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 chromosome_name start stop reference variant type gene_name transcript_name transcript_species transcript_source transcript_version strand transcript_status trv_type c_position amino_acid_change ucsc_cons domain all_domains deletion_substructures transcript_error rsID rsID_ref_var_alleles CAF normal_ref_reads normal_var_reads normal_vaf tumor_ref_reads tumor_var_reads tumor_vaf normal_ref_reads_val normal_var_reads_val normal_vaf_val tumor_ref_reads_val tumor_var_reads_val tumor_vaf_val AK5 0 genome.wustl.edu 37 1 77876675 77876675 + Missense_Mutation SNP G G A TCGA-X7-A8DI-01A-11D-A423-09 TCGA-X7-A8DI-10A-01D-A426-09 G G G A G G Unknown Valid Somatic Phase_IV WXS Hybrid_Capture_Illumina_Seq Illumina HiSeq c6f718ae-772d-43b5-8855-2c44b375d61e 8a785b6e-4abe-4c94-8e68-55b39e06c0b5 1 77876675 77876675 G A SNP AK5 ENST00000354567 human ensembl 74_37 1 known missense c.901 p.D301N 1 superfamily_P-loop_NTPase pfam_Adenylate_kin,pfam_Dpy-30_motif,superfamily_P-loop_NTPase,superfamily_cAMP_dep_PK_reg_su_I/II_a/b,prints_Adenylate_kin,tigrfam_Adenylate_kin1 0 no_errors 0 0 0 53 0 0 74 6 7.5 325 0 0.00 180 14 7.22 CCNL1 0 genome.wustl.edu 37 3 156876755 156876755 + Missense_Mutation SNP T T C TCGA-X7-A8DI-01A-11D-A423-09 TCGA-X7-A8DI-10A-01D-A426-09 T T T C T T Unknown Valid Somatic Phase_IV WXS Hybrid_Capture_Illumina_Seq Illumina HiSeq c6f718ae-772d-43b5-8855-2c44b375d61e 8a785b6e-4abe-4c94-8e68-55b39e06c0b5 3 156876755 156876755 T C SNP CCNL1 ENST00000295926 human ensembl 74_37 -1 known missense c.388 p.M130V 1 pfam_Cyclin_N,superfamily_Cyclin-like,smart_Cyclin-like,pirsf_Cyclin_L pfam_Cyclin_N,superfamily_Cyclin-like,smart_Cyclin-like,pirsf_Cyclin_L 0 no_errors 0 0 0 32 0 0 57 7 10.94 376 0 0.00 220 14 5.96 UGT2B4 0 genome.wustl.edu 37 4 70361046 70361046 + Silent SNP G G A TCGA-X7-A8DI-01A-11D-A423-09 TCGA-X7-A8DI-10A-01D-A426-09 G G G A G G Unknown Valid Somatic Phase_IV WXS Hybrid_Capture_Illumina_Seq Illumina HiSeq c6f718ae-772d-43b5-8855-2c44b375d61e 8a785b6e-4abe-4c94-8e68-55b39e06c0b5 4 70361046 70361046 G A SNP UGT2B4 ENST00000305107 human ensembl 74_37 -1 known silent c.534 p.Y178 0 pfam_UDP_glucos_trans pfam_UDP_glucos_trans,pfam_Glyco_trans_28_C 0 no_errors rs370531105 G->A 0 51 0 0 67 7 9.46 238 0 0.00 173 14 7.45 GTF2I 0 genome.wustl.edu 37 7 74146970 74146970 + Missense_Mutation SNP T T A TCGA-X7-A8DI-01A-11D-A423-09 TCGA-X7-A8DI-10A-01D-A426-09 T T T A T T Unknown Valid Somatic Phase_IV WXS Hybrid_Capture_Illumina_Seq Illumina HiSeq c6f718ae-772d-43b5-8855-2c44b375d61e 8a785b6e-4abe-4c94-8e68-55b39e06c0b5 7 74146970 74146970 T A SNP GTF2I ENST00000324896 human ensembl 74_37 1 known missense c.1271 p.L424H 1 pfam_GTF2I,superfamily_GTF2I,pirsf_TF_II-I,pfscan_GTF2I pfam_GTF2I,superfamily_GTF2I,pirsf_TF_II-I,pfscan_GTF2I 0 no_errors 0 0 0 309 0 0 415 37 8.19 204 0 0.00 130 7 5.04 CDH20 0 genome.wustl.edu 37 18 59206323 59206323 + Missense_Mutation SNP C C A TCGA-X7-A8DI-01A-11D-A423-09 TCGA-X7-A8DI-10A-01D-A426-09 C C C A C C Unknown Valid Somatic Phase_IV WXS Hybrid_Capture_Illumina_Seq Illumina HiSeq c6f718ae-772d-43b5-8855-2c44b375d61e 8a785b6e-4abe-4c94-8e68-55b39e06c0b5 18 59206323 59206323 C A SNP CDH20 ENST00000262717 human ensembl 74_37 1 known missense c.1475 p.P492Q 1 superfamily_Cadherin-like,smart_Cadherin,pfscan_Cadherin,prints_Cadherin pfam_Cadherin,pfam_Cadherin_cytoplasmic-dom,superfamily_Cadherin-like,smart_Cadherin,pfscan_Cadherin,prints_Cadherin 0 no_errors 0 0 0 105 0 0 106 12 10.17 337 0 0.00 238 16 6.30