ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MED MD-296 RNF38 SNP Missense_Mutation 9 36369725 T C 57 53 MEL MEL-Ma-Mel-102 RNF38 SNP Missense_Mutation 9 36369843 G A 35 65 MM MM-0329 RNF38 SNP Silent 9 36352762 A G 12 67 LUAD TCGA-17-Z016 RNF38 SNP Missense_Mutation 9 36356416 G A 44 80 LUAD TCGA-44-2661 RNF38 SNP Missense_Mutation 9 36353229 G C 41 94 LUAD TCGA-73-4668 RNF38 SNP Missense_Mutation 9 36356463 T A 55 65 BRCA TCGA-A8-A075 RNF38 SNP Silent 9 36344831 A G 3 53 CRC TCGA-AA-A010 RNF38 SNP Missense_Mutation 9 36357936 G T 47 94 AML TCGA-AB-2854 RNF38 SNP Missense_Mutation 9 36369846 A G 11 74 UCEC TCGA-AP-A051 RNF38 SNP Silent 9 36357880 A G 9 51 UCEC TCGA-AP-A059 RNF38 SNP Missense_Mutation 9 36376030 G A 47 95 UCEC TCGA-AP-A0LM RNF38 SNP Missense_Mutation 9 36344890 C A 32 95 UCEC TCGA-AX-A0J1 RNF38 SNP Missense_Mutation 9 36352809 G A 40 95 UCEC TCGA-AX-A0J1 RNF38 SNP Missense_Mutation 9 36376094 G A 38 65 CRC TCGA-AY-4071 RNF38 SNP Splice_site 9 36369716 C T 24 94 KIRC TCGA-B0-4827 RNF38 SNP Missense_Mutation 9 36376116 A T 16 62 UCEC TCGA-B5-A0JY RNF38 SNP Nonsense_Mutation 9 36375992 G A 37 81 UCEC TCGA-B5-A11E RNF38 SNP Missense_Mutation 9 36342359 T C 59 86 UCEC TCGA-B5-A11N RNF38 SNP Missense_Mutation 9 36353262 A C 13 86 UCEC TCGA-BS-A0UF RNF38 SNP Missense_Mutation 9 36351148 T A 52 54 UCEC TCGA-BS-A0UF RNF38 SNP Missense_Mutation 9 36353177 G A 41 91 UCEC TCGA-BS-A0UJ RNF38 SNP Missense_Mutation 9 36357786 T C 53 70 UCEC TCGA-D1-A103 RNF38 SNP Missense_Mutation 9 36356413 G T 35 80 UCEC TCGA-D1-A167 RNF38 SNP Missense_Mutation 9 36376031 G A 44 95 UCEC TCGA-D1-A16X RNF38 SNP Silent 9 36351115 G A 40 49 CARC Carc-BWH11 RNF38 SNP Missense_Mutation 9 36376094 G T 38 65