ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-MAYO_DLBCL_234 TPCN2 SNP Missense_Mutation 11 68835056 C T 19 80 LUAD LUAD-5V8LT TPCN2 SNP Silent 11 68825057 C T 31 23 LUAD LUAD-B00631 TPCN2 SNP Silent 11 68854030 G A 40 51 LUAD LUAD-B01024 TPCN2 SNP Silent 11 68846371 C T 27 49 LUAD LUAD-B02515 TPCN2 SNP Splice_site 11 68822819 A T 3 85 LUAD LUAD-S01467 TPCN2 SNP Missense_Mutation 11 68839427 G A 43 89 MEL MEL-Ma-Mel-105 TPCN2 SNP Missense_Mutation 11 68837924 C T 23 63 MEL MEL-Ma-Mel-114 TPCN2 SNP Silent 11 68848931 C T 31 48 MM MM-0579 TPCN2 SNP Silent 11 68852722 A G 11 43 LUAD TCGA-05-4395 TPCN2 SNP Missense_Mutation 11 68835056 C T 19 80 LUAD TCGA-05-4396 TPCN2 SNP Missense_Mutation 11 68830359 G T 39 90 GBM TCGA-06-0119 TPCN2 SNP Missense_Mutation 11 68854047 A G 2 78 GBM TCGA-06-0128 TPCN2 SNP Silent 11 68822263 A G 2 51 LUSC TCGA-18-3409 TPCN2 SNP Missense_Mutation 11 68822765 C A 18 92 LUSC TCGA-22-4593 TPCN2 SNP Missense_Mutation 11 68848948 G A 40 73 LUSC TCGA-33-6737 TPCN2 SNP Silent 11 68851475 G A 41 63 LUAD TCGA-35-3621 TPCN2 SNP Silent 11 68822766 C T 23 21 LUSC TCGA-43-5668 TPCN2 SNP Silent 11 68838835 C T 32 64 LUSC TCGA-46-3765 TPCN2 SNP Missense_Mutation 11 68840410 C T 28 53 LUSC TCGA-60-2698 TPCN2 SNP Missense_Mutation 11 68851471 G A 42 69 LUSC TCGA-66-2785 TPCN2 SNP Silent 11 68855388 G A 45 52 LUAD TCGA-75-5126 TPCN2 SNP Silent 11 68846407 C T 29 57 LUSC TCGA-85-6561 TPCN2 SNP Missense_Mutation 11 68822717 C A 27 79 CRC TCGA-AA-3516 TPCN2 SNP Missense_Mutation 11 68825058 G A 39 88 CRC TCGA-AA-3672 TPCN2 SNP Missense_Mutation 11 68854064 A G 12 59 CRC TCGA-AA-3864 TPCN2 SNP Silent 11 68840442 C T 19 35 CRC TCGA-AA-A00J TPCN2 DEL In_Frame_Del 11 68846390 CTG - 24 46 CRC TCGA-AA-A00J TPCN2 SNP Missense_Mutation 11 68846395 G T 47 56 CRC TCGA-AA-A00K TPCN2 SNP Missense_Mutation 11 68846256 C G 24 50 CRC TCGA-AA-A010 TPCN2 SNP Silent 11 68830441 G A 38 48 AML TCGA-AB-2828 TPCN2 SNP Silent 11 68854603 C A 22 50 UCEC TCGA-AP-A059 TPCN2 SNP Missense_Mutation 11 68838829 C A 24 53 UCEC TCGA-AP-A059 TPCN2 SNP Missense_Mutation 11 68848947 C T 27 65 UCEC TCGA-AP-A059 TPCN2 SNP Missense_Mutation 11 68851471 G A 42 69 UCEC TCGA-AP-A0LM TPCN2 SNP Missense_Mutation 11 68821551 G A 37 86 UCEC TCGA-AP-A0LM TPCN2 SNP Missense_Mutation 11 68851462 G A 40 70 UCEC TCGA-AX-A0J1 TPCN2 SNP Silent 11 68822733 C T 27 43 UCEC TCGA-AX-A0J1 TPCN2 SNP Missense_Mutation 11 68852697 C T 26 83 UCEC TCGA-B5-A11E TPCN2 SNP Missense_Mutation 11 68830358 C T 27 65 KIRC TCGA-BP-4995 TPCN2 SNP Splice_Site 11 68853399 G A 40 72 UCEC TCGA-BS-A0UV TPCN2 SNP Silent 11 68831408 C T 31 41 HNSC TCGA-CN-5360 TPCN2 SNP Silent 11 68830381 C A 24 53 HNSC TCGA-CN-5369 TPCN2 SNP Missense_Mutation 11 68846367 A G 2 62 HNSC TCGA-CR-7404 TPCN2 SNP Missense_Mutation 11 68822767 G A 37 71 HNSC TCGA-CV-7418 TPCN2 SNP Missense_Mutation 11 68835058 G A 42 67 HNSC TCGA-CV-7423 TPCN2 SNP Splice_Site 11 68822187 A G 15 82 UCEC TCGA-D1-A103 TPCN2 SNP Silent 11 68846006 C T 31 52 BLCA TCGA-DK-A1A3 TPCN2 SNP Missense_Mutation 11 68838874 C T 23 65 HNSC TCGA-DQ-7592 TPCN2 SNP Silent 11 68846464 C T 19 48 BRCA TCGA-E2-A15S TPCN2 SNP Missense_Mutation 11 68825062 G C 47 75