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 VGLL1 51442 broad.mit.edu 37 X 135631112 135631112 + Silent SNP C C T TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chrX:135631112C>T ENST00000370634.3 + 3 749 c.579C>T c.(577-579)ggC>ggT p.G193G NM_016267.3 NP_057351.1 Q99990 VGLL1_HUMAN vestigial like 1 (Drosophila) 193 regulation of transcription, DNA-dependent|transcription, DNA-dependent nucleus transcription coactivator activity breast(1)|endometrium(1)|kidney(1)|large_intestine(7)|lung(7)|ovary(1)|stomach(1)|upper_aerodigestive_tract(1) 20 Acute lymphoblastic leukemia(192;0.000127) GCAACCCTGGCCAGATAGCTG 0.562000 4 172 0 0 0.009096 0 0 COX10-AS1 0 broad.mit.edu 37 17 13928289 13928289 + RNA SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr17:13928289G>A ENST00000602743.1 - 0 224 CGGAGCCAGAGCCAGCATGGG 0.592000 3 5 0 0 0.004672 0 0 DENND4C 55667 broad.mit.edu 37 9 19360258 19360258 + Missense_Mutation SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr9:19360258G>A ENST00000307015.9 + 25 4493 c.2741G>A c.(2740-2742)aGa>aAa p.R914K DENND4C_ENST00000540671.1_Missense_Mutation_p.R771K|DENND4C_ENST00000434457.2_Missense_Mutation_p.R1726K|DENND4C_ENST00000602925.1_Missense_Mutation_p.R1677K|DENND4C_ENST00000380432.2_Missense_Mutation_p.R1441K Q5VZ89 DEN4C_HUMAN DENN/MADD domain containing 4C 1441 integral to membrane breast(1)|endometrium(8)|kidney(1)|large_intestine(7)|liver(2)|lung(13)|ovary(1)|prostate(2)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1) 40 TTAGGAAAAAGACCCAATCCT 0.363000 5 149 0 0 0.001984 0 0 ARAP1 116985 broad.mit.edu 37 11 72406076 72406076 + Missense_Mutation SNP T T C TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr11:72406076T>C ENST00000359373.5 - 27 4494 c.3643A>G c.(3643-3645)Agg>Ggg p.R1215G ARAP1_ENST00000429686.1_Missense_Mutation_p.R909G|ARAP1_ENST00000393609.3_Missense_Mutation_p.R1215G|ARAP1_ENST00000455638.2_Missense_Mutation_p.R1215G|ARAP1_ENST00000393605.3_Missense_Mutation_p.R975G|ARAP1_ENST00000495878.1_5'UTR|ARAP1_ENST00000426523.1_Missense_Mutation_p.R970G|ARAP1_ENST00000334211.8_Missense_Mutation_p.R970G Q96P48 ARAP1_HUMAN ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 1215 Ras-associating. actin filament reorganization involved in cell cycle|negative regulation of stress fiber assembly|positive regulation of Cdc42 GTPase activity|positive regulation of filopodium assembly|regulation of ARF GTPase activity|regulation of cell shape|regulation of cellular component movement|small GTPase mediated signal transduction cytosol|Golgi cisterna membrane|plasma membrane ARF GTPase activator activity|phosphatidylinositol-3,4,5-trisphosphate binding|protein binding|Rho GTPase activator activity|zinc ion binding p.R975G(1)|p.R1215G(1) cervix(2)|endometrium(2)|large_intestine(10)|lung(8)|ovary(1)|skin(3)|urinary_tract(1) 27 TCCTTCTCCCTGATGCCCACG 0.587000 3 31 0 0 0.004672 0 0 SETD4 54093 broad.mit.edu 37 21 37420619 37420619 + Missense_Mutation SNP C C T TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr21:37420619C>T ENST00000399215.1 - 4 1655 c.283G>A c.