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 MASP2 10747 broad.mit.edu 37 1 11087589 11087589 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr1:11087589G>A uc001aru.3 - 10 1446 c.1414C>T c.(1414-1416)Ctt>Ttt p.L472F NM_006610 NP_006601 O00187 MASP2_HUMAN Homo sapiens mannan-binding lectin serine peptidase 2 (MASP2), transcript variant 1, mRNA. 472 Peptidase S1. complement activation, classical pathway|complement activation, lectin pathway|proteolysis extracellular region calcium ion binding|calcium-dependent protein binding|serine-type endopeptidase activity biliary_tract(1)|endometrium(2)|large_intestine(6)|lung(5)|ovary(2)|pancreas(1)|prostate(1)|skin(2)|upper_aerodigestive_tract(1)|urinary_tract(2) 23 Ovarian(185;0.249) Lung NSC(185;1.04e-05)|all_lung(284;1.31e-05)|Renal(390;0.000147)|Colorectal(325;0.00205)|Breast(348;0.00262)|Hepatocellular(190;0.00913)|Ovarian(437;0.00965)|Myeloproliferative disorder(586;0.0255) STAD - Stomach adenocarcinoma(5;0.071) UCEC - Uterine corpus endometrioid carcinoma (279;0.0228)|Colorectal(212;3.12e-07)|COAD - Colon adenocarcinoma(227;7.07e-05)|BRCA - Breast invasive adenocarcinoma(304;0.000293)|Kidney(185;0.000722)|KIRC - Kidney renal clear cell carcinoma(229;0.00258)|READ - Rectum adenocarcinoma(331;0.0487)|STAD - Stomach adenocarcinoma(313;0.192) TCATATAAAAGTGCACCTGCT 0.493 RNF2 6045 broad.mit.edu 37 1 185069006 185069006 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr1:185069006G>A uc001grc.1 + 5 1054 c.821G>A c.(820-822)aGc>aAc p.S274N RNF2_uc001grd.1_Missense_Mutation_p.S202N NM_007212 NP_009143 Q99496 RING2_HUMAN Homo sapiens ring finger protein 2 (RNF2), mRNA. 274 histone H2A monoubiquitination|transcription, DNA-dependent MLL1 complex|PcG protein complex|ubiquitin ligase complex RING-like zinc finger domain binding|zinc ion binding p.R273*(1) breast(3)|endometrium(2)|large_intestine(4)|lung(3)|skin(2) 14 Breast(1374;0.000496) Colorectal(1306;6.9e-08)|KIRC - Kidney renal clear cell carcinoma(1967;8.12e-06) GAACTTCGAAGCAAAGGTGAA 0.393 SOX13 9580 broad.mit.edu 37 1 204085764 204085766 + In_Frame_Del DEL AGC AGC - TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr1:204085764_204085766delAGC uc001ham.3 + 4 1143_1145 c.548_550delAGC c.(547-552)aagcag>aag p.Q187del SOX13_uc001hal.3_In_Frame_Del_p.Q187del|SOX13_uc010pqp.2_In_Frame_Del_p.Q187del|SOX13_uc010pqq.2_In_Frame_Del_p.Q54del NM_005686 NP_005677 Q9UN79 SOX13_HUMAN Homo sapiens SRY (sex determining region Y)-box 13 (SOX13), mRNA. 187 Gln-rich. anatomical structure morphogenesis nucleus sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity breast(1)|central_nervous_system(1)|endometrium(2)|large_intestine(3)|lung(2)|ovary(2)|prostate(2) 13 all_cancers(21;0.0754)|Breast(84;0.116)|all_epithelial(62;0.189) KIRC - Kidney renal clear cell carcinoma(13;0.0584)|Kidney(21;0.0934)|BRCA - Breast invasive adenocarcinoma(75;0.109) CTGTTTGAGAAGCAGCAGCAGCA 0.576 REN 5972 broad.mit.edu 37 1 204135375 204135377 + In_Frame_Del DEL AGC AGC - rs142739309 TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr1:204135375_204135377delAGC uc001haq.2 - 0 89_91 c.45_47delGCT c.(43-48)ctgctc>ctc p.15_16LL>L NM_000537 NP_000528 P00797 RENI_HUMAN Homo sapiens renin (REN), mRNA. 15 angiotensin maturation|regulation of MAPKKK cascade extracellular space|membrane aspartic-type endopeptidase activity NS(1)|central_nervous_system(1)|endometrium(1)|kidney(1)|large_intestine(6)|lung(3)|ovary(1)|skin(4)|urinary_tract(1) 19 all_cancers(21;0.00965)|Breast(84;0.116)|all_epithelial(62;0.157) KIRC - Kidney renal clear cell carcinoma(13;0.0584)|Kidney(21;0.0934)|BRCA - Breast invasive adenocarcinoma(75;0.109) Aliskiren(DB01258)|Remikiren(DB00212) GGAGCCCCAGAGCAGCAGCAGCA 0.581 OR2C3 81472 broad.mit.edu 37 1 247695277 247695277 + Silent SNP A A G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr1:247695277A>G uc021pmb.1 - 0 537 c.537T>C c.(535-537)ttT>ttC p.F179F C1orf150_uc009xgw.3_Intron|C1orf150_uc001ida.4_Intron|C1orf150_uc001idb.4_Intron|C1orf150_uc009xgx.3_Intron|OR2C3_uc001idd.3_5'Flank|OR2C3_uc009xgy.3_Silent_p.F179F NM_198074 NP_932340 Q8N628 OR2C3_HUMAN Homo sapiens olfactory receptor, family 2, subfamily C, member 3 (OR2C3), mRNA. 179 sensory perception of smell integral to membrane|plasma membrane olfactory receptor activity breast(1)|endometrium(5)|large_intestine(2)|lung(31)|ovary(1)|prostate(1)|skin(2) 43 all_cancers(71;4.51e-05)|all_epithelial(71;1.3e-05)|Breast(184;0.0149)|Ovarian(71;0.0377)|all_lung(81;0.0662)|Lung NSC(105;0.0724) all_cancers(173;0.0242) OV - Ovarian serous cystadenocarcinoma(106;0.0241) GCATCTCGCAAAAGAAGTGGT 0.557 PTEN 5728 broad.mit.edu 37 10 89692904 89692904 + Nonsense_Mutation SNP C C T rs121913292 TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr10:89692904C>T uc001kfb.3 + 4 1420 c.388C>T c.(388-390)Cga>Tga p.R130* PTEN_uc021pvw.1_Non-coding_Transcript NM_000314 NP_000305 P60484 PTEN_HUMAN Homo sapiens phosphatase and tensin homolog (PTEN), mRNA. 130 Phosphatase tensin-type. R -> G (loss of phosphatase activity towards Ins(1,3,4,5)P4 and PtdIns(3,4,5)P3).|R -> L (in CD and endometrial hyperplasia; loss of phosphatase activity towards Ins(1,3,4,5)P4; retains ability to bind phospholipid membranes).