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 ITGAM 3684 broad.mit.edu 37 16 31283280 31283280 + Missense_Mutation SNP G G A TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr16:31283280G>A uc002ebr.3 + 6 769 c.671G>A c.(670-672)cGg>cAg p.R224Q ITGAM_uc002ebq.3_Missense_Mutation_p.R224Q NM_001145808 NP_001139280 P11215 ITAM_HUMAN Homo sapiens integrin, alpha M (complement component 3 receptor 3 subunit) (ITGAM), transcript variant 1, mRNA. 224 VWFA. blood coagulation|cell adhesion|integrin-mediated signaling pathway|leukocyte migration integrin complex glycoprotein binding|receptor activity p.G223W(1) endometrium(7)|kidney(1)|large_intestine(10)|lung(32)|ovary(1)|prostate(4)|skin(1) 56 CTGCTTGGGCGGACACACACG 0.512000 4 142 0 0 1 0 0 ZBTB22 9278 broad.mit.edu 37 6 33283858 33283858 + Missense_Mutation SNP G G T TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr6:33283858G>T uc003oeb.3 - 1 988 c.836C>A c.(835-837)gCt>gAt p.A279D TAPBP_uc003odx.2_5'Flank|TAPBP_uc010jut.2_5'Flank|TAPBP_uc003odz.3_5'Flank|TAPBP_uc003ody.3_5'Flank|TAPBP_uc011drc.2_5'Flank|ZBTB22_uc010juu.3_Missense_Mutation_p.A279D|ZBTB22_uc021ywm.1_Missense_Mutation_p.A279D NM_005453 NP_005444 O15209 ZBT22_HUMAN Homo sapiens zinc finger and BTB domain containing 22 (ZBTB22), transcript variant 1, mRNA. 279 regulation of transcription, DNA-dependent|transcription, DNA-dependent nucleus DNA binding|zinc ion binding breast(1)|central_nervous_system(1)|endometrium(3)|large_intestine(1)|lung(9)|ovary(2)|prostate(1)|urinary_tract(3) 21 CCGGAGCCCAGCCCCAGGAAC 0.617000 24 59 0 0 1 0 0 HGD 3081 broad.mit.edu 37 3 120389285 120389285 + Missense_Mutation SNP C C G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr3:120389285C>G uc003edw.3 - 3 731 c.271G>C c.(271-273)Gat>Cat p.D91H NM_000187 NP_000178 Q93099 HGD_HUMAN Homo sapiens homogentisate 1,2-dioxygenase (HGD), mRNA. 91 L-phenylalanine catabolic process|tyrosine catabolic process cytosol homogentisate 1,2-dioxygenase activity|metal ion binding cervix(1)|endometrium(4)|kidney(2)|large_intestine(3)|lung(11)|ovary(1)|prostate(1)|skin(2) 25 GBM - Glioblastoma multiforme(114;0.158) TGGTTAGGATCAGGATCAACT 0.418000 26 72 0 0 1 0 0 TJP1 7082 broad.mit.edu 37 15 30012630 30012630 + Missense_Mutation SNP A A C TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr15:30012630A>C uc010azl.3 - 17 2668 c.2659T>G c.(2659-2661)Tca>Gca p.S887A TJP1_uc001zcq.3_Missense_Mutation_p.S903A|TJP1_uc001zcr.3_Missense_Mutation_p.S899A|TJP1_uc001zcs.3_Missense_Mutation_p.S899A NM_003257 NP_003248 Q07157 ZO1_HUMAN Homo sapiens tight junction protein 1 (zona occludens 1) (TJP1), transcript variant 1, mRNA. 899 cell-cell junction assembly|cellular component disassembly involved in apoptosis Golgi apparatus|basolateral plasma membrane|cell-cell adherens junction|tight junction p.S886P(1) breast(4)|central_nervous_system(2)|endometrium(8)|kidney(3)|large_intestine(12)|liver(1)|lung(29)|ovary(4)|pancreas(1)|prostate(3)|urinary_tract(1) 68 all_lung(180;7.48e-11)|Breast(32;0.000153) all cancers(64;3.29e-10)|Epithelial(43;5.34e-09)|BRCA - Breast invasive adenocarcinoma(123;0.0034)|GBM - Glioblastoma multiforme(186;0.0139)|Lung(196;0.186) GCTTGTGGTGAGTAAGGAGGA 0.483000 28 78 0 0 1 0 0 SMC3 9126 broad.mit.edu 37 10 112335096 112335096 + Missense_Mutation SNP A A G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr10:112335096A>G uc001kze.3 + 3 259 c.133A>G c.