(283-285)Gca>Aca p.A95T SETD4_ENST00000481477.1_Intron|SETD4_ENST00000399201.1_Missense_Mutation_p.A71T|SETD4_ENST00000399207.1_Missense_Mutation_p.A95T|SETD4_ENST00000399212.1_Missense_Mutation_p.A71T|SETD4_ENST00000332131.4_Missense_Mutation_p.A95T|SETD4_ENST00000399205.1_Missense_Mutation_p.A71T|SETD4_ENST00000399208.2_Missense_Mutation_p.A95T Q9NVD3 SETD4_HUMAN SET domain containing 4 95 SET. autonomic_ganglia(1)|kidney(2)|large_intestine(4)|lung(6)|ovary(1)|prostate(1) 15 GTAATGTATGCCCCTAAGTAG 0.448000 5 287 0 0 0.001984 0 0 HSD3B2 3284 broad.mit.edu 37 1 119965210 119965210 + Silent SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr1:119965210G>A ENST00000543831.1 + 4 1335 c.1086G>A c.(1084-1086)cgG>cgA p.R362R HSD3B2_ENST00000369416.3_Silent_p.R362R NM_001166120.1 NP_001159592.1 P26439 3BHS2_HUMAN hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 362 androgen biosynthetic process|glucocorticoid biosynthetic process|mineralocorticoid biosynthetic process integral to membrane|microsome|mitochondrial inner membrane|mitochondrial intermembrane space|smooth endoplasmic reticulum membrane 3-beta-hydroxy-delta5-steroid dehydrogenase activity|binding|steroid delta-isomerase activity p.R362R(1) breast(1)|endometrium(2)|kidney(1)|large_intestine(1)|lung(19)|ovary(2)|skin(1) 27 all_neural(166;0.187) all_lung(203;1.06e-06)|Lung NSC(69;7.5e-06)|all_epithelial(167;0.000284) Lung(183;0.015)|LUSC - Lung squamous cell carcinoma(189;0.0836) NADH(DB00157)|Trilostane(DB01108) TTGTGGACCGGCACAAGGAGA 0.512000 4 65 0 0 0.000602 0 0 MAST1 22983 broad.mit.edu 37 19 12951846 12951846 + Missense_Mutation SNP A A C TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr19:12951846A>C ENST00000251472.4 + 3 253 c.214A>C c.(214-216)Acc>Ccc p.T72P MAST1_ENST00000591495.1_Missense_Mutation_p.T68P NM_014975.2 NP_055790.1 Q9Y2H9 MAST1_HUMAN microtubule associated serine/threonine kinase 1 72 cytoskeleton organization|intracellular protein kinase cascade cytoplasm|cytoskeleton|plasma membrane ATP binding|magnesium ion binding|protein serine/threonine kinase activity NS(1)|cervix(2)|endometrium(9)|haematopoietic_and_lymphoid_tissue(2)|large_intestine(9)|lung(20)|ovary(5)|prostate(5)|skin(3) 56 CTCCCCCAACACCCCCGCCCA 0.642000 8 82 0 0 0.003163 0 0 MCF2L 23263 broad.mit.edu 37 13 113740522 113740522 + Missense_Mutation SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr13:113740522G>A ENST00000397030.1 + 21 2468 c.2431G>A c.