|R -> Q (in CD; loss of phosphatase activity towards Ins(1,3,4,5)P4; retains ability to bind phospholipid membranes). activation of mitotic anaphase-promoting complex activity|apoptosis|canonical Wnt receptor signaling pathway|cell proliferation|central nervous system development|induction of apoptosis|inositol phosphate dephosphorylation|negative regulation of cell migration|negative regulation of cyclin-dependent protein kinase activity involved in G1/S|negative regulation of focal adhesion assembly|negative regulation of G1/S transition of mitotic cell cycle|negative regulation of protein kinase B signaling cascade|negative regulation of protein phosphorylation|nerve growth factor receptor signaling pathway|phosphatidylinositol dephosphorylation|phosphatidylinositol-mediated signaling|positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process|positive regulation of sequence-specific DNA binding transcription factor activity|protein stabilization|regulation of neuron projection development|T cell receptor signaling pathway cytosol|internal side of plasma membrane|PML body anaphase-promoting complex binding|enzyme binding|inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity|lipid binding|magnesium ion binding|PDZ domain binding|phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase activity|phosphatidylinositol-3,4-bisphosphate 3-phosphatase activity|phosphatidylinositol-3-phosphatase activity|protein serine/threonine phosphatase activity|protein tyrosine phosphatase activity|protein tyrosine/serine/threonine phosphatase activity p.R130G(212)|p.R130*(135)|p.R130Q(68)|p.0?(37)|p.R130fs*4(16)|p.R130L(13)|p.K128_R130del(8)|p.R130P(7)|p.G129R(7)|p.?(5)|p.R55fs*1(5)|p.G129*(4)|p.G129V(3)|p.R130R(2)|p.Y27_N212>Y(2)|p.G129E(2)|p.A121_F145del(2)|p.Y27fs*1(2)|p.G129fs*50(2)|p.G129fs*51(2)|p.K128fs*47(1)|p.F56fs*2(1)|p.G129fs*5(1)|p.R130?(1)|p.R130fs*2(1) NS(28)|autonomic_ganglia(2)|biliary_tract(6)|bone(5)|breast(92)|central_nervous_system(676)|cervix(26)|endometrium(1068)|eye(8)|haematopoietic_and_lymphoid_tissue(137)|kidney(24)|large_intestine(98)|liver(20)|lung(91)|meninges(2)|oesophagus(2)|ovary(82)|pancreas(6)|prostate(129)|salivary_gland(5)|skin(127)|soft_tissue(19)|stomach(30)|testis(1)|thyroid(29)|upper_aerodigestive_tract(29)|urinary_tract(12)|vulva(17) 2771 all_cancers(4;3.61e-31)|all_epithelial(4;3.96e-23)|Prostate(4;8.12e-23)|Breast(4;0.000111)|Melanoma(5;0.00146)|all_hematologic(4;0.00227)|Colorectal(252;0.00494)|all_neural(4;0.00513)|Acute lymphoblastic leukemia(4;0.0116)|Glioma(4;0.0274)|all_lung(38;0.132) KIRC - Kidney renal clear cell carcinoma(1;0.214) UCEC - Uterine corpus endometrioid carcinoma (6;0.000228)|all cancers(1;4.16e-84)|GBM - Glioblastoma multiforme(1;7.77e-49)|Epithelial(1;7.67e-41)|OV - Ovarian serous cystadenocarcinoma(1;6.22e-15)|BRCA - Breast invasive adenocarcinoma(1;1.1e-06)|Lung(2;3.18e-06)|Colorectal(12;4.88e-06)|LUSC - Lung squamous cell carcinoma(2;4.97e-06)|COAD - Colon adenocarcinoma(12;1.13e-05)|Kidney(1;0.000288)|KIRC - Kidney renal clear cell carcinoma(1;0.00037)|STAD - Stomach adenocarcinoma(243;0.218) TGGAAAGGGACGAACTGGTGT 0.403 R130G(KMBC2_URINARY_TRACT)|R130G(OV56_OVARY) 31 """D, Mis, N, F, S""" """glioma, prostate, endometrial""" """harmartoma, glioma, prostate, endometrial""" Proteus syndrome;Juvenile Polyposis;Hereditary Mixed Polyposis Syndrome type 1;Cowden syndrome;Bannayan-Riley-Ruvalcaba syndrome HNSCC(9;0.0022)|TCGA GBM(2;<1E-08)|TSP Lung(26;0.18) ANO9 338440 broad.mit.edu 37 11 420528 420528 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr11:420528C>T uc001lpi.2 - 18 1806 c.1721G>A c.(1720-1722)cGc>cAc p.R574H ANO9_uc001lph.2_Missense_Mutation_p.R267H|ANO9_uc010qvv.1_Missense_Mutation_p.R430H NM_001012302 NP_001012302 A1A5B4 ANO9_HUMAN Homo sapiens anoctamin 9 (ANO9), mRNA. 574 chloride channel complex chloride channel activity central_nervous_system(2)|cervix(1)|endometrium(3)|kidney(1)|lung(5)|ovary(1)|prostate(4)|skin(4) 21 GGCGTCCAGGCGGATCTCCAC 0.682 OR4D11 219986 broad.mit.edu 37 11 59271634 59271634 + Nonsense_Mutation SNP G G T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr11:59271634G>T uc001noa.1 + 0 586 c.586G>T c.(586-588)Gag>Tag p.E196* NM_001004706 NP_001004706 Q8NGI4 OR4DB_HUMAN Homo sapiens olfactory receptor, family 4, subfamily D, member 11 (OR4D11), mRNA. 196 sensory perception of smell integral to membrane|plasma membrane olfactory receptor activity p.L195H(1) endometrium(2)|large_intestine(3)|liver(2)|lung(17)|ovary(1)|prostate(1)|skin(1)|stomach(1)|upper_aerodigestive_tract(1) 29 TTTTGCTCTTGAGTTCTTGAT 0.493 CTTN 2017 broad.mit.edu 37 11 70255986 70255986 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr11:70255986G>A uc001opv.4 + 4 417 c.211G>A c.(211-213)Gag>Aag p.E71K CTTN_uc001opu.3_Missense_Mutation_p.E71K|CTTN_uc001opw.4_Missense_Mutation_p.E71K NM_005231 NP_005222 Q14247 SRC8_HUMAN Homo sapiens cortactin (CTTN), transcript variant 1, mRNA. 71 cell cortex|cytoskeleton|lamellipodium|ruffle|soluble fraction protein binding p.K70N(1) breast(2)|cervix(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|large_intestine(3)|lung(14)|ovary(1)|pancreas(1)|prostate(3)|skin(1)|urinary_tract(1) 31 BRCA - Breast invasive adenocarcinoma(2;4.34e-41)|LUSC - Lung squamous cell carcinoma(11;1.51e-13)|STAD - Stomach adenocarcinoma(18;0.0513) Lung(977;0.0234)|LUSC - Lung squamous cell carcinoma(976;0.133) GACCCTTAAGGAGAAGGAACT 0.468 PRB3 5544 broad.mit.edu 37 12 11420518 11420518 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr12:11420518G>A uc001qzs.3 - 2 703 c.665C>T c.(664-666)cCg>cTg p.P222L PRB4_uc001qzf.1_Intron NM_006249 NP_006240 Q04118 PRB3_HUMAN Homo sapiens proline-rich protein BstNI subfamily 3 (PRB3), mRNA. 222 10 X 21 AA tandem repeats of [RH]-P-G-K- P-[EQ]-G-[PQS]-P-[PS]-Q-[GE]-G-N-[QK]- [SP]-[QR]-[GR]-P-P-P.|Pro-rich. extracellular region Gram-negative bacterial cell surface binding p.R221S(2) breast(2)|endometrium(1)|kidney(2)|large_intestine(1)|lung(13)|ovary(1)|skin(5) 25 OV - Ovarian serous cystadenocarcinoma(49;0.201) TGGCTTTCCCGGACGAGGTGG 0.617 PRB3 5544 broad.mit.edu 37 12 11420581 11420581 + Missense_Mutation SNP G G A rs71057716 TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr12:11420581G>A uc001qzs.3 - 2 640 c.602C>T c.