic process|NAD biosynthetic process|quinolinate biosynthetic process|response to interferon-gamma|response to vitamin B6 cytosol|mitochondrion|soluble fraction kynureninase activity|protein homodimerization activity p.R330*(1) large_intestine(10)|liver(1)|lung(18)|prostate(3)|skin(4) 36 BRCA - Breast invasive adenocarcinoma(221;0.072) L-Alanine(DB00160)|Pyridoxal Phosphate(DB00114) CTGTGGATTCCGAATTTCAAA 0.373 63 486 --- --- --- --- SP140L 93349 broad.mit.edu 37 2 231222557 231222557 + Missense_Mutation SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr2:231222557G>T ENST00000243810.6 + 3 145 c.145G>T c.(145-147)Gtc>Ttc p.V49F SP140L_ENST00000396563.4_Missense_Mutation_p.V49F|SP140_ENST00000486687.2_3'UTR|SP140L_ENST00000444636.1_Missense_Mutation_p.V49F|SP140L_ENST00000415673.2_Missense_Mutation_p.V49F|SP140L_ENST00000458341.1_5'UTR Q9H930 LY10L_HUMAN SP140 nuclear body protein-like 49 HSR. nucleus DNA binding|metal ion binding p.V49F(1) central_nervous_system(1)|endometrium(1)|kidney(4)|large_intestine(5)|lung(7)|prostate(1)|skin(1) 20 TGAGGGACTTGTCTATGACAC 0.423 14 454 --- --- --- --- SETD2 29072 broad.mit.edu 37 3 47163433 47163433 + Missense_Mutation SNP A A C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr3:47163433A>C ENST00000409792.3 - 3 2735 c.2693T>G c.(2692-2694)tTg>tGg p.L898W NM_014159.6 NP_054878.5 Q9BYW2 SETD2_HUMAN SET domain containing 2 898 regulation of transcription, DNA-dependent|transcription, DNA-dependent chromosome|nucleus DNA binding|histone-lysine N-methyltransferase activity|oxidoreductase activity|transition metal ion binding p.L395W(1)|p.L898W(1) breast(6)|central_nervous_system(5)|endometrium(4)|kidney(63)|large_intestine(18)|lung(26)|ovary(6)|prostate(2)|skin(3)|soft_tissue(1)|stomach(2)|urinary_tract(5) 141 Acute lymphoblastic leukemia(5;0.0169) BRCA - Breast invasive adenocarcinoma(193;0.000302)|KIRC - Kidney renal clear cell carcinoma(197;0.00732)|Kidney(197;0.00844) TCCGCATTTCAAGAGAGTTAG 0.378 """N, F, S, Mis""" clear cell renal carcinoma 8 273 --- --- --- --- MYH15 22989 broad.mit.edu 37 3 108112995 108112995 + Silent SNP G G A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr3:108112995G>A ENST00000273353.3 - 37 5258 c.5202C>T c.(5200-5202)agC>agT p.S1734S NM_014981.1 NP_055796.1 Q9Y2K3 MYH15_HUMAN myosin, heavy chain 15 1734 myofibril|myosin filament actin binding|ATP binding|calmodulin binding|motor activity p.S1734S(1) NS(1)|breast(3)|central_nervous_system(2)|cervix(4)|endometrium(10)|kidney(4)|large_intestine(14)|lung(47)|ovary(5)|pancreas(2)|prostate(6)|skin(2)|stomach(1)|upper_aerodigestive_tract(2)|urinary_tract(2) 105 GGCTGAGGAGGCTTGTGTTCT 0.478 30 150 --- --- --- --- FAM134B 54463 broad.mit.edu 37 5 16475005 16475005 + Missense_Mutation SNP T T C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr5:16475005T>C ENST00000306320.9 - 9 1425 c.1339A>G c.(1339-1341)Aca>Gca p.T447A FAM134B_ENST00000399793.2_Missense_Mutation_p.T306A NM_001034850.2 NP_001030022.1 Q9H6L5 F134B_HUMAN family with sequence similarity 134, member B 447 sensory perception of pain cis-Golgi network|endoplasmic reticulum|integral to membrane p.T447A(1) breast(1)|kidney(1)|large_intestine(4)|lung(5)|ovary(2)|prostate(2)|skin(1) 16 TCAGTGTCTGTGTCCTCTTCT 0.493 21 133 --- --- --- --- LOC101929006 101929006 broad.mit.edu 37 6 29230640 29230640 + RNA SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr6:29230640G>T ENST00000441381.1 + 0 79 p.A240E(1) GGTCCCAAATGCTTTTTGTCT 0.418 21 134 --- --- --- --- VARS2 57176 broad.mit.edu 37 6 30884893 30884893 + Silent SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr6:30884893G>T ENST00000321897.5 + 8 1397 c.765G>T c.