(2431-2433)Gtg>Atg p.V811M MCF2L_ENST00000535094.2_Missense_Mutation_p.V778M|MCF2L_ENST00000375597.4_Missense_Mutation_p.V776M|MCF2L_ENST00000375604.2_Missense_Mutation_p.V835M|MCF2L_ENST00000375608.3_Missense_Mutation_p.V808M|MCF2L_ENST00000375601.3_Missense_Mutation_p.V782M|MCF2L_ENST00000423482.2_Missense_Mutation_p.V776M|MCF2L_ENST00000442652.2_Missense_Mutation_p.V808M|MCF2L_ENST00000421756.1_Missense_Mutation_p.V782M|MCF2L_ENST00000434480.2_Missense_Mutation_p.V784M O15068 MCF2L_HUMAN MCF.2 cell line derived transforming sequence-like 808 DH. apoptosis|induction of apoptosis by extracellular signals|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction cytosol|plasma membrane Rho guanyl-nucleotide exchange factor activity kidney(1)|large_intestine(5)|ovary(1)|stomach(1) 8 all_lung(23;0.000374)|Lung NSC(43;0.0107)|Lung SC(71;0.0753)|all_neural(89;0.0804)|Hepatocellular(20;0.0877)|Medulloblastoma(90;0.163) all_cancers(25;0.118)|all_lung(25;0.0368)|all_epithelial(44;0.0396)|Lung NSC(25;0.129)|Breast(118;0.188) CCTGAAGGCCGTGAACGACTC 0.622000 3 43 0 0 0.004672 0 0 HSD17B7P2 0 broad.mit.edu 37 10 38654432 38654432 + RNA SNP A A G rs2257765 TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr10:38654432A>G ENST00000494540.1 + 0 599 NR_003086.1 TCATCTCGCAATGCAAGGAAA 0.453000 3 60 0 0 0.004672 0 0 RP9 6100 broad.mit.edu 37 7 33139017 33139017 + Missense_Mutation SNP G G C TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr7:33139017G>C ENST00000297157.3 - 3 232 c.215C>G c.(214-216)cCa>cGa p.P72R NM_203288.1 NP_976033.1 Q8TA86 RP9_HUMAN retinitis pigmentosa 9 (autosomal dominant) 72 PIM1-binding (By similarity). RNA splicing nucleus nucleic acid binding|protein binding|zinc ion binding p.P72R(2) large_intestine(3)|lung(3)|urinary_tract(1) 7 GBM - Glioblastoma multiforme(11;0.0403) TGGTACATCTGGTATGCAATC 0.483000 5 80 0 0 0.000602 0 0 CDC40 51362 broad.mit.edu 37 6 110528751 110528751 + Missense_Mutation SNP C C A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr6:110528751C>A ENST00000368932.1 + 5 550 c.449C>A c.(448-450)gCt>gAt p.A150D CDC40_ENST00000368933.1_Missense_Mutation_p.A150D|CDC40_ENST00000307731.1_Missense_Mutation_p.A150D|CDC40_ENST00000368930.1_Missense_Mutation_p.A150D O60508 PRP17_HUMAN cell division cycle 40 150 mRNA 3'-end processing|mRNA export from nucleus|termination of RNA polymerase II transcription catalytic step 2 spliceosome|nucleoplasm p.A150D(1) breast(1)|cervix(1)|endometrium(1)|kidney(2)|large_intestine(4)|lung(7)|prostate(1)|skin(1) 18 all_cancers(87;6.23e-06)|Acute lymphoblastic leukemia(125;2.66e-08)|all_hematologic(75;1.13e-06)|all_epithelial(87;0.00159)|Colorectal(196;0.0488) Epithelial(106;0.0221)|all cancers(137;0.0314)|OV - Ovarian serous cystadenocarcinoma(136;0.034) CAAGTGTCTGCTAAATATATT 0.269000 5 135 0.00116845 0.00211781 0.001168 1 0 BRAF 673 broad.mit.edu 37 7 140453136 140453136 + Missense_Mutation SNP A A T rs121913377 TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr7:140453136A>T ENST00000288602.6 - 15 1859 c.1799T>A c.