(601-603)cCg>cTg p.P201L PRB4_uc001qzf.1_Intron NM_006249 NP_006240 Q04118 PRB3_HUMAN Homo sapiens proline-rich protein BstNI subfamily 3 (PRB3), mRNA. 201 10 X 21 AA tandem repeats of [RH]-P-G-K- P-[EQ]-G-[PQS]-P-[PS]-Q-[GE]-G-N-[QK]- [SP]-[QR]-[GR]-P-P-P.|Pro-rich. Missing (in allele S). extracellular region Gram-negative bacterial cell surface binding p.R200C(1) breast(2)|endometrium(1)|kidney(2)|large_intestine(1)|lung(13)|ovary(1)|skin(5) 25 OV - Ovarian serous cystadenocarcinoma(49;0.201) TGGCTTTCCCGGACGAGGTGG 0.632 MYF6 4618 broad.mit.edu 37 12 81101720 81101720 + Silent SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr12:81101720C>T uc001szf.2 + 0 313 c.222C>T c.(220-222)ccC>ccT p.P74P NM_002469 NP_002460 P23409 MYF6_HUMAN Homo sapiens myogenic factor 6 (herculin) (MYF6), mRNA. 74 muscle cell fate commitment|positive regulation of muscle cell differentiation|positive regulation of transcription from RNA polymerase II promoter|skeletal muscle tissue development nucleoplasm DNA binding|protein heterodimerization activity|sequence-specific DNA binding transcription factor activity central_nervous_system(1)|cervix(1)|endometrium(3)|kidney(3)|large_intestine(5)|lung(12)|skin(1) 26 CACACTGCCCCGGCCAGTGTC 0.652 UBC 7316 broad.mit.edu 37 12 125397269 125397269 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr12:125397269G>A uc001ugs.4 - 1 1507 c.1049C>T c.(1048-1050)gCc>gTc p.A350V UBC_uc001ugr.3_Intron|UBC_uc001ugt.3_Missense_Mutation_p.A350V|UBC_uc001ugu.1_Missense_Mutation_p.A350V|UBC_uc001ugv.3_Intron|UBC_uc021rge.1_Missense_Mutation_p.A350V|UBC_uc001ugw.3_Missense_Mutation_p.A198V NM_021009 NP_066289 P0CG48 UBC_HUMAN Homo sapiens ubiquitin C (UBC), mRNA. 350 Ubiquitin-like 5. activation of MAPK activity|anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process|anti-apoptosis|apoptosis|cellular membrane organization|DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest|DNA repair|endosome transport|epidermal growth factor receptor signaling pathway|G1/S transition of mitotic cell cycle|I-kappaB kinase/NF-kappaB cascade|induction of apoptosis by extracellular signals|innate immune response|JNK cascade|M/G1 transition of mitotic cell cycle|mRNA metabolic process|MyD88-dependent toll-like receptor signaling pathway|MyD88-independent toll-like receptor signaling pathway|negative regulation of epidermal growth factor receptor signaling pathway|negative regulation of type I interferon production|negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle|nerve growth factor receptor signaling pathway|positive regulation of I-kappaB kinase/NF-kappaB cascade|positive regulation of NF-kappaB transcription factor activity|positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle|S phase of mitotic cell cycle|stress-activated MAPK cascade|T cell receptor signaling pathway|Toll signaling pathway|toll-like receptor 1 signaling pathway|toll-like receptor 2 signaling pathway|toll-like receptor 3 signaling pathway|toll-like receptor 4 signaling pathway|viral reproduction cytosol|endocytic vesicle membrane|endosome membrane|nucleoplasm|plasma membrane protein binding breast(3)|endometrium(4)|kidney(4)|large_intestine(2)|lung(13)|ovary(3)|prostate(4)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(1) 36 all_neural(191;0.101)|Medulloblastoma(191;0.163) OV - Ovarian serous cystadenocarcinoma(86;6.17e-05)|Epithelial(86;0.000207)|all cancers(50;0.00308) CTGTTTTCCGGCAAAGATCAA 0.522 CCNA1 8900 broad.mit.edu 37 13 37011790 37011790 + Missense_Mutation SNP T T A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr13:37011790T>A uc001uvr.4 + 2 672 c.322T>A c.(322-324)Tct>Act p.S108T CCNA1_uc010teo.2_Missense_Mutation_p.S64T|CCNA1_uc010abq.3_Missense_Mutation_p.S64T|CCNA1_uc010abp.3_Missense_Mutation_p.S64T|CCNA1_uc001uvs.4_Missense_Mutation_p.S107T|CCNA1_uc010abr.3_Non-coding_Transcript NM_003914 NP_001104517 P78396 CCNA1_HUMAN Homo sapiens cyclin A1 (CCNA1), transcript variant 1, mRNA. 108 cell division|G2/M transition of mitotic cell cycle|male meiosis I|mitosis|regulation of cyclin-dependent protein kinase activity|regulation of transcription involved in G1/S phase of mitotic cell cycle|spermatogenesis cytosol|microtubule cytoskeleton|nucleoplasm protein kinase binding p.Y107Y(1) breast(1)|endometrium(3)|kidney(4)|large_intestine(8)|lung(10)|ovary(3)|prostate(1)|skin(2)|stomach(2)|urinary_tract(1) 35 Breast(139;0.014)|Lung SC(185;0.0548)|Prostate(109;0.174) KIRC - Kidney renal clear cell carcinoma(5;0.119)|Kidney(79;0.169) all cancers(112;1.91e-07)|Epithelial(112;1.22e-05)|OV - Ovarian serous cystadenocarcinoma(117;0.00623)|BRCA - Breast invasive adenocarcinoma(63;0.0119)|GBM - Glioblastoma multiforme(144;0.0242) CAGGTGTTATTCTGGATCAGA 0.468 C15orf2 23742 broad.mit.edu 37 15 24921520 24921520 + Missense_Mutation SNP T T C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr15:24921520T>C uc001ywo.3 + 0 980 c.506T>C c.(505-507)aTc>aCc p.I169T NM_018958 NP_061831 Q9NZP6 CO002_HUMAN Homo sapiens chromosome 15 open reading frame 2 (C15orf2), mRNA. 169 cell differentiation|multicellular organismal development|spermatogenesis NS(2)|autonomic_ganglia(1)|breast(1)|central_nervous_system(2)|cervix(1)|endometrium(13)|kidney(1)|large_intestine(28)|lung(77)|ovary(5)|pancreas(1)|skin(8) 140 all_cancers(20;2.14e-21)|all_epithelial(15;4.77e-19)|Lung NSC(15;1.43e-14)|all_lung(15;9.57e-14)|Breast(32;0.00086) all cancers(64;3.19e-24)|Epithelial(43;2.67e-17)|GBM - Glioblastoma multiforme(186;7.36e-07)|BRCA - Breast invasive adenocarcinoma(123;0.000273)|Lung(196;0.229) CCGGTGCAGATCGAAGGGGAG 0.612 GOLGA6L10 647042 broad.mit.edu 37 15 83014106 83014106 + Silent SNP T T C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr15:83014106T>C uc021ssz.1 - 5 577 c.441A>G c.