Hugo_Symbol Entrez_Gene_Id Center NCBI_Build Chromosome Start_position End_position Strand Variant_Classification Variant_Type Reference_Allele Tumor_Seq_Allele1 Tumor_Seq_Allele2 dbSNP_RS dbSNP_Val_Status Tumor_Sample_Barcode Matched_Norm_Sample_Barcode Match_Norm_Seq_Allele1 Match_Norm_Seq_Allele2 Tumor_Validation_Allele1 Tumor_Validation_Allele2 Match_Norm_Validation_Allele1 Match_Norm_Validation_Allele2 Verification_Status Validation_Status Mutation_Status Sequencing_Phase Sequence_Source Validation_Method Score BAM_file Sequencer Tumor_Sample_UUID Matched_Norm_Sample_UUID Genome_Change Annotation_Transcript Transcript_Strand Transcript_Exon Transcript_Position cDNA_Change Codon_Change Protein_Change Other_Transcripts Refseq_mRNA_Id Refseq_prot_Id SwissProt_acc_Id SwissProt_entry_Id Description UniProt_AApos UniProt_Region UniProt_Site UniProt_Natural_Variations UniProt_Experimental_Info GO_Biological_Process GO_Cellular_Component GO_Molecular_Function COSMIC_overlapping_mutations COSMIC_fusion_genes COSMIC_tissue_types_affected COSMIC_total_alterations_in_gene Tumorscape_Amplification_Peaks Tumorscape_Deletion_Peaks TCGAscape_Amplification_Peaks TCGAscape_Deletion_Peaks DrugBank ref_context gc_content CCLE_ONCOMAP_overlapping_mutations CCLE_ONCOMAP_total_mutations_in_gene CGC_Mutation_Type CGC_Translocation_Partner CGC_Tumor_Types_Somatic CGC_Tumor_Types_Germline CGC_Other_Diseases DNARepairGenes_Role FamilialCancerDatabase_Syndromes MUTSIG_Published_Results OREGANNO_ID OREGANNO_Values t_alt_count t_ref_count validation_alt_allele validation_method validation_status validation_tumor_sample pox qox pox_cutoff isArtifactMode oxoGCut CCDC108 255101 broad.mit.edu 37 2 219886587 219886587 + Silent SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr2:219886587G>A uc002vjl.1 - 17 3129 c.3045C>T c.(3043-3045)gtC>gtT p.V1015V CCDC108_uc002vjm.3_5'Flank NM_194302 NP_919278 Q6ZU64 CC108_HUMAN Homo sapiens coiled-coil domain containing 108 (CCDC108), transcript variant 1, mRNA. 1015 integral to membrane structural molecule activity autonomic_ganglia(1)|breast(1)|cervix(1)|endometrium(4)|kidney(2)|large_intestine(18)|liver(1)|lung(34)|ovary(2)|pancreas(1)|prostate(6)|skin(5)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(1) 80 Renal(207;0.0915) Epithelial(149;1.12e-06)|all cancers(144;0.000196)|LUSC - Lung squamous cell carcinoma(224;0.008)|Lung(261;0.00942) CATTCAGGAGGACAAGGAACC 0.607000 66 137 0 0 1 0 0 PRKD1 5587 broad.mit.edu 37 14 30105538 30105538 + Missense_Mutation SNP T T C TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr14:30105538T>C uc001wqh.3 - 6 1329 c.1148A>G c.(1147-1149)cAa>cGa p.Q383R MIR548AI_uc021rrv.1_Intron NM_002742 NP_002733 Q15139 KPCD1_HUMAN Homo sapiens protein kinase D1 (PRKD1), mRNA. 383 cell proliferation|intracellular signal transduction|sphingolipid metabolic process cytosol|integral to plasma membrane ATP binding|metal ion binding|protein binding|protein kinase C activity NS(1)|breast(2)|endometrium(8)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(21)|lung(32)|ovary(2)|prostate(1)|skin(4)|urinary_tract(2) 78 Hepatocellular(127;0.0604) LUAD - Lung adenocarcinoma(48;0.00527)|Lung(238;0.0252) GBM - Glioblastoma multiforme(265;0.00888) GTCTGGATCTTGCATCTCGCC 0.537000 102 120 0 0 1 0 0 THAP5 168451 broad.mit.edu 37 7 108204990 108204990 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr7:108204990G>A uc003vfm.3 - 2 987 c.833C>T c.