(763-765)gtG>gtT p.V255V VARS2_ENST00000416670.2_Silent_p.V255V|VARS2_ENST00000542001.1_Silent_p.V115V|VARS2_ENST00000541562.1_Silent_p.V285V Q5ST30 SYVM_HUMAN valyl-tRNA synthetase 2, mitochondrial 255 valyl-tRNA aminoacylation mitochondrion ATP binding|valine-tRNA ligase activity p.V255V(1) central_nervous_system(2)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(2)|kidney(5)|large_intestine(9)|lung(15)|ovary(3)|prostate(3)|skin(4)|urinary_tract(1) 46 GCTCCTCAGTGGCTGTGACTG 0.567 4 159 --- --- --- --- EHMT2 10919 broad.mit.edu 37 6 31850727 31850727 + Missense_Mutation SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr6:31850727G>T ENST00000395728.3 - 23 3224 c.3225C>A c.(3223-3225)aaC>aaA p.N1075K EHMT2_ENST00000480912.1_5'UTR|EHMT2_ENST00000375537.4_Missense_Mutation_p.N1018K|EHMT2_ENST00000375530.4_Missense_Mutation_p.N984K|EHMT2_ENST00000375528.4_Missense_Mutation_p.N1041K Q96KQ7 EHMT2_HUMAN euchromatic histone-lysine N-methyltransferase 2 1018 Interaction with histone H3 (By similarity).|SET. DNA methylation|peptidyl-lysine dimethylation chromosome|nucleus histone methyltransferase activity (H3-K27 specific)|histone methyltransferase activity (H3-K9 specific)|p53 binding|zinc ion binding p.N1018K(1) central_nervous_system(1)|cervix(2)|kidney(2)|large_intestine(3)|lung(6)|ovary(2)|prostate(4)|upper_aerodigestive_tract(1) 21 AGCACGCCTGGTTACACTCGA 0.572 4 76 --- --- --- --- GLTSCR1L 23506 broad.mit.edu 37 6 42824964 42824964 + Missense_Mutation SNP C C A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr6:42824964C>A ENST00000314073.5 + 10 2420 c.2244C>A c.(2242-2244)gaC>gaA p.D748E GLTSCR1L_ENST00000394168.1_Missense_Mutation_p.D748E GLTSCR1-like p.D748E(1) CTGAAGAAGACTTGAGAAAAG 0.542 20 131 --- --- --- --- PKHD1 5314 broad.mit.edu 37 6 51889566 51889566 + Missense_Mutation SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr6:51889566G>T ENST00000371117.3 - 32 5317 c.5042C>A c.(5041-5043)gCa>gAa p.A1681E PKHD1_ENST00000340994.4_Missense_Mutation_p.A1681E NM_138694.3 NP_619639.3 P08F94 PKHD1_HUMAN polycystic kidney and hepatic disease 1 (autosomal recessive) 1681 IPT/TIG 12; atypical. 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 p.A1681E(1) 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) GTCAATGTTTGCAGCTCCTGA 0.493 4 177 --- --- --- --- DPY19L2P1 554236 broad.mit.edu 37 7 35142675 35142675 + RNA SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr7:35142675C>T ENST00000436258.1 - 0 1811 ATTATCAAAACGAACTCTGCG 0.338 3 73 --- --- --- --- PON1 5444 broad.mit.edu 37 7 94940824 94940824 + Missense_Mutation SNP A A C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr7:94940824A>C ENST00000222381.3 - 5 667 c.436T>G c.