ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-085 RNLS SNP Silent 10 90342876 C T 19 63 MEL MEL-Ma-Mel-114 RNLS SNP Silent 10 90074376 G A 43 49 LUAD TCGA-05-4389 RNLS SNP Missense_Mutation 10 90332672 C A 29 89 OV TCGA-10-0935 RNLS SNP Missense_Mutation 10 90122431 C G 31 90 LUAD TCGA-91-6829 RNLS SNP Missense_Mutation 10 90341368 G A 35 86 UCEC TCGA-AP-A051 RNLS SNP Nonsense_Mutation 10 90332760 C T 22 75 UCEC TCGA-AP-A059 RNLS SNP Missense_Mutation 10 90034779 G T 34 53 UCEC TCGA-AP-A0LM RNLS SNP Splice_site 10 90074397 C A 20 50 UCEC TCGA-AP-A0LM RNLS SNP Missense_Mutation 10 90122419 C T 26 90 BRCA TCGA-AQ-A04L RNLS SNP Nonsense_Mutation 10 90122432 G A 37 90 UCEC TCGA-AX-A0J1 RNLS SNP Missense_Mutation 10 90034737 G A 38 49 UCEC TCGA-B5-A0JY RNLS SNP Silent 10 90034736 C T 31 43 UCEC TCGA-B5-A11E RNLS SNP Nonsense_Mutation 10 90074235 C T 30 94 BRCA TCGA-B6-A0RO RNLS DEL In_Frame_Del 10 90332770 TCT - 50 63 BRCA TCGA-BH-A0HK RNLS SNP Silent 10 90341439 G A 38 42 UCEC TCGA-BS-A0UF RNLS SNP Missense_Mutation 10 90342837 C A 24 49 KIRC TCGA-CJ-5675 RNLS SNP Missense_Mutation 10 90122392 A G 4 71 HNSC TCGA-CN-4739 RNLS SNP Silent 10 90122454 C T 21 69 HNSC TCGA-CV-6943 RNLS SNP Missense_Mutation 10 90034742 C T 29 52 UCEC TCGA-D1-A103 RNLS SNP Silent 10 90122415 G T 33 62 HNSC TCGA-DQ-7595 RNLS SNP Missense_Mutation 10 90122434 G T 33 68