ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1757 RINT1 SNP Nonsense_Mutation 7 105192070 C T 25 99 DLBCL DLBCL-Ls1899 RINT1 SNP Missense_Mutation 7 105204310 G A 40 84 HNSC HN_62739 RINT1 SNP Missense 7 105206086 A T 16 76 LUAD LUAD-CHTN-Z4716A RINT1 SNP Missense_Mutation 7 105189045 C G 32 62 LUAD LUAD-E00918 RINT1 SNP Missense_Mutation 7 105187728 A C 12 46 LUAD LUAD-S01468 RINT1 SNP Silent 7 105192138 A C 14 46 MEL ME009 RINT1 SNP Splice_Site 7 105207565 G A 36 97 MEL ME032 RINT1 SNP Silent 7 105190573 G A 34 57 MEL MEL-JWCI-WGS-12 RINT1 SNP Splice_site 7 105187780 C T 31 99 MEL MEL-JWCI-WGS-3 RINT1 SNP Missense_Mutation 7 105182879 C T 30 86 MM MM-0004 RINT1 SNP Missense_Mutation 7 105204214 T G 59 89 MM MM-0460 RINT1 SNP Missense_Mutation 7 105177186 T C 61 78 LUAD TCGA-05-4396 RINT1 SNP Missense_Mutation 7 105195597 C A 24 81 OV TCGA-13-1404 RINT1 SNP Missense_Mutation 7 105183036 T C 52 88 LUSC TCGA-21-1076 RINT1 SNP Missense_Mutation 7 105192040 A G 4 91 LUSC TCGA-22-5472 RINT1 SNP Silent 7 105177043 T C 57 50 OV TCGA-24-1424 RINT1 SNP Missense_Mutation 7 105187424 G T 42 74 OV TCGA-24-2267 RINT1 SNP Silent 7 105187420 T G 53 47 LUSC TCGA-37-4133 RINT1 SNP Missense_Mutation 7 105204390 G C 33 84 LUAD TCGA-44-6777 RINT1 SNP Missense_Mutation 7 105190829 G T 35 73 LUSC TCGA-66-2727 RINT1 SNP Missense_Mutation 7 105204355 G T 33 64 LUSC TCGA-66-2763 RINT1 SNP Missense_Mutation 7 105207724 A T 4 76 BRCA TCGA-A1-A0SI RINT1 SNP Nonsense_Mutation 7 105205803 C T 19 50 BRCA TCGA-A8-A09A RINT1 SNP Missense_Mutation 7 105187507 A T 1 55 CRC TCGA-AA-3525 RINT1 SNP Missense_Mutation 7 105195523 A G 11 60 CRC TCGA-AA-3949 RINT1 DEL Frame_Shift_Del 7 105182902 A - 13 57 CRC TCGA-AA-3984 RINT1 SNP Nonsense_Mutation 7 105182891 C T 31 65 CRC TCGA-AG-A002 RINT1 SNP Missense_Mutation 7 105195543 G T 33 97 UCEC TCGA-AP-A051 RINT1 SNP Silent 7 105182980 C T 26 50 UCEC TCGA-AP-A051 RINT1 SNP Missense_Mutation 7 105204232 C A 20 73 UCEC TCGA-AP-A051 RINT1 SNP Silent 7 105207701 A G 2 50 UCEC TCGA-AP-A056 RINT1 SNP Missense_Mutation 7 105195486 A C 1 67 UCEC TCGA-AP-A059 RINT1 SNP Missense_Mutation 7 105183030 G T 34 48 UCEC TCGA-AP-A059 RINT1 SNP Silent 7 105190606 C T 19 55 UCEC TCGA-AP-A0LM RINT1 SNP Nonsense_Mutation 7 105187707 C T 31 65 UCEC TCGA-B5-A11E RINT1 SNP Silent 7 105195515 G A 36 58 UCEC TCGA-BG-A0VV RINT1 SNP Missense_Mutation 7 105195507 A C 1 73 HNSC TCGA-CN-4723 RINT1 SNP Missense_Mutation 7 105189098 C G 32 70 HNSC TCGA-CN-5360 RINT1 SNP Silent 7 105190713 A G 4 57 HNSC TCGA-CQ-5327 RINT1 SNP Missense_Mutation 7 105183014 C G 32 81 HNSC TCGA-CR-7368 RINT1 DEL Frame_Shift_Del 7 105190824 TGAAAGGGAGC - 63 77 HNSC TCGA-CR-7402 RINT1 DNP Missense_Mutation 7 105204333 CG TA 23 73 HNSC TCGA-CV-7245 RINT1 SNP Splice_site 7 105177012 G A 44 58 UCEC TCGA-D1-A103 RINT1 SNP Silent 7 105205787 G A 40 5 UCEC TCGA-D1-A174 RINT1 SNP Missense_Mutation 7 105183047 G A 37 82 UCEC TCGA-D1-A17Q RINT1 SNP Missense_Mutation 7 105204224 G T 33 54 BRCA TCGA-E9-A22B RINT1 SNP Missense_Mutation 7 105205897 A G 14 68 BLCA TCGA-G2-A2ES RINT1 SNP Missense_Mutation 7 105189056 T A 54 51