(436-438)Ttt>Gtt p.F146V PON1_ENST00000542556.1_Missense_Mutation_p.F146V NM_000446.5 NP_000437.3 P27169 PON1_HUMAN paraoxonase 1 146 aromatic compound catabolic process|carboxylic acid catabolic process|organophosphate catabolic process|phosphatidylcholine metabolic process|positive regulation of binding|positive regulation of cholesterol efflux|positive regulation of transporter activity|response to external stimulus spherical high-density lipoprotein particle aryldialkylphosphatase activity|arylesterase activity|calcium ion binding|phospholipid binding|protein homodimerization activity p.F146V(1) autonomic_ganglia(1)|endometrium(2)|large_intestine(6)|lung(11)|pancreas(3)|prostate(1)|stomach(1)|upper_aerodigestive_tract(2) 27 all_cancers(62;1.04e-10)|all_epithelial(64;3.67e-09)|Lung NSC(181;0.239) STAD - Stomach adenocarcinoma(171;0.0031) Atorvastatin(DB01076)|Cefazolin(DB01327) TCTTCTTGAAATTTAAACAAC 0.353 34 177 --- --- --- --- PIK3CG 5294 broad.mit.edu 37 7 106524649 106524649 + Missense_Mutation SNP T T C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr7:106524649T>C ENST00000359195.3 + 9 3120 c.2810T>C c.(2809-2811)gTg>gCg p.V937A PIK3CG_ENST00000440650.2_Missense_Mutation_p.V937A|PIK3CG_ENST00000496166.1_Missense_Mutation_p.V937A NM_001282427.1|NM_002649.2 NP_001269356.1|NP_002640.2 P48736 PK3CG_HUMAN phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma 937 PI3K/PI4K. G-protein coupled receptor protein signaling pathway|phosphatidylinositol-mediated signaling|platelet activation phosphatidylinositol 3-kinase complex 1-phosphatidylinositol-3-kinase activity|ATP binding|phosphatidylinositol-4,5-bisphosphate 3-kinase activity|protein binding p.V937A(2) breast(7)|central_nervous_system(9)|cervix(1)|endometrium(6)|kidney(4)|large_intestine(16)|liver(4)|lung(59)|ovary(4)|pancreas(4)|prostate(3)|skin(6)|stomach(3)|upper_aerodigestive_tract(5)|urinary_tract(1) 132 GGCTACTGTGTGGCAACCTTT 0.368 48 267 --- --- --- --- RP1 6101 broad.mit.edu 37 8 55537506 55537506 + Missense_Mutation SNP A A T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr8:55537506A>T ENST00000220676.1 + 4 1212 c.1064A>T c.(1063-1065)aAa>aTa p.K355I NM_006269.1 NP_006260.1 P56715 RP1_HUMAN retinitis pigmentosa 1 (autosomal dominant) 355 axoneme assembly|intracellular signal transduction|photoreceptor cell maintenance|photoreceptor cell outer segment organization|phototransduction, visible light|retinal cone cell development|retinal rod cell development cilium axoneme|cytoplasm|microtubule|microtubule associated complex|photoreceptor connecting cilium|photoreceptor inner segment|photoreceptor outer segment microtubule binding p.K355I(1) NS(4)|breast(6)|central_nervous_system(2)|cervix(1)|endometrium(9)|haematopoietic_and_lymphoid_tissue(4)|kidney(7)|large_intestine(29)|lung(69)|ovary(6)|pancreas(1)|prostate(9)|skin(17)|upper_aerodigestive_tract(3)|urinary_tract(2) 169 all_lung(136;0.0831)|Lung NSC(129;0.109)|all_epithelial(80;0.123) OV - Ovarian serous cystadenocarcinoma(7;4.4e-07)|Epithelial(17;3.37e-05)|all cancers(17;0.000285) ACTGTCAGTAAAACTGGTCCT 0.353 10 60 --- --- --- --- LCN12 286256 broad.mit.edu 37 9 139847394 139847394 + Silent SNP G G A rs62580418 TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr9:139847394G>A ENST00000371633.3 + 2 165 c.165G>A c.(163-165)ccG>ccA p.P55P NM_178536.3 NP_848631.2 Q6JVE5 LCN12_HUMAN lipocalin 12 55 lipid metabolic process extracellular region binding|transporter activity p.P55P(1) endometrium(1)|kidney(1)|lung(1)|prostate(2) 5 all_cancers(76;0.11) Myeloproliferative disorder(178;0.0511) STAD - Stomach adenocarcinoma(284;0.19) OV - Ovarian serous cystadenocarcinoma(145;7.8e-06)|Epithelial(140;0.000106) GCTTCAGGCCGGAGCACAGGG 0.637 39 233 --- --- --- --- LRIT2 340745 broad.mit.edu 37 10 85981795 85981795 + Missense_Mutation SNP C C A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr10:85981795C>A ENST00000372113.4 - 3 1539 c.1534G>T c.