(832-834)gCt>gTt p.A278V THAP5_uc003vfl.3_Missense_Mutation_p.A236V NM_001130475 NP_872335 Q7Z6K1 THAP5_HUMAN Homo sapiens THAP domain containing 5 (THAP5), transcript variant 1, mRNA. 278 cell cycle|negative regulation of cell cycle nucleus DNA binding|metal ion binding|protease binding central_nervous_system(1)|kidney(1)|large_intestine(3)|lung(2)|skin(1) 8 AGAATTTTCAGCAGGTACAAA 0.328000 3 33 0 0 1 0 0 ALCAM 214 broad.mit.edu 37 3 105252457 105252457 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr3:105252457G>A uc003dvx.3 + 4 1166 c.470G>A c.(469-471)tGc>tAc p.C157Y ALCAM_uc003dvw.2_Missense_Mutation_p.C157Y|ALCAM_uc003dvy.3_Missense_Mutation_p.C157Y|ALCAM_uc011bhh.1_Missense_Mutation_p.C106Y|ALCAM_uc010hpp.3_5'UTR NM_001627 NP_001618 Q13740 CD166_HUMAN Homo sapiens activated leukocyte cell adhesion molecule (ALCAM), transcript variant 1, mRNA. 157 Ig-like V-type 2. cell adhesion|signal transduction integral to membrane receptor binding breast(1)|cervix(1)|endometrium(2)|kidney(1)|large_intestine(3)|lung(14)|ovary(2)|prostate(1)|skin(2)|urinary_tract(1) 28 TTGGGTGACTGCATTTCAGAA 0.443000 45 49 0 0 1 0 0 PLP1 5354 broad.mit.edu 37 X 103041545 103041545 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chrX:103041545G>A uc010nov.3 + 3 623 c.343G>A c.(343-345)Gca>Aca p.A115T RAB9B_uc004eli.2_Intron|PLP1_uc004elk.3_Missense_Mutation_p.A115T|PLP1_uc004elj.3_Missense_Mutation_p.A115T|PLP1_uc011msf.2_Missense_Mutation_p.A60T|PLP1_uc010now.1_Missense_Mutation_p.A119T|PLP1_uc010nox.3_Missense_Mutation_p.A69T NM_001128834 NP_001122306 P60201 MYPR_HUMAN Homo sapiens proteolipid protein 1 (PLP1), transcript variant 3, mRNA. 115 cell death|synaptic transmission integral to membrane breast(1)|endometrium(1)|large_intestine(2)|lung(10)|ovary(1)|prostate(1)|skin(1) 17 GGGCCTGAGCGCAACGGTAAC 0.582000 4 171 0 0 1 0 0 CKAP2L 150468 broad.mit.edu 37 2 113513632 113513632 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr2:113513632G>A uc002tie.2 - 3 1395 c.1316C>T c.(1315-1317)aCt>aTt p.T439I CKAP2L_uc002tif.2_Missense_Mutation_p.T28I|CKAP2L_uc010yxp.1_Missense_Mutation_p.T274I|CKAP2L_uc010yxq.1_Missense_Mutation_p.T274I NM_152515 NP_689728 Q8IYA6 CKP2L_HUMAN Homo sapiens cytoskeleton associated protein 2-like (CKAP2L), mRNA. 439 centrosome breast(1)|cervix(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(4)|lung(15)|skin(1)|upper_aerodigestive_tract(1) 28 ATCAGCTTGAGTTTTGGGAGC 0.408000 62 70 0 0 1 0 0 LTF 4057 broad.mit.edu 37 3 46484938 46484938 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr3:46484938G>A uc003cpq.3 - 12 1890 c.1649C>T c.