ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-250 REPIN1 SNP Missense_Mutation 7 150069904 G A 34 54 LUAD LUAD-E01217 REPIN1 SNP Missense_Mutation 7 150069696 G T 37 76 LUAD LUAD-RT-S01769 REPIN1 SNP Missense_Mutation 7 150069216 G C 33 70 MEL ME044 REPIN1 SNP Missense_Mutation 7 150069694 C T 22 66 MEL MEL-JWCI-WGS-4 REPIN1 SNP Silent 7 150069707 C T 31 59 MEL MEL-Ma-Mel-67 REPIN1 SNP Missense_Mutation 7 150069607 C T 30 78 GBM TCGA-06-0140 REPIN1 SNP Missense_Mutation 7 150068350 G A 35 64 GBM TCGA-06-0210 REPIN1 SNP Missense_Mutation 7 150069796 G T 46 91 GBM TCGA-06-0211 REPIN1 SNP Silent 7 150069659 C A 25 45 GBM TCGA-19-5959 REPIN1 SNP Silent 7 150069842 G A 38 46 LUSC TCGA-22-5472 REPIN1 SNP Missense_Mutation 7 150069192 G T 39 93 OV TCGA-24-1564 REPIN1 SNP Missense_Mutation 7 150068781 G A 37 64 GBM TCGA-28-5219 REPIN1 SNP Missense_Mutation 7 150068992 C T 27 53 GBM TCGA-32-2491 REPIN1 SNP Missense_Mutation 7 150069637 G T 46 90 LUSC TCGA-34-5927 REPIN1 SNP Missense_Mutation 7 150069034 C A 22 59 LUSC TCGA-37-4141 REPIN1 SNP Silent 7 150069554 C T 27 52 LUAD TCGA-44-6144 REPIN1 SNP Missense_Mutation 7 150069234 C T 23 58 LUSC TCGA-60-2707 REPIN1 SNP Nonsense_Mutation 7 150069612 G T 37 77 LUAD TCGA-75-5126 REPIN1 SNP Missense_Mutation 7 150069696 G A 37 76 GBM TCGA-76-6662 REPIN1 SNP Missense_Mutation 7 150069247 A G 2 72 UCEC TCGA-AP-A0LM REPIN1 SNP Missense_Mutation 7 150069673 C T 27 57 KIRC TCGA-B0-4841 REPIN1 SNP Missense_Mutation 7 150066808 T C 49 62 UCEC TCGA-BS-A0UV REPIN1 SNP Missense_Mutation 7 150066870 A G 3 60 HNSC TCGA-CV-7409 REPIN1 SNP Missense_Mutation 7 150069096 C T 23 62 BLCA TCGA-G2-A3IE REPIN1 SNP Silent 7 150068792 C T 32 58