(1534-1536)Gca>Tca p.A512S LRIT2_ENST00000538192.1_Missense_Mutation_p.A522S NM_001017924.2 NP_001017924.1 A6NDA9 LRIT2_HUMAN leucine-rich repeat, immunoglobulin-like and transmembrane domains 2 512 integral to membrane p.A512S(1) central_nervous_system(1)|cervix(1)|endometrium(2)|kidney(1)|large_intestine(4)|lung(13)|ovary(3)|prostate(6)|urinary_tract(1) 32 TGCGGGGCTGCAGGGGTGCAG 0.627 4 157 --- --- --- --- CAPZA3 93661 broad.mit.edu 37 12 18891209 18891209 + Missense_Mutation SNP C C G TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr12:18891209C>G ENST00000317658.3 + 1 165 c.7C>G c.(7-9)Ctt>Gtt p.L3V NM_033328.2 NP_201585.1 Q96KX2 CAZA3_HUMAN capping protein (actin filament) muscle Z-line, alpha 3 3 actin cytoskeleton organization|actin filament capping F-actin capping protein complex actin binding p.L3V(1) breast(1)|central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(5)|liver(1)|lung(6)|ovary(1)|prostate(1) 19 Acute lymphoblastic leukemia(4;0.000455)|all_hematologic(4;0.0241) Hepatocellular(102;0.194) AAACATGACACTTAGCGTGCT 0.438 4 201 --- --- --- --- OR6C76 390326 broad.mit.edu 37 12 55820712 55820712 + Silent SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr12:55820712C>T ENST00000328314.3 + 1 675 c.675C>T c.(673-675)atC>atT p.I225I NM_001005183.1 NP_001005183.1 A6NM76 O6C76_HUMAN olfactory receptor, family 6, subfamily C, member 76 225 sensory perception of smell integral to membrane|plasma membrane olfactory receptor activity p.I225I(1) NS(1)|central_nervous_system(1)|large_intestine(3)|lung(4)|prostate(1)|skin(1)|soft_tissue(1)|upper_aerodigestive_tract(1)|urinary_tract(1) 14 TTCTGAGAATCCCCTCAGCAC 0.363 18 108 --- --- --- --- C12orf55 144535 broad.mit.edu 37 12 97085090 97085090 + Splice_Site SNP T T A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr12:97085090T>A ENST00000524981.4 + 44 6287 c.e44+2 chromosome 12 open reading frame 55 AACCTAATAGTAAGTAATTTG 0.318 4 95 --- --- --- --- CLTC 1213 broad.mit.edu 37 17 57737855 57737855 + Missense_Mutation SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr17:57737855C>T ENST00000269122.3 + 7 1347 c.1073C>T c.(1072-1074)gCc>gTc p.A358V CLTC_ENST00000579456.1_Intron|CLTC_ENST00000393043.1_Missense_Mutation_p.A358V NM_004859.3 NP_004850.1 Q00610 CLH1_HUMAN clathrin, heavy chain (Hc) 358 Globular terminal domain. axon guidance|epidermal growth factor receptor signaling pathway|intracellular protein transport|mitosis|negative regulation of epidermal growth factor receptor signaling pathway|nerve growth factor receptor signaling pathway|post-Golgi vesicle-mediated transport|receptor internalization|transferrin transport clathrin coat of coated pit|clathrin coat of trans-Golgi network vesicle|cytosol|melanosome|spindle protein binding|structural molecule activity p.A358V(1) CLTC/ALK(44)|CLTC/TFE3(2) breast(2)|large_intestine(6)|ovary(1) 9 all_neural(34;0.0878)|Medulloblastoma(34;0.0922) AATAACTTAGCCGGTGCTGAA 0.433 T """ALK, TFE3""" """ALCL, renal """ 6 443 --- --- --- --- SERPINB5 5268 broad.mit.edu 37 18 61170910 61170910 + Missense_Mutation SNP C C A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr18:61170910C>A ENST00000382771.4 + 7 1375 c.1083C>A c.