(1648-1650)gCt>gTt p.A550V LTF_uc003fzr.3_Missense_Mutation_p.A506V|LTF_uc010hjh.3_Missense_Mutation_p.A548V|LTF_uc003cpr.3_Missense_Mutation_p.A537V NM_002343 NP_001186078 P02788 TRFL_HUMAN Homo sapiens lactotransferrin (LTF), transcript variant 1, mRNA. 550 Transferrin-like 2. cellular iron ion homeostasis|defense response to bacterium|humoral immune response|iron ion transport extracellular region|stored secretory granule ferric iron binding|heparin binding|protein binding|serine-type endopeptidase activity NS(1)|breast(3)|central_nervous_system(3)|endometrium(4)|kidney(3)|large_intestine(5)|lung(13)|ovary(1)|prostate(1)|skin(4)|upper_aerodigestive_tract(2) 40 all cancers(1;7.55e-14)|GBM - Glioblastoma multiforme(1;2.1e-09)|Epithelial(1;9.25e-07)|Colorectal(1;3.81e-05)|BRCA - Breast invasive adenocarcinoma(193;0.00129)|COAD - Colon adenocarcinoma(1;0.00308)|KIRC - Kidney renal clear cell carcinoma(197;0.0205)|Kidney(197;0.0242)|OV - Ovarian serous cystadenocarcinoma(275;0.089) Pefloxacin(DB00487) TCACCGGAAAGCCCCAGTGTA 0.532000 80 108 0 0 1 0 0 ATP2B4 493 broad.mit.edu 37 1 203680123 203680123 + Missense_Mutation SNP A A G TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr1:203680123A>G uc001gzw.3 + 11 2815 c.1918A>G c.(1918-1920)Ata>Gta p.I640V ATP2B4_uc001gzv.3_Missense_Mutation_p.I640V|ATP2B4_uc009xaq.3_Missense_Mutation_p.I640V NM_001684 NP_001675 P23634 AT2B4_HUMAN Homo sapiens ATPase, Ca++ transporting, plasma membrane 4 (ATP2B4), transcript variant 2, mRNA. 640 ATP biosynthetic process|platelet activation integral to plasma membrane ATP binding|calcium-transporting ATPase activity|calmodulin binding|metal ion binding|protein binding NS(1)|breast(1)|central_nervous_system(2)|cervix(2)|endometrium(5)|kidney(2)|large_intestine(10)|lung(20)|ovary(2)|prostate(6)|skin(1)|stomach(1)|urinary_tract(3) 56 all_cancers(21;0.071)|all_epithelial(62;0.228) BRCA - Breast invasive adenocarcinoma(75;0.109) GACTATCTGCATAGCTTACCG 0.532000 42 82 0 0 1 0 0 LDHA 3939 broad.mit.edu 37 11 18427040 18427040 + Missense_Mutation SNP T T C TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr11:18427040T>C uc010rdd.2 + 6 1124 c.842T>C c.(841-843)aTt>aCt p.I281T LDHA_uc001mok.3_Missense_Mutation_p.I252T|LDHA_uc009yho.2_Missense_Mutation_p.I79T|LDHA_uc001mol.3_Intron|LDHA_uc010rdc.1_Missense_Mutation_p.I194T|LDHA_uc021qep.1_Intron NM_001165414 NP_005557 P00338 LDHA_HUMAN Homo sapiens lactate dehydrogenase A (LDHA), transcript variant 3, mRNA. 252 glycolysis|pyruvate metabolic process cytosol L-lactate dehydrogenase activity|protein binding p.Y281C(1) central_nervous_system(3)|endometrium(1)|large_intestine(4)|lung(4) 12 NADH(DB00157) TCCTGGGCTATTGGACTCTCT 0.443000 4 72 0 0 1 0 0 TRIO 7204 broad.mit.edu 37 5 14297305 14297305 + Missense_Mutation SNP C C T TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr5:14297305C>T uc003jff.3 + 6 1307 c.1301C>T c.(1300-1302)gCg>gTg p.A434V TRIO_uc003jfg.3_Non-coding_Transcript|TRIO_uc011cna.1_Missense_Mutation_p.A385V|TRIO_uc003jfh.1_Missense_Mutation_p.A83V NM_007118 NP_009049 O75962 TRIO_HUMAN Homo sapiens triple functional domain (PTPRF interacting) (TRIO), mRNA. 434 apoptosis|axon guidance|induction of apoptosis by extracellular signals|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction|transmembrane receptor protein tyrosine phosphatase signaling pathway cytosol ATP binding|Rho