ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0054 SH3RF3 SNP Silent 2 110015348 C T 23 38 DLBCL DLBCL-MAYO_DLBCL_234 SH3RF3 SNP Missense_Mutation 2 109964230 G A 38 70 ESO ESO-721 SH3RF3 SNP Missense_Mutation 2 110053471 C G 18 51 LUAD LUAD-5V8LT SH3RF3 SNP Missense_Mutation 2 109964229 C A 27 84 LUAD LUAD-CHTN-MAD06-00668 SH3RF3 SNP Silent 2 109964285 C T 30 57 LUAD LUAD-S01315 SH3RF3 SNP Missense_Mutation 2 110259193 T A 55 75 MEL MEL-Ma-Mel-37 SH3RF3 SNP Missense_Mutation 2 110065782 C T 21 64 MM MM-0450 SH3RF3 SNP Missense_Mutation 2 110259087 G A 40 99 MM MM-0460 SH3RF3 SNP Missense_Mutation 2 109964332 C T 22 94 MM MM-0605 SH3RF3 SNP Missense_Mutation 2 110259165 C T 27 57 LUAD TCGA-05-4382 SH3RF3 SNP Missense_Mutation 2 109964320 C G 21 94 GBM TCGA-06-6693 SH3RF3 SNP Missense_Mutation 2 110015136 G A 39 53 OV TCGA-13-1510 SH3RF3 SNP Silent 2 109964324 C T 19 50 LUAD TCGA-17-Z020 SH3RF3 SNP Missense_Mutation 2 110015211 G A 41 95 OV TCGA-24-1470 SH3RF3 SNP Silent 2 109964171 C T 19 35 LUSC TCGA-33-4566 SH3RF3 SNP Missense_Mutation 2 110015230 A T 3 87 LUSC TCGA-46-3769 SH3RF3 SNP Missense_Mutation 2 110049062 G C 35 66 LUAD TCGA-67-3771 SH3RF3 SNP Silent 2 110048969 C G 32 49 CRC TCGA-AA-3710 SH3RF3 SNP Missense_Mutation 2 110259085 G A 38 84 CRC TCGA-AA-3977 SH3RF3 SNP Silent 2 110048996 C T 19 45 CRC TCGA-AA-3977 SH3RF3 SNP Silent 2 110259086 C T 27 33 CRC TCGA-AA-A010 SH3RF3 SNP Missense_Mutation 2 109964319 C T 26 66 CRC TCGA-AA-A01R SH3RF3 SNP Missense_Mutation 2 109964226 C T 27 76 CRC TCGA-AG-A02N SH3RF3 SNP Missense_Mutation 2 110065656 G A 39 72 UCEC TCGA-AP-A056 SH3RF3 SNP Silent 2 110259140 C T 27 25 UCEC TCGA-AP-A059 SH3RF3 SNP Missense_Mutation 2 110065767 C T 23 59 UCEC TCGA-AP-A059 SH3RF3 SNP Missense_Mutation 2 110259198 C T 27 51 UCEC TCGA-AP-A0LH SH3RF3 INS Frame_Shift_Ins 2 110259240 - T 11 86 UCEC TCGA-AP-A0LM SH3RF3 SNP Silent 2 109964258 C T 27 31 UCEC TCGA-AP-A0LM SH3RF3 SNP Silent 2 110259125 C T 31 43 UCEC TCGA-B5-A11E SH3RF3 SNP Silent 2 110107252 C T 27 46 KIRC TCGA-BP-4992 SH3RF3 SNP Silent 2 110053415 G T 41 41 UCEC TCGA-BS-A0UF SH3RF3 SNP Missense_Mutation 2 110048973 G A 38 69 UCEC TCGA-BS-A0UF SH3RF3 SNP Missense_Mutation 2 110048997 G A 37 99 UCEC TCGA-BS-A0UV SH3RF3 SNP Silent 2 110107342 G A 38 49 HNSC TCGA-CN-5356 SH3RF3 INS Frame_Shift_Ins 2 110036087 - T 46 50 HNSC TCGA-CR-7388 SH3RF3 SNP Silent 2 109988086 G T 39 26 HNSC TCGA-CV-5973 SH3RF3 SNP Silent 2 109964267 C T 19 46 HNSC TCGA-CV-6939 SH3RF3 SNP Missense_Mutation 2 110053585 G C 39 82 HNSC TCGA-CV-6959 SH3RF3 SNP Missense_Mutation 2 110015235 C T 19 81 HNSC TCGA-CX-7082 SH3RF3 SNP Missense_Mutation 2 110015122 T G 55 65 UCEC TCGA-D1-A0ZS SH3RF3 SNP Missense_Mutation 2 110015380 C T 31 96 UCEC TCGA-D1-A103 SH3RF3 SNP Missense_Mutation 2 110015330 C A 28 74 UCEC TCGA-D1-A177 SH3RF3 SNP Missense_Mutation 2 109746024 G A 38 53 BLCA TCGA-DK-A1AG SH3RF3 SNP Missense_Mutation 2 110015235 C T 19 81