ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0043 RBM11 SNP Nonsense_Mutation 21 15599435 G T 45 75 BRCA BR-MEX-095 RBM11 SNP Silent 21 15599275 C G 23 42 ESO ESO-051 RBM11 SNP Missense_Mutation 21 15599429 G A 33 57 HNSC HN_62646 RBM11 SNP Missense 21 15599508 G A 37 63 LUAD LUAD-B00416 RBM11 SNP Silent 21 15588565 C A 23 64 MEL MEL-JWCI-14 RBM11 SNP Splice_site 21 15593418 G A 43 80 MEL MEL-JWCI-WGS-4 RBM11 SNP Missense_Mutation 21 15599294 C T 29 60 MEL MEL-Ma-Mel-119 RBM11 SNP Missense_Mutation 21 15596808 C T 30 60 MEL MEL-UKRV-Mel-6 RBM11 SNP Missense_Mutation 21 15599501 A G 9 63 LUAD TCGA-17-Z033 RBM11 SNP Missense_Mutation 21 15599378 G T 34 55 LUSC TCGA-34-5236 RBM11 SNP Missense_Mutation 21 15599537 G C 45 70 LUSC TCGA-43-6770 RBM11 SNP Silent 21 15591904 G C 45 58 LUAD TCGA-44-6779 RBM11 SNP Splice_Site 21 15596757 A C 3 75 LUSC TCGA-60-2698 RBM11 SNP Missense_Mutation 21 15599481 A G 10 75 LUSC TCGA-66-2759 RBM11 SNP Missense_Mutation 21 15591942 T C 64 82 LUSC TCGA-70-6722 RBM11 SNP Missense_Mutation 21 15599595 A G 3 76 AML TCGA-AB-2806 RBM11 SNP Missense_Mutation 21 15599511 A T 3 77 KIRC TCGA-AK-3436 RBM11 SNP Missense_Mutation 21 15592035 A T 7 70 UCEC TCGA-AP-A051 RBM11 SNP Missense_Mutation 21 15599204 T C 59 58 UCEC TCGA-AP-A051 RBM11 SNP Missense_Mutation 21 15599549 G T 33 82 UCEC TCGA-AP-A056 RBM11 SNP Missense_Mutation 21 15599384 C T 20 74 UCEC TCGA-AP-A059 RBM11 SNP Missense_Mutation 21 15591978 C A 32 89 UCEC TCGA-AX-A05Z RBM11 SNP Missense_Mutation 21 15599387 C A 30 52 KIRC TCGA-B0-5705 RBM11 SNP Nonsense_Mutation 21 15599585 C T 23 55 BLCA TCGA-BT-A20R RBM11 SNP Missense_Mutation 21 15588577 G A 33 87 HNSC TCGA-CV-6945 RBM11 SNP Missense_Mutation 21 15599316 G C 41 67 HNSC TCGA-CV-6945 RBM11 SNP Missense_Mutation 21 15599442 G C 41 68 HNSC TCGA-CV-6945 RBM11 SNP Missense_Mutation 21 15599531 G A 45 82 HNSC TCGA-CV-6945 RBM11 SNP Nonsense_Mutation 21 15599567 G T 37 70 HNSC TCGA-CV-6945 RBM11 SNP Silent 21 15599599 G A 33 49 UCEC TCGA-D1-A16F RBM11 SNP Missense_Mutation 21 15588530 C T 26 67 UCEC TCGA-D1-A16N RBM11 SNP Nonsense_Mutation 21 15599471 C T 17 76 BLCA TCGA-DK-A1AC RBM11 SNP Silent 21 15599290 G A 45 41 BLCA TCGA-DK-A1AC RBM11 SNP Silent 21 15599416 G A 45 42