(1798-1800)gTg>gAg p.V600E NM_004333.4 NP_004324.2 P15056 BRAF_HUMAN v-raf murine sarcoma viral oncogene homolog B 600 Protein kinase. V -> D (in a melanoma cell line; requires 2 nucleotide substitutions).|V -> E (in sarcoma, colorectal adenocarcinoma, metastatic melanoma, ovarian serous carcinoma, pilocytic astrocytoma; somatic mutation; most common mutation; constitutive and elevated kinase activity; efficiently induces cell transformation; suppression of mutation in melanoma causes growth arrest and promotes apoptosis). activation of MAPKK activity|anti-apoptosis|nerve growth factor receptor signaling pathway|organ morphogenesis|positive regulation of peptidyl-serine phosphorylation|small GTPase mediated signal transduction|synaptic transmission cytosol|nucleus|plasma membrane ATP binding|metal ion binding p.V600E(15453)|p.V600K(252)|p.V600R(44)|p.V600D(16)|p.V600A(12)|p.V600_K601>E(12)|p.V600G(11)|p.T599_R603>I(2)|p.V600Q(2)|p.V600_S605>EK(1)|p.V600_S605>DV(1)|p.V600_S605>D(1)|p.T599_V600insDFGLAT(1) SLC45A3/BRAF(2)|AGTRAP/BRAF(2)|FAM131B_ENST00000443739/BRAF(7)|AKAP9_ENST00000356239/BRAF(10)|KIAA1549/BRAF(703)|FCHSD1/BRAF(2) NS(588)|adrenal_gland(3)|autonomic_ganglia(3)|biliary_tract(29)|bone(7)|breast(21)|central_nervous_system(99)|cervix(6)|endometrium(33)|eye(72)|gastrointestinal_tract_(site_indeterminate)(2)|genital_tract(4)|haematopoietic_and_lymphoid_tissue(436)|kidney(3)|large_intestine(6953)|liver(17)|lung(192)|oesophagus(4)|ovary(275)|pancreas(15)|pituitary(1)|prostate(25)|salivary_gland(1)|skin(6285)|small_intestine(12)|soft_tissue(40)|stomach(11)|testis(7)|thyroid(12220)|upper_aerodigestive_tract(13)|urinary_tract(3) 27380 Melanoma(164;0.00956) Sorafenib(DB00398) TCGAGATTTCACTGTAGCTAG 0.368000 V600D(K029AX_SKIN)|V600D(WM115_SKIN)|V600D(WM2664_SKIN)|V600E(8505C_THYROID)|V600E(A101D_SKIN)|V600E(A2058_SKIN)|V600E(A375_SKIN)|V600E(A673_BONE)|V600E(AM38_CENTRAL_NERVOUS_SYSTEM)|V600E(BCPAP_THYROID)|V600E(BHT101_THYROID)|V600E(BT474_BREAST)|V600E(C32_SKIN)|V600E(CL34_LARGE_INTESTINE)|V600E(COLO205_LARGE_INTESTINE)|V600E(COLO679_SKIN)|V600E(COLO741_SKIN)|V600E(COLO783_SKIN)|V600E(COLO800_SKIN)|V600E(COLO818_SKIN)|V600E(COLO829_SKIN)|V600E(COLO849_SKIN)|V600E(DBTRG05MG_CENTRAL_NERVOUS_SYSTEM)|V600E(DU4475_BREAST)|V600E(ES2_OVARY)|V600E(G361_SKIN)|V600E(GCT_SOFT_TISSUE)|V600E(HS294T_SKIN)|V600E(HS695T_SKIN)|V600E(HS939T_SKIN)|V600E(IGR1_SKIN)|V600E(IGR37_SKIN)|V600E(IGR39_SKIN)|V600E(K029AX_SKIN)|V600E(KG1C_CENTRAL_NERVOUS_SYSTEM)|V600E(LOXIMVI_SKIN)|V600E(MALME3M_SKIN)|V600E(MELHO_SKIN)|V600E(OUMS23_LARGE_INTESTINE)|V600E(RKO_LARGE_INTESTINE)|V600E(RPMI7951_SKIN)|V600E(RVH421_SKIN)|V600E(SH4_SKIN)|V600E(SIGM5_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE)|V600E(SKHEP1_LIVER)|V600E(SKMEL24_SKIN)|V600E(SKMEL28_SKIN)|V600E(SKMEL5_SKIN)|V600E(SW1417_LARGE_INTESTINE)|V600E(UACC257_SKIN)|V600E(UACC62_SKIN)|V600E(WM793_SKIN)|V600E(WM88_SKIN)|V600E(WM983B_SKIN) 