(133-135)Att>Gtt p.I45V NM_005445 NP_005436 Q9UQE7 SMC3_HUMAN Homo sapiens structural maintenance of chromosomes 3 (SMC3), mRNA. 45 DNA mediated transformation|DNA repair|cell division|meiosis|mitotic metaphase/anaphase transition|mitotic prometaphase|mitotic spindle organization|negative regulation of DNA endoreduplication|signal transduction|sister chromatid cohesion basement membrane|chromatin|chromosome, centromeric region|cytoplasm|meiotic cohesin complex|nuclear matrix|nucleoplasm|spindle pole ATP binding|dynein binding|microtubule motor activity|protein heterodimerization activity p.A44V(1) NS(1)|breast(1)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(3)|kidney(7)|large_intestine(5)|lung(13)|ovary(1)|skin(2)|upper_aerodigestive_tract(2)|urinary_tract(1) 39 Breast(234;0.0848)|Lung NSC(174;0.238) Epithelial(162;0.00206)|all cancers(201;0.0227)|BRCA - Breast invasive adenocarcinoma(275;0.127) ATTTCCAGCAATTCAGTTTGT 0.338000 17 26 0 0 1 0 0 G6PD 2539 broad.mit.edu 37 X 153763439 153763439 + Silent SNP G G C TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chrX:153763439G>C uc004flx.1 - 4 667 c.519C>G c.(517-519)ccC>ccG p.P173P G6PD_uc004fly.1_Silent_p.P143P NM_000402 NP_001035810 P11413 G6PD_HUMAN Homo sapiens glucose-6-phosphate dehydrogenase (G6PD), transcript variant 1, mRNA. 143 cellular response to oxidative stress|cholesterol biosynthetic process|cytokine production|erythrocyte maturation|glucose 6-phosphate metabolic process|glutathione metabolic process|negative regulation of protein glutathionylation|pentose-phosphate shunt, oxidative branch|ribose phosphate biosynthetic process centrosome|cytosol|internal side of plasma membrane|intracellular membrane-bounded organelle NADP binding|glucose binding|glucose-6-phosphate dehydrogenase activity|protein homodimerization activity breast(2)|central_nervous_system(1)|endometrium(4)|kidney(1)|large_intestine(3)|lung(3)|ovary(4) 18 all_cancers(53;5.05e-16)|all_epithelial(53;1.87e-10)|all_lung(58;1.84e-07)|Lung NSC(58;5.84e-07)|all_hematologic(71;2.45e-06)|Acute lymphoblastic leukemia(192;6.56e-05)|Breast(217;0.176) AGACGGTCGGGGGCAAGGCCA 0.627000 4 170 0 0 1 0 0 COL4A2 1284 broad.mit.edu 37 13 111099179 111099179 + Missense_Mutation SNP C C T TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr13:111099179C>T uc001vqx.3 + 17 1335 c.1046C>T c.(1045-1047)cCt>cTt p.P349L NM_001846 NP_001837 P08572 CO4A2_HUMAN Homo sapiens collagen, type IV, alpha 2 (COL4A2), mRNA. 349 Triple-helical region. angiogenesis|axon guidance|extracellular matrix organization|negative regulation of angiogenesis collagen type IV extracellular matrix structural constituent|protein binding NS(1)|central_nervous_system(3)|endometrium(4)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(4)|liver(2)|lung(48)|ovary(1)|prostate(3)|skin(5)|upper_aerodigestive_tract(3)|urinary_tract(1) 80 all_cancers(4;2.21e-12)|all_epithelial(4;2.63e-07)|all_lung(23;5.81e-06)|Lung NSC(43;0.000274)|Colorectal(4;0.00323)|all_neural(89;0.0565)|Lung SC(71;0.0753)|Medulloblastoma(90;0.0922) Breast(118;0.212) BRCA - Breast invasive adenocarcinoma(86;0.11)|all cancers(43;0.151) CCTGGACTACCTGCCTACTCC 0.483000 5 162 0 0 1 0 0 EGFL8 80864 broad.mit.edu 37 6 32135285 32135285 + Silent SNP C C T rs146401113 byFrequency TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr6:32135285C>T uc003oab.1 + 7 794 c.687C>T c.