(439-441)gtA>gtG p.V147V LOC440295_uc002bhl.2_Intron|GOLGA6L9_uc021ssr.1_Intron|LOC440295_uc002bhm.2_Intron|GOLGA6L10_uc021sta.1_Non-coding_Transcript A6NI86 GG6LA_HUMAN Homo sapiens golgin A6 family-like 10 (GOLGA6L10), mRNA. 159 p.V159V(12) endometrium(1)|kidney(4) 5 GTAGCTGCTCTACCTTAGATG 0.498 MYO15A 51168 broad.mit.edu 37 17 18024801 18024801 + Frame_Shift_Del DEL G G - TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr17:18024801delG uc021trm.1 + 0 2906 c.2687delG c.(2686-2688)aggfs p.R896fs MYO15A_uc021trl.1_Frame_Shift_Del_p.R896fs NM_016239 NP_057323 Q9UKN7 MYO15_HUMAN Homo sapiens myosin XVA (MYO15A), mRNA. 896 Myosin head-like. sensory perception of sound cytoplasm|myosin complex|stereocilium actin binding|ATP binding|calmodulin binding|motor activity breast(5)|central_nervous_system(2)|endometrium(17)|kidney(3)|large_intestine(16)|lung(27)|ovary(3)|pancreas(1)|prostate(6)|skin(13)|stomach(1)|upper_aerodigestive_tract(3)|urinary_tract(2) 99 all_neural(463;0.228) CGACCGCCCAGGGCCGGGGCC 0.741 DSG4 147409 broad.mit.edu 37 18 28992962 28992962 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr18:28992962C>T uc002kwr.2 + 14 2719 c.2584C>T c.(2584-2586)Ctt>Ttt p.L862F DSG4_uc002kwq.2_Missense_Mutation_p.L843F NM_001134453 NP_001127925 Q86SJ6 DSG4_HUMAN Homo sapiens desmoglein 4 (DSG4), transcript variant 1, mRNA. 843 homophilic cell adhesion desmosome|integral to membrane calcium ion binding NS(1)|breast(1)|central_nervous_system(6)|cervix(1)|endometrium(1)|haematopoietic_and_lymphoid_tissue(3)|kidney(2)|large_intestine(11)|liver(2)|lung(35)|ovary(4)|skin(1)|stomach(1)|urinary_tract(1) 70 OV - Ovarian serous cystadenocarcinoma(10;0.00504) ATTTAGGACTCTTGCTGAGAT 0.438 LMAN1 3998 broad.mit.edu 37 18 57014768 57014768 + Silent SNP A A G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr18:57014768A>G uc002lhz.3 - 6 831 c.799T>C c.(799-801)Ttg>Ctg p.L267L NM_005570 NP_005561 P49257 LMAN1_HUMAN Homo sapiens lectin, mannose-binding, 1 (LMAN1), mRNA. 267 L-type lectin-like. blood coagulation|ER to Golgi vesicle-mediated transport|post-translational protein modification|protein folding|protein N-linked glycosylation via asparagine|protein transport endoplasmic reticulum membrane|ER to Golgi transport vesicle membrane|ER-Golgi intermediate compartment membrane|Golgi membrane|integral to membrane mannose binding|metal ion binding|unfolded protein binding breast(2)|endometrium(1)|kidney(2)|large_intestine(3)|lung(5)|ovary(1)|prostate(1)|skin(1) 16 Colorectal(73;0.0946) Antihemophilic Factor(DB00025) GGTTCAGTCAACTGGAAAGTC 0.313 CEACAM20 125931 broad.mit.edu 37 19 45016954 45016954 + Silent SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr19:45016954C>T uc010ejn.1 - 8 1501 c.1485G>A c.(1483-1485)aaG>aaA p.K495K CEACAM20_uc010ejo.1_Silent_p.K495K|CEACAM20_uc010ejp.1_Silent_p.K402K|CEACAM20_uc010ejq.1_Silent_p.K402K NM_001102597 NP_001096067 Q6UY09 CEA20_HUMAN Homo sapiens carcinoembryonic antigen-related cell adhesion molecule 20 (CEACAM20), transcript variant 5L, mRNA. 495 integral to membrane central_nervous_system(1)|endometrium(2)|kidney(1)|large_intestine(2)|lung(8)|prostate(1) 15 Prostate(69;0.0352) GGTGCTCCTCCTTCGGGATGG 0.587 OREG0025538 type=REGULATORY REGION|TFbs=CTCF|Dataset=CTCF ChIP-chip sites (Ren lab)|EvidenceSubtype=ChIP-on-chip (ChIP-chip) A1BG 1 broad.mit.edu 37 19 58858802 58858802 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr19:58858802C>T uc002qsd.4 - 6 1459 c.1397G>A c.(1396-1398)gGc>gAc p.G466D A1BG-AS1_uc002qse.3_5'Flank NM_130786 NP_570602 P04217 A1BG_HUMAN Homo sapiens alpha-1-B glycoprotein (A1BG), mRNA. 466 Ig-like V-type 5. extracellular region NS(1)|cervix(1)|endometrium(1)|kidney(2)|large_intestine(1)|lung(7)|prostate(2) 15 all_cancers(17;3.04e-16)|all_epithelial(17;7.77e-12)|Lung NSC(17;3.25e-05)|Colorectal(82;5.46e-05)|all_lung(17;0.000129)|all_neural(62;0.0182)|Ovarian(87;0.0443)|Breast(46;0.0889)|Renal(17;0.157) UCEC - Uterine corpus endometrioid carcinoma (67;0.168)|GBM - Glioblastoma multiforme(193;0.0269) CCTGTAGTTGCCGGCGTGCTG 0.692 PIGF 5281 broad.mit.edu 37 2 46808672 46808672 + Missense_Mutation SNP A A G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr2:46808672A>G uc002rvd.3 - 5 769 c.605T>C c.(604-606)aTt>aCt p.I202T RHOQ_uc002rva.3_3'UTR|BC048424_uc002rvb.3_5'Flank|PIGF_uc002rvc.3_3'UTR NM_002643 NP_002634 Q07326 PIGF_HUMAN Homo sapiens phosphatidylinositol glycan anchor biosynthesis, class F (PIGF), transcript variant 1, mRNA. 202 C-terminal protein lipidation|preassembly of GPI anchor in ER membrane endoplasmic reticulum membrane|integral to membrane ethanolaminephosphotransferase activity breast(1)|endometrium(1)|lung(1)|stomach(1) 4 all_hematologic(82;0.151)|Acute lymphoblastic leukemia(82;0.175) LUSC - Lung squamous cell carcinoma(58;0.114) GAGTGGTGAAATAACAAGGCC 0.418 LBX2 85474 broad.mit.edu 37 2 74729804 74729804 + Silent SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr2:74729804G>A uc002slw.3 - 0 640 c.183C>T c.(181-183)tgC>tgT p.C61C LOC151534_uc002slx.2_Non-coding_Transcript NM_001009812 NP_001009812 Q6XYB7 LBX2_HUMAN Homo sapiens ladybird homeobox 2 (LBX2), mRNA. 64 nucleus sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity central_nervous_system(1)|kidney(1)|large_intestine(1)|lung(1) 4 TTTGGGGGCGGCAGGCCTGTG 0.602 FAM176A 84141 broad.mit.edu 37 2 75720689 75720689 + Silent SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr2:75720689G>A uc002sni.2 - 3 610 c.132C>T c.