61 """Mis, T, O""" """AKAP9, KIAA1549""" """melanoma, colorectal, papillary thyroid, borderline ov, Non small-cell lung cancer (NSCLC), cholangiocarcinoma, pilocytic astrocytoma""" Cardio-facio-cutaneous syndrome Cardiofaciocutaneous syndrome 18 56 0 0 0.010504 0 0 NUDT5 11164 broad.mit.edu 37 10 12215790 12215790 + Silent SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr10:12215790G>A ENST00000491614.1 - 6 707 c.312C>T c.(310-312)acC>acT p.T104T NUDT5_ENST00000378937.3_Silent_p.T117T|NUDT5_ENST00000378940.3_Silent_p.T104T|NUDT5_ENST00000378952.3_5'UTR|NUDT5_ENST00000378927.3_Silent_p.T104T|NUDT5_ENST00000537776.1_Silent_p.T104T Q9UKK9 NUDT5_HUMAN nudix (nucleoside diphosphate linked moiety X)-type motif 5 104 Nudix hydrolase. D-ribose catabolic process|ribonucleoside diphosphate catabolic process intracellular ADP-ribose diphosphatase activity|magnesium ion binding breast(1)|large_intestine(1)|lung(4)|ovary(1)|pancreas(1) 8 Renal(717;0.228) CTGCTTCTGGGGTTTCACCAT 0.458000 73 148 0 0 0.014410 0 0 TSPAN4 0 broad.mit.edu 37 11 865530 865530 + Silent SNP G G A TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr11:865530G>A ENST00000397404.1 + 6 607 c.348G>A c.(346-348)caG>caA p.Q116Q TSPAN4_ENST00000397397.2_Silent_p.Q116Q|TSPAN4_ENST00000346501.4_Intron|TSPAN4_ENST00000397396.1_Silent_p.Q52Q|TSPAN4_ENST00000397408.1_Silent_p.Q116Q|TSPAN4_ENST00000397411.2_Silent_p.Q116Q|TSPAN4_ENST00000525201.1_Silent_p.Q52Q|TSPAN4_ENST00000409531.1_Silent_p.Q135Q|TSPAN4_ENST00000397406.1_Silent_p.Q116Q|TSPAN4_ENST00000409543.2_Silent_p.Q116Q NM_001025237.1 NP_001020408.1 O14817 TSN4_HUMAN tetraspanin 4 116 protein complex assembly integral to plasma membrane breast(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1) 3 all_cancers(49;2.64e-08)|all_epithelial(84;4.17e-05)|Breast(177;0.000307)|Ovarian(85;0.000953)|Medulloblastoma(188;0.0109)|all_neural(188;0.0299)|Lung NSC(207;0.191)|all_lung(207;0.24) all cancers(45;4.32e-25)|Epithelial(43;3.29e-24)|BRCA - Breast invasive adenocarcinoma(625;4.23e-05)|Lung(200;0.0576)|LUSC - Lung squamous cell carcinoma(625;0.0703) GGTATGCCCAGCAAGACCTGA 0.667000 3 27 0 0 0.004672 0 0 KMT2C 58508 broad.mit.edu 37 7 151970890 151970891 + Frame_Shift_Ins INS - - T TCGA-DJ-A2PS-01A-11D-A18F-08 TCGA-DJ-A2PS-10A-01D-A18F-08 Untested Somatic Phase_I WXS none Illumina GAIIx 96c450fe-4e43-43b3-9adc-6549c6fff902 dd8e6cf7-7163-4b83-a429-6f19ce5690b3 g.chr7:151970890_151970891insT ENST00000355193.2 - 7 1129_1130 c.911_912insA c.(910-912)catfs p.H304fs KMT2C_ENST00000262189.6_Frame_Shift_Ins_p.H304fs lysine (K)-specific methyltransferase 2C AATGATACATCTGGGTACATTT 0.436 8 166 --- --- --- ---