(685-687)gcC>gcT p.A229A EGFL8_uc003nzy.2_Non-coding_Transcript|EGFL8_uc003oac.1_Silent_p.A229A NM_030652 NP_085155 Q99944 EGFL8_HUMAN Homo sapiens EGF-like-domain, multiple 8 (EGFL8), transcript variant 1, mRNA. 229 extracellular region|integral to membrane calcium ion binding cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(1)|lung(4)|urinary_tract(1) 10 TCTAGTGGGCCGGTCAGGCTG 0.677000 26 48 0 0 1 0 0 GNG5 2787 broad.mit.edu 37 1 84967626 84967626 + Nonsense_Mutation SNP G G A TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr1:84967626G>A uc001djw.4 - 2 463 c.109C>T c.(109-111)Cag>Tag p.Q37* NM_005274 NP_005265 P63218 GBG5_HUMAN Homo sapiens guanine nucleotide binding protein (G protein), gamma 5 (GNG5), mRNA. 37 G-protein coupled receptor protein signaling pathway|cellular response to glucagon stimulus|energy reserve metabolic process|synaptic transmission heterotrimeric G-protein complex GTPase activity|signal transducer activity p.K36N(1) lung(1)|skin(1) 2 all cancers(265;0.00634)|Epithelial(280;0.0175)|OV - Ovarian serous cystadenocarcinoma(397;0.159) AGACAGAACTGTTTCAAGTCT 0.438000 14 34 0 0 1 0 0 INTS1 26173 broad.mit.edu 37 7 1516466 1516466 + Missense_Mutation SNP C C G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr7:1516466C>G uc003skn.2 - 35 5128 c.5027G>C c.(5026-5028)tGc>tCc p.C1676S NM_001080453 NP_001073922 Q8N201 INT1_HUMAN Homo sapiens integrator complex subunit 1 (INTS1), mRNA. 1676 snRNA processing integral to membrane|integrator complex|nuclear membrane autonomic_ganglia(1)|cervix(1)|endometrium(14)|kidney(3)|large_intestine(7)|lung(24)|ovary(1)|prostate(4)|stomach(2)|upper_aerodigestive_tract(3)|urinary_tract(2) 62 Ovarian(82;0.0253) UCEC - Uterine corpus endometrioid carcinoma (27;0.0181)|OV - Ovarian serous cystadenocarcinoma(56;6.99e-15) GACTCGGATGCACTGGTGCAG 0.652000 13 27 0 0 1 0 0 HSPE1-MOB4 100529241 broad.mit.edu 37 2 198413081 198413081 + Missense_Mutation SNP A A G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr2:198413081A>G uc021vum.1 + 6 924 c.484A>G c.(484-486)Aga>Gga p.R162G HSPE1-MOB4_uc002uum.4_Missense_Mutation_p.R94G|HSPE1-MOB4_uc002uun.4_Missense_Mutation_p.R126G|HSPE1-MOB4_uc010fsn.3_Missense_Mutation_p.R105G|HSPE1-MOB4_uc010fso.3_Missense_Mutation_p.R27G|HSPE1-MOB4_uc010zgz.2_Missense_Mutation_p.R27G|HSPE1-MOB4_uc021vun.1_Missense_Mutation_p.R94G NM_001202485 NP_001189414 Homo sapiens HSPE1-MOB4 readthrough (HSPE1-MOB4), mRNA. AGACTATACTAGACACACACT 0.323000 10 57 0 0 1 0 0 TBL2 26608 broad.mit.edu 37 7 72992835 72992835 + Missense_Mutation SNP C C A TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr7:72992835C>A uc003tyh.3 - 0 179 c.45G>T c.(43-45)ttG>ttT p.L15F TBL2_uc011kex.2_5'Flank|TBL2_uc010lbg.3_5'UTR|TBL2_uc003tyi.3_5'UTR|TBL2_uc011key.2_5'UTR NM_012453 NP_036585 Q9Y4P3 TBL2_HUMAN Homo sapiens transducin (beta)-like 2 (TBL2), mRNA. 15 p.V14L(1) endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(3)|lung(7)|prostate(1)|skin(3)|upper_aerodigestive_tract(2) 19 Lung NSC(55;0.0659)|all_lung(88;0.152) GCAGCCCAAGCAACACCGACA 0.711000 7 14 0 0 1 0 0 YLPM1 56252 broad.mit.edu 37 14 75230940 75230940 + Missense_Mutation SNP C C T TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr14:75230940C>T uc001xqj.4 + 0 872 c.748C>T c.