(1081-1083)aaC>aaA p.N361K NM_002639.4 NP_002630.2 P36952 SPB5_HUMAN serpin peptidase inhibitor, clade B (ovalbumin), member 5 361 cellular component movement|regulation of proteolysis cytoplasm|extracellular space protein binding|serine-type endopeptidase inhibitor activity kidney(3)|large_intestine(2)|lung(5)|ovary(1)|prostate(1) 12 TCAGGCACAACAAAACTCGAA 0.443 14 395 --- --- --- --- TSPAN16 26526 broad.mit.edu 37 19 11417404 11417404 + Missense_Mutation SNP A A G TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr19:11417404A>G ENST00000316737.1 + 5 725 c.575A>G c.(574-576)gAt>gGt p.D192G TSPAN16_ENST00000592955.1_Missense_Mutation_p.D167G|TSPAN16_ENST00000590327.1_Missense_Mutation_p.D192G|CTC-510F12.4_ENST00000586356.1_RNA NM_012466.2 NP_036598.1 Q9UKR8 TSN16_HUMAN tetraspanin 16 192 integral to membrane p.D192G(1) breast(1)|endometrium(3)|large_intestine(1)|lung(2)|ovary(1)|prostate(1)|skin(2)|stomach(1) 12 GACGGACGCGATGTGTCTCCA 0.473 5 78 --- --- --- --- CYP2A13 1553 broad.mit.edu 37 19 41596036 41596036 + Missense_Mutation SNP G G A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr19:41596036G>A ENST00000330436.3 + 3 428 c.428G>A c.(427-429)cGc>cAc p.R143H NM_000766.4 NP_000757.2 Q16696 CP2AD_HUMAN cytochrome P450, family 2, subfamily A, polypeptide 13 143 xenobiotic metabolic process endoplasmic reticulum membrane|microsome aromatase activity|coumarin 7-hydroxylase activity|electron carrier activity|heme binding p.R143H(1) breast(3)|endometrium(6)|kidney(4)|large_intestine(8)|lung(13)|ovary(3)|prostate(3)|skin(2) 42 Clomipramine(DB01242)|Nicotine(DB00184) GTGGGCAAGCGCGGCATCGAG 0.697 10 50 --- --- --- --- MYBPC2 4606 broad.mit.edu 37 19 50939044 50939044 + Missense_Mutation SNP G G A TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr19:50939044G>A ENST00000357701.5 + 3 172 c.121G>A c.(121-123)Gag>Aag p.E41K NM_004533.3 NP_004524.3 Q14324 MYPC2_HUMAN myosin binding protein C, fast type 41 cell adhesion|muscle filament sliding cytosol|myosin filament actin binding|structural constituent of muscle p.E41K(1) breast(1) 1 all_neural(266;0.057) OV - Ovarian serous cystadenocarcinoma(262;0.0079)|GBM - Glioblastoma multiforme(134;0.0144) AGCCCCACCCGAGGACCAGTC 0.627 8 20 --- --- --- --- ZNF579 163033 broad.mit.edu 37 19 56090151 56090151 + Silent SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr19:56090151C>T ENST00000325421.4 - 2 883 c.855G>A c.(853-855)ctG>ctA p.L285L NM_152600.2 NP_689813.2 Q8NAF0 ZN579_HUMAN zinc finger protein 579 285 regulation of transcription, DNA-dependent|transcription, DNA-dependent nucleus DNA binding|zinc ion binding p.L285L(1) endometrium(1)|lung(5)|prostate(1)|skin(1)|upper_aerodigestive_tract(1) 9 BRCA - Breast invasive adenocarcinoma(297;0.18) GBM - Glioblastoma multiforme(193;0.106) GGTGGCGCGACAGGGACCAGG 0.731 4 38 --- --- --- --- PEG3 5178 broad.mit.edu 37 19 57329201 57329201 + Missense_Mutation SNP G G T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr19:57329201G>T ENST00000326441.9 - 9 1138 c.775C>A c.(775-777)Cag>Aag p.Q259K PEG3_ENST00000598410.1_Missense_Mutation_p.Q135K|ZIM2_ENST00000391708.3_Intron|ZIM2_ENST00000221722.5_Intron|PEG3_ENST00000593695.1_Missense_Mutation_p.Q133K|ZIM2_ENST00000601070.1_Intron|ZIM2_ENST00000593711.1_Intron|ZIM2_ENST00000599935.1_Intron|PEG3_ENST00000423103.2_Missense_Mutation_p.Q259K NM_006210.2 NP_006201.1 Q9GZU2 PEG3_HUMAN paternally expressed 3 259 apoptosis|viral reproduction cytoplasm|nucleus nucleic acid binding|sequence-specific DNA binding transcription factor activity|zinc ion binding p.Q259K(2) 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) TCAGCAAGCTGCACTCCTGGT 0.488 5 41 --- --- --- --- RBL1 5933 broad.mit.edu 37 20 35668590 35668590 + Silent SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr20:35668590C>T ENST00000373664.3 - 14 1935 c.1869G>A c.