(130-132)atC>atT p.I44I FAM176A_uc002snj.1_Silent_p.I31I|FAM176A_uc002snk.1_Silent_p.I44I NM_001135032 NP_115557 Q9H8M9 F176A_HUMAN Homo sapiens family with sequence similarity 176, member A (FAM176A), transcript variant 1, mRNA. 44 Necessary for the localization and biological activity. apoptosis|autophagy endoplasmic reticulum membrane|integral to membrane|lysosomal membrane|plasma membrane endometrium(1)|large_intestine(4)|lung(1)|skin(2) 8 GCACCAGCCCGATGCACACGC 0.537 DNAH7 56171 broad.mit.edu 37 2 196689149 196689149 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr2:196689149C>T uc002utj.4 - 48 9222 c.9121G>A c.(9121-9123)Gaa>Aaa p.E3041K NM_018897 NP_061720 Q8WXX0 DYH7_HUMAN Homo sapiens dynein, axonemal, heavy chain 7 (DNAH7), mRNA. 3041 AAA 5 (By similarity). ciliary or flagellar motility|microtubule-based movement axonemal dynein complex|cilium axoneme|cytoplasm|microtubule ATP binding|microtubule motor activity NS(4)|breast(2)|endometrium(12)|haematopoietic_and_lymphoid_tissue(1)|kidney(15)|large_intestine(28)|liver(3)|lung(100)|ovary(4)|prostate(5)|skin(26)|upper_aerodigestive_tract(2)|urinary_tract(3) 205 TCTAGTTCTTCGCCAACATTT 0.348 ABI2 10152 broad.mit.edu 37 2 204260428 204260428 + Nonsense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr2:204260428C>T uc002vaa.3 + 6 1010 c.775C>T c.(775-777)Cga>Tga p.R259* ABI2_uc010zig.1_Non-coding_Transcript|ABI2_uc010zij.2_Nonsense_Mutation_p.R197*|ABI2_uc002uzz.3_Nonsense_Mutation_p.R253*|ABI2_uc010zih.2_Intron|ABI2_uc010zii.2_Nonsense_Mutation_p.R253*|ABI2_uc002vab.3_Nonsense_Mutation_p.R208*|ABI2_uc010zik.2_Nonsense_Mutation_p.R45*|ABI2_uc010zil.2_Nonsense_Mutation_p.R94*|ABI2_uc010zim.2_Nonsense_Mutation_p.R45*|ABI2_uc002vac.3_Nonsense_Mutation_p.R45*|ABI2_uc010zin.2_Intron NM_005759 NP_005750 Q9NYB9 ABI2_HUMAN Homo sapiens abl-interactor 2 (ABI2), mRNA. 259 Pro-rich. actin polymerization or depolymerization|cell migration|peptidyl-tyrosine phosphorylation cytoskeleton|cytosol|filopodium|lamellipodium cytoskeletal adaptor activity|DNA binding|kinase binding|proline-rich region binding|SH3 domain binding|ubiquitin protein ligase binding breast(1)|kidney(3)|large_intestine(1)|liver(2)|lung(4)|prostate(2)|skin(1)|urinary_tract(1) 15 GAGCAGCAGTCGAGAGAACAG 0.478 KIF16B 55614 broad.mit.edu 37 20 16337022 16337022 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr20:16337022C>T uc002wpg.2 - 22 3733 c.3574G>A c.(3574-3576)Gtc>Atc p.V1192I KIF16B_uc002wpe.1_Missense_Mutation_p.V574I|KIF16B_uc002wpf.1_Intron|KIF16B_uc010gch.2_Missense_Mutation_p.V1141I NM_024704 NP_078980 Q96L93 KI16B_HUMAN Homo sapiens kinesin family member 16B (KIF16B), transcript variant 2, mRNA. 1192 PX. cell communication|early endosome to late endosome transport|endoderm development|epidermal growth factor receptor signaling pathway|fibroblast growth factor receptor signaling pathway|formation of primary germ layer|Golgi to endosome transport|microtubule-based movement|receptor catabolic process|regulation of receptor recycling early endosome membrane|microtubule ATP binding|phosphatidylinositol-3,4,5-trisphosphate binding|phosphatidylinositol-3,4-bisphosphate binding|phosphatidylinositol-3,5-bisphosphate binding|phosphatidylinositol-3-phosphate binding|plus-end-directed microtubule motor activity NS(2)|breast(1)|central_nervous_system(1)|cervix(1)|endometrium(3)|kidney(6)|large_intestine(15)|lung(24)|ovary(1)|prostate(15)|skin(3)|upper_aerodigestive_tract(2) 74 CCGCAGAGGACGTAGCGTGGG 0.498 PCK1 5105 broad.mit.edu 37 20 56137841 56137841 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr20:56137841G>A uc002xyn.4 + 3 659 c.496G>A c.(496-498)Gtg>Atg p.V166M PCK1_uc010zzm.2_Intron NM_002591 NP_002582 P35558 PCKGC_HUMAN Homo sapiens phosphoenolpyruvate carboxykinase 1 (soluble) (PCK1), mRNA. 166 gluconeogenesis|glucose homeostasis|glycerol biosynthetic process from pyruvate|response to insulin stimulus cytosol|nucleus carboxylic acid binding|GTP binding|magnesium ion binding|manganese ion binding|phosphoenolpyruvate carboxykinase (GTP) activity endometrium(2)|kidney(1)|large_intestine(4)|liver(2)|lung(19)|pancreas(1)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(3) 34 Lung NSC(12;0.000764)|all_lung(29;0.00264)|Melanoma(10;0.242) BRCA - Breast invasive adenocarcinoma(13;9.88e-12)|Epithelial(14;3.41e-08)|all cancers(14;2.13e-07) TTCACCCTACGTGGTGGCCAG 0.617 NRIP1 8204 broad.mit.edu 37 21 16340303 16340303 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr21:16340303G>A uc021whl.1 - 0 211 c.211C>T c.(211-213)Cat>Tat p.H71Y NRIP1_uc002yjx.2_Missense_Mutation_p.H71Y NM_003489 NP_003480 P48552 NRIP1_HUMAN Homo sapiens nuclear receptor interacting protein 1 (NRIP1), mRNA. 71 androgen receptor signaling pathway|negative regulation of transcription from RNA polymerase II promoter|positive regulation of transcription from RNA polymerase II promoter|transcription, DNA-dependent androgen receptor binding|estrogen receptor binding|glucocorticoid receptor binding|transcription coactivator activity|transcription corepressor activity cervix(3)|haematopoietic_and_lymphoid_tissue(2)|kidney(5)|large_intestine(6)|lung(13)|prostate(4)|skin(1)|upper_aerodigestive_tract(1)|urinary_tract(4) 39 Epithelial(23;1.19e-05)|all cancers(11;4.64e-05)|COAD - Colon adenocarcinoma(22;0.000232)|Colorectal(24;0.0006)|OV - Ovarian serous cystadenocarcinoma(11;0.00418)|Lung(58;0.199)|LUSC - Lung squamous cell carcinoma(23;0.24) TGATATGTATGTGTATTGAGA 0.458 TIAM1 7074 broad.mit.edu 37 21 32639088 32639088 + Silent SNP G G C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr21:32639088G>C uc002yow.1 - 4 673 c.201C>G c.