(748-750)Ccg>Tcg p.P250S NM_019589 NP_062535 P49750 YLPM1_HUMAN Homo sapiens YLP motif containing 1 (YLPM1), mRNA. 90 regulation of transcription, DNA-dependent|transcription, DNA-dependent nuclear speck breast(4)|cervix(1)|endometrium(7)|haematopoietic_and_lymphoid_tissue(2)|kidney(5)|large_intestine(12)|lung(24)|ovary(3)|pancreas(1)|prostate(1)|skin(1)|urinary_tract(1) 62 KIRC - Kidney renal clear cell carcinoma(43;0.238) BRCA - Breast invasive adenocarcinoma(234;0.00162) TCCACCACCACCGTCCGCCCC 0.567000 10 39 0 0 1 0 0 OR52R1 119695 broad.mit.edu 37 11 4825377 4825377 + Silent SNP G G A TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr11:4825377G>A uc021qcs.1 - 0 234 c.234C>T c.(232-234)tcC>tcT p.S78S NM_001005177 NP_001005177 Q8NGF1 O52R1_HUMAN Homo sapiens olfactory receptor, family 52, subfamily R, member 1 (OR52R1), mRNA. 78 sensory perception of smell integral to membrane|plasma membrane olfactory receptor activity breast(1)|central_nervous_system(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(7)|lung(14)|prostate(1)|skin(3) 29 Medulloblastoma(188;0.0025)|Breast(177;0.0184)|all_neural(188;0.0227) Epithelial(150;4.77e-12)|BRCA - Breast invasive adenocarcinoma(625;0.00435)|LUSC - Lung squamous cell carcinoma(625;0.19) GTTGAGTGGAGGAGGAGAGGA 0.488000 3 56 0 0 1 0 0 EPPK1 83481 broad.mit.edu 37 8 144941609 144941609 + Missense_Mutation SNP C C T TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr8:144941609C>T uc003zaa.1 - 0 5826 c.5813G>A c.(5812-5814)gGg>gAg p.G1938E NM_031308 NP_112598 P58107 EPIPL_HUMAN Homo sapiens epiplakin 1 (EPPK1), mRNA. 1938 cytoplasm|cytoskeleton protein binding|structural molecule activity p.G1938W(1) NS(1)|autonomic_ganglia(1)|breast(1)|central_nervous_system(5)|cervix(1)|endometrium(8)|kidney(4)|large_intestine(2)|lung(30)|ovary(2)|pancreas(1)|prostate(10)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1) 71 all_cancers(97;1.42e-10)|all_epithelial(106;1.99e-09)|Lung NSC(106;0.000126)|all_lung(105;0.000354)|Ovarian(258;0.0173)|Acute lymphoblastic leukemia(118;0.155) OV - Ovarian serous cystadenocarcinoma(54;2.46e-41)|Epithelial(56;2.88e-40)|all cancers(56;1.82e-35)|Colorectal(110;0.055)|BRCA - Breast invasive adenocarcinoma(115;0.105) CAGGAGGAACCCGGTGGCGGC 0.652000 4 52 0 0 1 0 0 ZNF260 339324 broad.mit.edu 37 19 37005674 37005674 + Missense_Mutation SNP T T G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr19:37005674T>G uc002oee.2 - 3 1389 c.467A>C c.(466-468)aAa>aCa p.K156T ZNF260_uc010eey.2_Missense_Mutation_p.K156T|ZNF260_uc002oef.2_Missense_Mutation_p.K156T|ZNF260_uc002oed.2_Missense_Mutation_p.K156T|ZNF260_uc021uti.1_Missense_Mutation_p.K156T NM_001012756 NP_001159510 Q3ZCT1 ZN260_HUMAN Homo sapiens zinc finger protein 260 (ZNF260), transcript variant 1, mRNA. 156 multicellular organismal development|regulation of transcription, DNA-dependent|transcription, DNA-dependent nucleus DNA binding|zinc ion binding endometrium(2)|haematopoietic_and_lymphoid_tissue(1)|kidney(1)|large_intestine(3)|lung(8) 15 Esophageal squamous(110;0.162) AGTATGAATTTTCTCATGCTC 0.398000 38 87 0 0 1 0 0 PMS1 5378 broad.mit.edu 37 2 190732589 190732589 + Missense_Mutation SNP A A G TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr2:190732589A>G uc002urh.4 + 10 2936 c.2407A>G c.