guanyl-nucleotide exchange factor activity|protein serine/threonine kinase activity NS(2)|breast(6)|central_nervous_system(4)|endometrium(16)|haematopoietic_and_lymphoid_tissue(1)|kidney(7)|large_intestine(21)|lung(34)|ovary(4)|prostate(2)|skin(11)|stomach(3)|upper_aerodigestive_tract(3)|urinary_tract(4) 118 Lung NSC(4;0.000742) AAGGCGTTTGCGGCAGCCCTG 0.602000 3 46 0 0 1 0 0 SRSF5 6430 broad.mit.edu 37 14 70237718 70237718 + Silent SNP T T G TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr14:70237718T>G uc001xll.3 + 7 1898 c.447T>G c.(445-447)gtT>gtG p.V149V SRSF5_uc001xlo.3_Silent_p.V149V|SRSF5_uc001xlp.3_Silent_p.V149V NM_006925 NP_008856 Q13243 SRSF5_HUMAN Homo sapiens serine/arginine-rich splicing factor 5 (SRSF5), transcript variant 2, mRNA. 149 RRM 2. mRNA 3'-end processing|mRNA export from nucleus|mRNA splice site selection|termination of RNA polymerase II transcription nuclear speck RNA binding|nucleotide binding|protein binding large_intestine(1)|liver(1) 2 TTAGGGTGGTTGAGTTTGCCT 0.358000 6 24 0 0 1 0 0 PTPRS 5802 broad.mit.edu 37 19 5206842 5206842 + Missense_Mutation SNP C C G TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr19:5206842C>G uc002mbv.3 - 37 6024 c.5790G>C c.(5788-5790)caG>caC p.Q1930H PTPRS_uc002mbu.1_Intron|PTPRS_uc010xin.2_Missense_Mutation_p.Q1472H|PTPRS_uc002mbw.3_Missense_Mutation_p.Q1892H|PTPRS_uc002mbx.3_Missense_Mutation_p.Q1487H|PTPRS_uc002mby.3_Missense_Mutation_p.Q1483H NM_002850 NP_002841 Q13332 PTPRS_HUMAN Homo sapiens protein tyrosine phosphatase, receptor type, S (PTPRS), transcript variant 1, mRNA. 1930 Tyrosine-protein phosphatase 2. cell adhesion integral to plasma membrane protein binding|transmembrane receptor protein tyrosine phosphatase activity NS(1)|biliary_tract(1)|central_nervous_system(1)|endometrium(12)|haematopoietic_and_lymphoid_tissue(1)|kidney(3)|large_intestine(12)|liver(1)|lung(9)|ovary(4)|prostate(1)|skin(12)|stomach(2)|upper_aerodigestive_tract(1) 61 UCEC - Uterine corpus endometrioid carcinoma (162;6.64e-05)|BRCA - Breast invasive adenocarcinoma(158;0.0321)|Lung(535;0.182) GGTAACAGAACTGGTACTCAT 0.612000 7 99 0 0 1 0 0 ZNF713 349075 broad.mit.edu 37 7 56006963 56006963 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr7:56006963G>A uc003tra.2 + 6 1403 c.596G>A c.(595-597)aGa>aAa p.R199K ZNF713_uc003trc.1_Missense_Mutation_p.R186K NM_182633 NP_872439 Q8N859 ZN713_HUMAN Homo sapiens zinc finger protein 713 (ZNF713), mRNA. 186 regulation of transcription, DNA-dependent|transcription, DNA-dependent nucleus DNA binding|zinc ion binding breast(2)|endometrium(1)|kidney(1)|large_intestine(4)|lung(10)|ovary(2)|prostate(2)|upper_aerodigestive_tract(2)|urinary_tract(1) 25 Breast(14;0.214) Lung(13;0.00024)|LUSC - Lung squamous cell carcinoma(13;0.00099) ATGCAGCAGAGAATTCCTTCC 0.368000 13 28 0 0 1 0 0 CATSPERB 79820 broad.mit.edu 37 14 92088170 92088170 + Missense_Mutation SNP G G A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr14:92088170G>A uc001xzs.1 - 18 2182 c.2042C>T c.