(199-201)tcC>tcG p.S67S TIAM1_uc011adk.1_Silent_p.S67S|TIAM1_uc011adl.1_Silent_p.S67S|TIAM1_uc002yox.1_Intron NM_003253 NP_003244 Q13009 TIAM1_HUMAN Homo sapiens T-cell lymphoma invasion and metastasis 1 (TIAM1), mRNA. 67 apoptosis|induction of apoptosis by extracellular signals|nerve growth factor receptor signaling pathway|regulation of Rho protein signal transduction|small GTPase mediated signal transduction cell-cell junction|cytosol receptor signaling protein activity|Rho guanyl-nucleotide exchange factor activity autonomic_ganglia(3)|breast(7)|central_nervous_system(2)|endometrium(13)|kidney(4)|large_intestine(33)|lung(44)|ovary(2)|prostate(3)|skin(2)|urinary_tract(2) 115 TTTCAGCCAGGGACTGGGGGA 0.617 CBR1 873 broad.mit.edu 37 21 37445093 37445093 + Missense_Mutation SNP G G T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr21:37445093G>T uc002yvb.1 + 2 876 c.747G>T c.(745-747)gaG>gaT p.E249D LOC100133286_uc011aea.1_Intron|SETD4_uc002yva.3_Intron|CBR1_uc010gmy.1_3'UTR NM_001757 NP_001748 P16152 CBR1_HUMAN Homo sapiens carbonyl reductase 1 (CBR1), mRNA. 249 drug metabolic process|vitamin K metabolic process cytoplasm 15-hydroxyprostaglandin dehydrogenase (NADP+) activity|carbonyl reductase (NADPH) activity|prostaglandin-E2 9-reductase activity|protein binding endometrium(2)|kidney(3) 5 Acetohexamide(DB00414)|Lubiprostone(DB01046) AAGGTGCAGAGACCCCTGTGT 0.572 TSPEAR 54084 broad.mit.edu 37 21 45953585 45953585 + Silent SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr21:45953585G>A uc002zfe.1 - 2 591 c.525C>T c.(523-525)tgC>tgT p.C175C TSPEAR_uc010gpv.1_Silent_p.C107C NM_144991 NP_659428 Q8WU66 TSEAR_HUMAN Homo sapiens thrombospondin-type laminin G domain and EAR repeats (TSPEAR), mRNA. 175 TSP N-terminal. cell adhesion extracellular region structural molecule activity breast(1)|central_nervous_system(6)|cervix(1)|endometrium(2)|kidney(2)|large_intestine(7)|lung(7)|ovary(1)|pancreas(1)|skin(6)|soft_tissue(1)|upper_aerodigestive_tract(2) 37 CCGGGAGGCCGCAGTCCGTGG 0.682 RAF1 5894 broad.mit.edu 37 3 12632402 12632402 + Missense_Mutation SNP T T C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr3:12632402T>C uc003bxf.4 - 11 1680 c.1265A>G c.(1264-1266)cAg>cGg p.Q422R RAF1_uc011aut.2_Missense_Mutation_p.Q207R|RAF1_uc011auu.2_Missense_Mutation_p.Q340R NM_002880 NP_002871 P04049 RAF1_HUMAN Homo sapiens v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1), mRNA. 422 Protein kinase. activation of MAPKK activity|apoptosis|axon guidance|cell proliferation|epidermal growth factor receptor signaling pathway|insulin receptor signaling pathway|negative regulation of apoptosis|negative regulation of cell proliferation|negative regulation of protein complex assembly|nerve growth factor receptor signaling pathway|platelet activation|positive regulation of peptidyl-serine phosphorylation|Ras protein signal transduction|synaptic transmission cytosol|mitochondrial outer membrane|plasma membrane ATP binding|metal ion binding|protein binding|protein serine/threonine kinase activity|receptor signaling protein activity ESRP1/RAF1(4)|RAF1/DAZL(2)|SRGAP3/RAF1(6) biliary_tract(1)|endometrium(4)|kidney(3)|large_intestine(9)|liver(1)|lung(7)|ovary(1)|pancreas(1)|prostate(2)|stomach(2)|upper_aerodigestive_tract(1) 32 Sorafenib(DB00398) CTCGCACCACTGGGTCACAAT 0.542 T SRGAP3 pilocytic astrocytoma Noonan syndrome SCN5A 6331 broad.mit.edu 37 3 38591931 38591931 + Missense_Mutation SNP C C G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr3:38591931C>G uc021wvo.1 - 26 5984 c.5932G>C c.(5932-5934)Gac>Cac p.D1978H SCN5A_uc021wvk.1_Missense_Mutation_p.D1945H|SCN5A_uc021wvl.1_Missense_Mutation_p.D1924H|SCN5A_uc021wvm.1_Missense_Mutation_p.D1960H|SCN5A_uc021wvn.1_Missense_Mutation_p.D1977H|SCN5A_uc021wvp.1_Missense_Mutation_p.D1978H|SCN5A_uc021wvq.1_3'UTR|SCN5A_uc021wvr.1_3'UTR|SCN5A_uc021wvs.1_3'UTR|SCN5A_uc021wvt.1_3'UTR|SCN5A_uc021wvu.1_3'UTR|SCN5A_uc021wvv.1_3'UTR|SCN5A_uc021wvj.1_Missense_Mutation_p.D1790H|SCN5A_uc021wvi.1_Missense_Mutation_p.D1844H NM_198056 NP_932173 Q14524 SCN5A_HUMAN Homo sapiens sodium channel, voltage-gated, type V, alpha subunit (SCN5A), transcript variant 1, mRNA. 1978 blood circulation|cellular response to calcium ion|muscle contraction|regulation of heart contraction sarcolemma|voltage-gated sodium channel complex protein binding|voltage-gated sodium channel activity NS(3)|breast(2)|central_nervous_system(3)|cervix(2)|endometrium(10)|haematopoietic_and_lymphoid_tissue(1)|kidney(2)|large_intestine(25)|lung(27)|ovary(6)|pancreas(3)|prostate(10)|skin(9)|upper_aerodigestive_tract(4) 107 Medulloblastoma(35;0.163) KIRC - Kidney renal clear cell carcinoma(284;0.0822)|Kidney(284;0.1) Benzonatate(DB00868)|Bepridil(DB01244)|Carbamazepine(DB00564)|Cocaine(DB00907)|Dibucaine(DB00527)|Disopyramide(DB00280)|Encainide(DB01228)|Ethotoin(DB00754)|Flecainide(DB01195)|Fosphenytoin(DB01320)|Hexylcaine(DB00473)|Indecainide(DB00192)|Lamotrigine(DB00555)|Lidocaine(DB00281)|Mephenytoin(DB00532)|Mexiletine(DB00379)|Mibefradil(DB01388)|Moricizine(DB00680)|Oxcarbazepine(DB00776)|Phenytoin(DB00252)|Prilocaine(DB00750)|Procainamide(DB01035)|Propafenone(DB01182)|Quinidine(DB00908)|Riluzole(DB00740)|Tocainide(DB01056)|Verapamil(DB00661) GTGACACTGTCATAGGAGGGT 0.602 SLC9A9 285195 broad.mit.edu 37 3 143212496 143212496 + Silent SNP T T C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr3:143212496T>C uc003evn.3 - 11 1524 c.1315_splice c.e11+1 p.G439_splice NM_173653 NP_775924 Q8IVB4 SL9A9_HUMAN Homo sapiens solute carrier family 9 (sodium/hydrogen exchanger), member 9 (SLC9A9), mRNA. 439 regulation of pH integral to membrane|late endosome membrane|recycling endosome sodium:hydrogen antiporter activity breast(2)|endometrium(5)|kidney(2)|large_intestine(13)|lung(29)|ovary(2)|skin(3)|stomach(1) 57 TTCACATACCTGAAAACATCA 0.403 KIT 3815 broad.mit.edu 37 4 55597497 55597497 + Silent SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr4:55597497C>T uc010igr.3 + 14 2232 c.2145C>T c.