(1867-1869)aaG>aaA p.K623K RBL1_ENST00000344359.3_Silent_p.K623K NM_002895.2 NP_002886.2 P28749 RBL1_HUMAN retinoblastoma-like 1 (p107) 623 Pocket; binds T and E1A.|Spacer. cell cycle|chromatin modification|interspecies interaction between organisms|regulation of cell cycle|regulation of lipid kinase activity|transcription, DNA-dependent transcription factor binding p.K623K(1) NS(1)|breast(1)|endometrium(7)|large_intestine(6)|lung(16)|ovary(2)|pancreas(1)|prostate(1)|skin(6)|upper_aerodigestive_tract(1) 42 Myeloproliferative disorder(115;0.00878) TTCGAACTTCCTTGACTCTTG 0.418 22 222 --- --- --- --- DSCAM 1826 broad.mit.edu 37 21 41684282 41684282 + Silent SNP C C T TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr21:41684282C>T ENST00000400454.1 - 9 2265 c.1788G>A c.(1786-1788)ccG>ccA p.P596P NM_001271534.1|NM_001389.3 NP_001258463.1|NP_001380.2 O60469 DSCAM_HUMAN Down syndrome cell adhesion molecule 596 Ig-like C2-type 7. cell adhesion|dendrite self-avoidance|negative regulation of cell adhesion|positive regulation of axon extension involved in axon guidance|positive regulation of phosphorylation axon|extracellular region|growth cone|integral to plasma membrane|membrane fraction protein binding p.P596P(2) NS(2)|breast(1)|central_nervous_system(1)|cervix(1)|endometrium(22)|haematopoietic_and_lymphoid_tissue(4)|kidney(6)|large_intestine(22)|lung(47)|ovary(7)|pancreas(2)|prostate(3)|skin(14)|upper_aerodigestive_tract(6)|urinary_tract(4) 142 all_cancers(19;0.186)|Prostate(19;1.15e-05)|all_epithelial(19;0.0103) GTATGAAAGGCGGAACTGCAA 0.448 5 26 --- --- --- --- ARHGAP6 395 broad.mit.edu 37 X 11204545 11204545 + Missense_Mutation SNP T T C TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chrX:11204545T>C ENST00000337414.4 - 5 1956 c.1084A>G c.(1084-1086)Atg>Gtg p.M362V ARHGAP6_ENST00000303025.6_Missense_Mutation_p.M159V|ARHGAP6_ENST00000380736.1_Missense_Mutation_p.M159V|ARHGAP6_ENST00000380718.1_Missense_Mutation_p.M362V|ARHGAP6_ENST00000534860.1_Missense_Mutation_p.M187V|ARHGAP6_ENST00000380732.3_Missense_Mutation_p.M394V|ARHGAP6_ENST00000413512.3_Missense_Mutation_p.M171V NM_013427.2 NP_038286.2 O43182 RHG06_HUMAN Rho GTPase activating protein 6 362 actin filament polymerization|activation of phospholipase C activity|negative regulation of focal adhesion assembly|negative regulation of stress fiber assembly|Rho protein signal transduction actin filament|cytosol phospholipase activator activity|phospholipase binding|Rho GTPase activator activity|SH3 domain binding|SH3/SH2 adaptor activity p.M362V(2) cervix(1)|endometrium(5)|kidney(1)|large_intestine(5)|lung(19)|ovary(1)|prostate(2)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(2) 38 TCCACTGACATGGCACCCTGC 0.443 58 123 --- --- --- --- AMZ2P1 201283 broad.mit.edu 37 17 62968909 62968909 + RNA DEL T T - TCGA-EJ-5498-01A-01D-1576-08 TCGA-EJ-5498-10A-01D-1577-08 Untested Somatic Phase_I WXS none Illumina GAIIx 3b4e02da-87be-46e2-b4bd-555ca1440808 b8daddf3-4dbc-47b1-b5bf-777c46131bb8 g.chr17:62968909delT ENST00000430983.1 - 0 1426 NR_026903.1 TCTCATTGACTCTAAAGGAAC 0.358 11 56 --- --- --- ---