(2041-2043)gCt>gTt p.A681V CATSPERB_uc010aub.1_Missense_Mutation_p.A203V NM_024764 NP_079040 Q9H7T0 CTSRB_HUMAN Homo sapiens cation channel, sperm-associated, beta (CATSPERB), mRNA. 681 cell differentiation|multicellular organismal development|spermatogenesis integral to membrane NS(1)|breast(4)|central_nervous_system(1)|kidney(3)|large_intestine(15)|liver(1)|lung(12)|ovary(2)|pancreas(1)|prostate(3)|skin(9)|urinary_tract(2) 54 all_cancers(154;0.0663)|all_epithelial(191;0.236) AGGCATGGTAGCAATGGCTAA 0.393000 3 47 0 0 1 0 0 MYH2 4620 broad.mit.edu 37 17 10432293 10432293 + Missense_Mutation SNP C C A TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr17:10432293C>A uc010coi.3 - 26 3586 c.3458G>T c.(3457-3459)aGc>aTc p.S1153I AK097500_uc002gml.1_Intron|MYH2_uc002gmp.4_Missense_Mutation_p.S1153I|MYH2_uc010coj.3_Intron NM_001100112 NP_060004 Q9UKX2 MYH2_HUMAN Homo sapiens myosin, heavy chain 2, skeletal muscle, adult (MYH2), transcript variant 2, mRNA. 1153 muscle filament sliding muscle myosin complex|myosin filament|sarcomere ATP binding|actin binding|calmodulin binding|microfilament motor activity|structural constituent of muscle NS(1)|biliary_tract(1)|breast(9)|central_nervous_system(1)|endometrium(13)|haematopoietic_and_lymphoid_tissue(1)|kidney(8)|large_intestine(16)|lung(99)|ovary(6)|pancreas(4)|prostate(3)|skin(8)|upper_aerodigestive_tract(2)|urinary_tract(4) 176 CAGCCTCTCGCTGATCTCCTC 0.617000 90 96 0 0 1 0 0 TSFM 10102 broad.mit.edu 37 12 58176601 58176601 + Missense_Mutation SNP C C T TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr12:58176601C>T uc001sqh.3 + 0 74 c.17C>T c.(16-18)tCg>tTg p.S6L TSFM_uc021qzq.1_Missense_Mutation_p.S6L|TSFM_uc001sqi.3_Missense_Mutation_p.S6L|TSFM_uc010ssf.2_Missense_Mutation_p.S6L|TSFM_uc010sse.2_5'UTR NM_001172696 NP_001166167 P43897 EFTS_HUMAN Homo sapiens Ts translation elongation factor, mitochondrial (TSFM), nuclear gene encoding mitochondrial protein, transcript variant 1, mRNA. 6 regulation of transcription elongation, DNA-dependent mitochondrion|nucleus translation elongation factor activity endometrium(1)|kidney(1)|large_intestine(5)|prostate(1) 8 all_cancers(7;6.31e-80)|Glioma(12;6.95e-05)|all_neural(12;0.00016)|Melanoma(17;0.122) CTGCTGCGGTCGCTGCGCGTG 0.652000 OREG0021954 type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip) 4 9 0 0 1 0 0 GNL1 2794 broad.mit.edu 37 6 30513930 30513931 + Frame_Shift_Del DEL AT AT - TCGA-J8-A3O1-01A-11D-A21A-08 TCGA-J8-A3O1-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx 1471f233-85c1-4689-853a-01947d5ba299 d48f2242-1f17-4fef-a647-c19839582493 g.chr6:30513930_30513931delAT uc003nqh.3 - 11 3133_3134 c.1742_1743delAT c.(1741-1743)gatfs p.D581fs GNL1_uc011dmi.2_Frame_Shift_Del_p.D378fs|GNL1_uc011dmj.2_Frame_Shift_Del_p.D579fs|GNL1_uc011dmk.2_Frame_Shift_Del_p.D236fs NM_005275 NP_005266 P36915 GNL1_HUMAN Homo sapiens guanine nucleotide binding protein-like 1 (GNL1), mRNA. 581 Asp/Glu-rich (highly acidic). T cell mediated immunity|response to DNA damage stimulus|signal transduction extracellular space|intracellular GTP binding|structural molecule activity cervix(2)|endometrium(4)|large_intestine(1)|lung(10)|ovary(4)|prostate(2)|skin(1)|upper_aerodigestive_tract(1) 25 GGGTctcctcatccccttctcc 0.639 2 4 --- --- --- ---