ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-191 LSM14B SNP Missense_Mutation 20 60704899 G T 33 74 ESO ESO-021 LSM14B SNP Splice_site 20 60705587 A G 9 56 LUAD LUAD-B00731 LSM14B SNP Missense_Mutation 20 60708389 G C 33 95 MEL ME016 LSM14B SNP Silent 20 60701420 C A 23 50 MEL MEL-Ma-Mel-102 LSM14B SNP Missense_Mutation 20 60704852 C T 30 81 LUAD TCGA-05-4396 LSM14B SNP Missense_Mutation 20 60699814 C A 23 77 GBM TCGA-06-0878 LSM14B SNP Missense_Mutation 20 60697790 G A 38 90 LUAD TCGA-17-Z018 LSM14B SNP Missense_Mutation 20 60706504 T A 55 67 LUSC TCGA-43-6143 LSM14B SNP Missense_Mutation 20 60701381 G T 38 52 LUSC TCGA-66-2800 LSM14B SNP Silent 20 60699680 C T 24 54 CRC TCGA-AA-3811 LSM14B SNP Missense_Mutation 20 60708368 G A 37 95 BRCA TCGA-AN-A04D LSM14B SNP Missense_Mutation 20 60708435 G C 39 67 BRCA TCGA-AO-A124 LSM14B SNP Silent 20 60705737 G T 45 56 UCEC TCGA-AP-A051 LSM14B SNP Missense_Mutation 20 60706442 A G 10 89 UCEC TCGA-AP-A059 LSM14B SNP Silent 20 60701386 G A 38 51 UCEC TCGA-AP-A059 LSM14B SNP Missense_Mutation 20 60704910 C A 28 57 UCEC TCGA-AP-A059 LSM14B SNP Missense_Mutation 20 60705000 C T 19 59 UCEC TCGA-AP-A059 LSM14B SNP Missense_Mutation 20 60706415 A G 10 75 UCEC TCGA-AP-A0LM LSM14B SNP Nonsense_Mutation 20 60708446 C T 23 71 UCEC TCGA-AP-A0LP LSM14B SNP Nonsense_Mutation 20 60705594 C T 27 56 BRCA TCGA-AR-A251 LSM14B SNP Missense_Mutation 20 60699699 C T 30 84 UCEC TCGA-AX-A05Z LSM14B SNP Silent 20 60705677 C T 31 65 HNSC TCGA-CV-6961 LSM14B SNP Missense_Mutation 20 60706468 G A 37 88 KIRC TCGA-CZ-4858 LSM14B SNP Missense_Mutation 20 60705681 A G 11 69 KIRC TCGA-CZ-4865 LSM14B SNP Missense_Mutation 20 60708449 G A 35 95 UCEC TCGA-D1-A103 LSM14B SNP Missense_Mutation 20 60705625 G A 40 100 UCEC TCGA-D1-A169 LSM14B SNP Silent 20 60701479 C T 23 34 UCEC TCGA-D1-A177 LSM14B SNP Missense_Mutation 20 60705329 G A 33 86 UCEC TCGA-D1-A17Q LSM14B SNP Silent 20 60705677 C T 31 65 BRCA TCGA-E9-A1N5 LSM14B SNP Missense_Mutation 20 60701300 G A 45 53 BRCA TCGA-E9-A1RH LSM14B SNP Missense_Mutation 20 60706418 A T 3 63 KIRC TCGA-EU-5905 LSM14B SNP Missense_Mutation 20 60701436 A G 14 77 BLCA TCGA-G2-A2EK LSM14B SNP Missense_Mutation 20 60697745 C T 23 76 BLCA TCGA-HQ-A2OE LSM14B SNP Missense_Mutation 20 60706547 C T 32 84