(2143-2145)agC>agT p.S715S KIT_uc010igs.3_Silent_p.S711S|KIT_uc010igt.2_Splice_Site_p.C163_splice NM_000222 NP_000213 P10721 KIT_HUMAN Homo sapiens v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog (KIT), transcript variant 1, mRNA. 715 Protein kinase. S -> N (in dbSNP:rs56094246). male gonad development|transmembrane receptor protein tyrosine kinase signaling pathway extracellular space|integral to membrane ATP binding|protein binding|receptor signaling protein tyrosine kinase activity p.S715del(14) NS(8)|autonomic_ganglia(1)|bone(21)|breast(2)|central_nervous_system(4)|endometrium(10)|eye(12)|genital_tract(18)|haematopoietic_and_lymphoid_tissue(1820)|kidney(17)|large_intestine(17)|lung(27)|ovary(23)|pancreas(4)|prostate(1)|salivary_gland(15)|skin(228)|soft_tissue(4117)|stomach(3)|testis(55)|thymus(7)|upper_aerodigestive_tract(1) 6411 all_cancers(7;0.00453)|all_lung(4;0.000565)|Lung NSC(11;0.00129)|all_epithelial(27;0.0104)|Glioma(25;0.08)|all_neural(26;0.101) LUSC - Lung squamous cell carcinoma(32;0.000276)|Epithelial(7;0.209) Colorectal(1;0.0276)|COAD - Colon adenocarcinoma(1;0.171) Dasatinib(DB01254)|Imatinib(DB00619)|Sorafenib(DB00398)|Sunitinib(DB01268) CTCCCAGCAGCGATAGTACTA 0.458 1 """Mis, O""" """GIST, AML, TGCT, mastocytosis, mucosal melanoma""" """GIST, epithelioma""" Piebald trait Piebaldism;Mast Cell disease, Familial Clustering of;Gastrointestinal Stromal Tumors, Sporadic Multiple Primary;Familial Gastrointestinal Stromal Tumors ARL9 132946 broad.mit.edu 37 4 57389924 57389924 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr4:57389924G>A uc003hby.1 + 3 702 c.254G>A c.(253-255)gGa>gAa p.G85E NM_206919 NP_996802 Q6T311 ARL9_HUMAN Homo sapiens ADP-ribosylation factor-like 9 (ARL9), mRNA. 149 GTP binding lung(2) 2 Glioma(25;0.08)|all_neural(26;0.101) TCTGAAGTGGGAAATGACAGG 0.433 UGT2B10 7365 broad.mit.edu 37 4 69885591 69885591 + Missense_Mutation SNP C C G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr4:69885591C>G uc011cao.1 - 2 503 c.377G>C c.(376-378)aGt>aCt p.S126T UGT2B10_uc011can.1_Intron P36537 UDB10_HUMAN Homo sapiens UDP glucuronosyltransferase 2 family, polypeptide B10 (UGT2B10), transcript variant 1, mRNA. 170 lipid metabolic process endoplasmic reticulum membrane|integral to membrane|microsome glucuronosyltransferase activity endometrium(3)|kidney(4)|large_intestine(1)|lung(13)|ovary(2)|prostate(2)|skin(3)|urinary_tract(1) 29 GAAGCTGTGACTGTACACAAA 0.408 MUC7 4589 broad.mit.edu 37 4 71346617 71346617 + Silent SNP A A G TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr4:71346617A>G uc011cat.2 + 3 444 c.156A>G c.(154-156)ctA>ctG p.L52L MUC7_uc011cau.2_Silent_p.L52L|MUC7_uc003hfj.3_Silent_p.L52L NM_001145006 NP_689504 Q8TAX7 MUC7_HUMAN Homo sapiens mucin 7, secreted (MUC7), transcript variant 1, mRNA. 52 extracellular region protein binding central_nervous_system(1)|endometrium(3)|kidney(5)|large_intestine(2)|lung(23)|ovary(3)|skin(3)|upper_aerodigestive_tract(1)|urinary_tract(1) 42 Lung(101;0.211) CTGGACTGCTAGCTCACCAGA 0.453 CARD6 84674 broad.mit.edu 37 5 40853218 40853218 + Missense_Mutation SNP T T A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr5:40853218T>A uc003jmg.3 + 2 1859 c.1784T>A c.(1783-1785)aTt>aAt p.I595N NM_032587 NP_115976 Q9BX69 CARD6_HUMAN Homo sapiens caspase recruitment domain family, member 6 (CARD6), mRNA. 595 apoptosis|regulation of apoptosis intracellular NS(1)|breast(2)|central_nervous_system(1)|endometrium(3)|haematopoietic_and_lymphoid_tissue(1)|kidney(4)|large_intestine(10)|liver(2)|lung(29)|ovary(2)|pancreas(1)|prostate(2)|skin(3)|urinary_tract(1) 62 GAGGCTCAAATTTTTCAGAGG 0.483 RGNEF 64283 broad.mit.edu 37 5 73045681 73045681 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr5:73045681C>T uc010izf.3 + 2 229 c.53C>T c.(52-54)gCg>gTg p.A18V RGNEF_uc011csq.2_Missense_Mutation_p.A18V|RGNEF_uc003kcy.1_Missense_Mutation_p.A18V|RGNEF_uc021yam.1_Missense_Mutation_p.A18V NM_001080479 NP_001073948 Q8N1W1 RGNEF_HUMAN Homo sapiens 190 kDa guanine nucleotide exchange factor (RGNEF), transcript variant 1, mRNA. 18 cell differentiation|intracellular signal transduction|regulation of Rho protein signal transduction cytoplasm|plasma membrane metal ion binding|Rho guanyl-nucleotide exchange factor activity|RNA binding Lung NSC(167;0.0378)|all_lung(232;0.04)|Ovarian(174;0.0798) OV - Ovarian serous cystadenocarcinoma(47;1.25e-51) ATGATCTATGCGAAGTTTGAC 0.443 GABRA6 2559 broad.mit.edu 37 5 161119124 161119124 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr5:161119124C>T uc003lyu.2 + 7 1342 c.1004C>T c.(1003-1005)gCc>gTc p.A335V GABRA6_uc003lyv.2_Missense_Mutation_p.A106V NM_000811 NP_000802 Q16445 GBRA6_HUMAN Homo sapiens gamma-aminobutyric acid (GABA) A receptor, alpha 6 (GABRA6), mRNA. 335 gamma-aminobutyric acid signaling pathway cell junction|chloride channel complex|integral to plasma membrane|postsynaptic membrane benzodiazepine receptor activity|chloride channel activity breast(1)|central_nervous_system(2)|endometrium(6)|large_intestine(9)|liver(2)|lung(22)|ovary(7)|skin(6)|urinary_tract(2) 57 Renal(175;0.00259) Medulloblastoma(196;0.0208)|all_neural(177;0.0672) Kidney(164;7.83e-05)|KIRC - Kidney renal clear cell carcinoma(164;0.000525) Alprazolam(DB00404)|Ethchlorvynol(DB00189)|Flunitrazepam(DB01544)|Flurazepam(DB00690)|Lorazepam(DB00186)|Meprobamate(DB00371)|Midazolam(DB00683) ACACAGAAGGCCAAAAGGAAG 0.438 TCGA Ovarian(5;0.080) TLX3 30012 broad.mit.edu 37 5 170736674 170736674 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr5:170736674C>T uc003mbf.3 + 0 387 c.305C>T c.