(2407-2409)Agt>Ggt p.S803G PMS1_uc002urk.4_Missense_Mutation_p.S764G|PMS1_uc002uri.4_Missense_Mutation_p.S641G|PMS1_uc010zgc.2_Missense_Mutation_p.S627G|PMS1_uc010zgd.2_Missense_Mutation_p.S627G|PMS1_uc002urj.3_Non-coding_Transcript|PMS1_uc010fry.1_Intron|PMS1_uc010frz.3_Intron|PMS1_uc002url.3_Missense_Mutation_p.S426G|PMS1_uc002urm.3_Non-coding_Transcript NM_000534 NP_000525 P54277 PMS1_HUMAN Homo sapiens PMS1 postmeiotic segregation increased 1 (S. cerevisiae) (PMS1), transcript variant 1, mRNA. 803 mismatch repair|reciprocal meiotic recombination MutLalpha complex ATP binding|ATPase activity|mismatched DNA binding breast(3)|central_nervous_system(1)|endometrium(2)|haematopoietic_and_lymphoid_tissue(2)|kidney(3)|large_intestine(5)|lung(16)|ovary(2)|upper_aerodigestive_tract(1)|urinary_tract(1) 36 OV - Ovarian serous cystadenocarcinoma(117;0.0013)|Epithelial(96;0.0263)|all cancers(119;0.0751) CCAAAGATACAGTGGATCAAC 0.323000 """Mis, N""" """colorectal, endometrial, ovarian""" Direct reversal of damage;Mismatch excision repair (MMR) 16 30 0 0 1 0 0 LMX1B 4010 broad.mit.edu 37 9 129456049 129456051 + In_Frame_Del DEL CAG CAG - TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr9:129456049_129456051delCAG uc011maa.2 + 5 851_853 c.844_846delCAG c.(844-846)cagdel p.Q285del LMX1B_uc004bqi.3_In_Frame_Del_p.Q285del|LMX1B_uc004bqj.3_In_Frame_Del_p.Q285del NM_001174146 NP_001167617 O60663 LMX1B_HUMAN Homo sapiens LIM homeobox transcription factor 1, beta (LMX1B), transcript variant 3, mRNA. 262 dorsal/ventral pattern formation|in utero embryonic development nucleus protein binding|sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity|zinc ion binding endometrium(1)|large_intestine(3)|lung(9)|ovary(1)|skin(1) 15 GCGGCGGCACCAGCAGCAGCAGG 0.754 Nail-Patella Syndrome 2 4 --- --- --- --- GRIN2D 2906 broad.mit.edu 37 19 48946470 48946471 + Frame_Shift_Ins INS - - C TCGA-EM-A3FP-01A-11D-A21A-08 TCGA-EM-A3FP-10A-01D-A21A-08 Untested Somatic Phase_I WXS none Illumina GAIIx d8b72d3a-66eb-4718-ae6d-32d7141293aa 42693a6c-5651-4c5e-a16c-e2c6a1d12ebf g.chr19:48946470_48946471insC uc002pjc.4 + 12 3375_3376 c.3287_3288insC c.(3286-3288)tgcfs p.C1096fs GRIN2D_uc010elx.3_Frame_Shift_Ins_p.C331fs|GRWD1_uc002pjd.2_5'Flank NM_000836 NP_000827 O15399 NMDE4_HUMAN Homo sapiens glutamate receptor, ionotropic, N-methyl D-aspartate 2D (GRIN2D), mRNA. 1096 cell junction|outer membrane-bounded periplasmic space|postsynaptic membrane extracellular-glutamate-gated ion channel activity|protein binding autonomic_ganglia(1)|breast(6)|endometrium(2)|large_intestine(9)|lung(12)|ovary(5)|pancreas(1)|prostate(1) 37 all_epithelial(76;1.11e-06)|all_lung(116;5.79e-06)|Lung NSC(112;1.18e-05)|all_neural(266;0.0189)|Ovarian(192;0.0261)|Breast(70;0.203) all cancers(93;0.00014)|OV - Ovarian serous cystadenocarcinoma(262;0.000233)|Epithelial(262;0.0112)|GBM - Glioblastoma multiforme(486;0.0161) L-Glutamic Acid(DB00142)|Loperamide(DB00836)|Orphenadrine(DB01173) ccgcccccgtgccgcgccgcgc 0.817 2 4 --- --- --- ---