(304-306)cCg>cTg p.P102L AX746723_uc003mbe.1_5'Flank NM_021025 NP_066305 O43711 TLX3_HUMAN Homo sapiens T-cell leukemia homeobox 3 (TLX3), mRNA. 102 nucleus sequence-specific DNA binding|sequence-specific DNA binding transcription factor activity central_nervous_system(1) 1 Renal(175;0.000159)|Lung NSC(126;0.00576)|all_lung(126;0.00963) Medulloblastoma(196;0.0399)|all_neural(177;0.0966) Kidney(164;7.24e-05)|KIRC - Kidney renal clear cell carcinoma(164;0.000516) GCCGTGCCACCGCCTCTGCCA 0.701 T BCL11B T-ALL DNAH11 8701 broad.mit.edu 37 7 21784532 21784532 + Silent SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr7:21784532C>T uc003svc.3 + 51 8413 c.8382C>T c.(8380-8382)tgC>tgT p.C2794C NM_003777 NP_003768 Q96DT5 DYH11_HUMAN Homo sapiens dynein, axonemal, heavy chain 11 (DNAH11), mRNA. 2794 microtubule-based movement axonemal dynein complex|cilium axoneme|cytoplasm|microtubule ATP binding|ATPase activity|microtubule motor activity NS(1)|autonomic_ganglia(1)|breast(13)|central_nervous_system(3)|cervix(4)|endometrium(18)|haematopoietic_and_lymphoid_tissue(1)|kidney(9)|large_intestine(50)|lung(101)|ovary(10)|pancreas(4)|prostate(7)|skin(3)|stomach(2)|upper_aerodigestive_tract(1)|urinary_tract(2) 230 TCATTTATTGCCACTTTGCTG 0.448 Kartagener syndrome PRSS3P2 154754 broad.mit.edu 37 7 142481888 142481888 + Silent SNP T T C rs138077672 by1000genomes TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr7:142481888T>C uc011ksq.2 + 3 650 c.567T>C c.(565-567)ctT>ctC p.L189L TCRBV2S1_uc003vzp.2_Intron|TCRBV3S1_uc011ksh.2_Intron|TCRBV3S1_uc003vzw.2_Intron|TCRBV3S1_uc011ksi.2_Intron|TCRBV3S1_uc010loj.2_Intron|TCRBV3S1_uc003wag.2_Intron|BV6S4-BJ2S2_uc003wan.1_Intron Homo sapiens protease, serine, 3 pseudogene (TRY6), non-coding RNA. TGGGCTTCCTTGAGGGAGGCA 0.522 OR6V1 346517 broad.mit.edu 37 7 142749846 142749846 + Missense_Mutation SNP G G T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr7:142749846G>T uc011ksv.2 + 0 409 c.409G>T c.(409-411)Gct>Tct p.A137S NM_001001667 NP_001001667 Q8N148 OR6V1_HUMAN Homo sapiens olfactory receptor, family 6, subfamily V, member 1 (OR6V1), mRNA. 137 sensory perception of smell integral to membrane|plasma membrane olfactory receptor activity endometrium(2)|kidney(2)|large_intestine(1)|lung(13)|ovary(1)|upper_aerodigestive_tract(1) 20 Melanoma(164;0.059) GATGAGCCGGGCTATGTGTGT 0.597 TEX15 56154 broad.mit.edu 37 8 30695499 30695499 + Silent SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr8:30695499C>T uc003xil.3 - 2 7152 c.7152G>A c.(7150-7152)acG>acA p.T2384T NM_031271 NP_112561 Q9BXT5 TEX15_HUMAN Homo sapiens testis expressed 15 (TEX15), mRNA. 2384 NS(2)|breast(3)|cervix(5)|endometrium(7)|haematopoietic_and_lymphoid_tissue(1)|kidney(5)|large_intestine(38)|lung(56)|ovary(5)|pancreas(1)|prostate(2)|skin(7)|upper_aerodigestive_tract(5)|urinary_tract(1) 138 KIRC - Kidney renal clear cell carcinoma(542;0.0918)|Kidney(114;0.111) CCTTTTTTGGCGTTAAATGAT 0.388 GPR124 25960 broad.mit.edu 37 8 37697018 37697018 + Missense_Mutation SNP T T C TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr8:37697018T>C uc003xkj.3 + 16 2774 c.2388_splice c.e16-1 p.S796_splice GPR124_uc010lvy.3_Splice_Site_p.S579_splice NM_032777 NP_116166 Q96PE1 GP124_HUMAN Homo sapiens G protein-coupled receptor 124 (GPR124), mRNA. 796 central nervous system development|endothelial cell migration|neuropeptide signaling pathway|regulation of angiogenesis|regulation of chemotaxis|sprouting angiogenesis integral to membrane|plasma membrane G-protein coupled receptor activity central_nervous_system(1)|endometrium(5)|kidney(3)|large_intestine(4)|lung(16)|ovary(4)|skin(2)|stomach(1)|upper_aerodigestive_tract(1) 37 BRCA - Breast invasive adenocarcinoma(5;2.75e-24)|LUSC - Lung squamous cell carcinoma(8;3.5e-10) TCCGGGCAGCTCCATCCGTGT 0.592 TBC1D2 55357 broad.mit.edu 37 9 101014108 101014108 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr9:101014108G>A uc011lvb.2 - 1 650 c.470C>T c.(469-471)gCc>gTc p.A157V TBC1D2_uc004ayq.3_Missense_Mutation_p.A157V|TBC1D2_uc004ayr.3_Intron NM_018421 NP_060891 Q9BYX2 TBD2A_HUMAN Homo sapiens TBC1 domain family, member 2 (TBC1D2), mRNA. 157 Interaction with CADH1. cell junction|cytoplasmic membrane-bounded vesicle|nucleus Rab GTPase activator activity breast(1)|endometrium(5)|kidney(2)|large_intestine(7)|ovary(3)|prostate(4)|skin(1)|upper_aerodigestive_tract(1) 24 Myeloproliferative disorder(762;0.0255) OV - Ovarian serous cystadenocarcinoma(323;2.55e-37) AGCCAGGGCGGCATCAGGGGT 0.637 TTLL11 158135 broad.mit.edu 37 9 124751932 124751932 + Missense_Mutation SNP C C T TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr9:124751932C>T uc011lyl.2 - 3 1269 c.1081G>A c.(1081-1083)Gca>Aca p.A361T TTLL11_uc004blr.3_Non-coding_Transcript|TTLL11_uc011lym.1_Missense_Mutation_p.A38T|TTLL11_uc004blt.1_Missense_Mutation_p.A361T|TTLL11_uc004blu.1_3'UTR NM_001139442 NP_001132914 Q8NHH1 TTL11_HUMAN Homo sapiens tubulin tyrosine ligase-like family, member 11 (TTLL11), transcript variant 1, mRNA. 361 TTL. protein modification process cilium|microtubule basal body tubulin-tyrosine ligase activity breast(1)|endometrium(1)|kidney(1)|large_intestine(6)|lung(5)|prostate(3)|skin(1) 18 AGGGTCCCTGCCAGGCGGATG 0.517 TTLL11 158135 broad.mit.edu 37 9 124794081 124794081 + Missense_Mutation SNP T T A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 Untested Somatic Phase_I WXS none Illumina GAIIx 2fdab641-d73b-4f9a-aa4c-c1944f131a69 0f88c693-5a30-43b1-be9e-c96a791d984c g.chr9:124794081T>A uc011lyl.2 - 2 1072 c.884A>T c.(883-885)cAg>cTg p.Q295L TTLL11_uc004blr.3_Intron|TTLL11_uc011lym.1_Intron|TTLL11_uc004blt.1_Missense_Mutation_p.Q295L|TTLL11_uc004blu.1_Intron NM_001139442 NP_001132914 Q8NHH1 TTL11_HUMAN Homo sapiens tubulin tyrosine ligase-like family, member 11 (TTLL11), transcript variant 1, mRNA. 295 TTL. protein modification process cilium|microtubule basal body tubulin-tyrosine ligase activity p.Q295Q(1) breast(1)|endometrium(1)|kidney(1)|large_intestine(6)|lung(5)|prostate(3)|skin(1) 18 AAAGAGATTCTGCATGGTTCT 0.507