ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW161 LIN7A SNP Missense_Mutation 12 81283088 T A 59 91 ESO ESO-0149 LIN7A SNP Missense_Mutation 12 81205350 C T 27 86 ESO ESO-327 LIN7A SNP Nonsense_Mutation 12 81242083 C A 29 98 LUAD LUAD-E00897 LIN7A SNP Missense_Mutation 12 81331470 G A 40 77 LUAD LUAD-YINHD LIN7A SNP Missense_Mutation 12 81283087 G T 48 55 MED MD-279 LIN7A SNP Missense_Mutation 12 81205324 G A 38 85 MEL ME050 LIN7A SNP Nonsense_Mutation 12 81331441 G A 47 79 MEL MEL-JWCI-WGS-1 LIN7A SNP Missense_Mutation 12 81239618 C T 30 100 MEL MEL-Ma-Mel-102 LIN7A SNP Missense_Mutation 12 81239623 C T 21 87 LUAD TCGA-17-Z046 LIN7A SNP Missense_Mutation 12 81283099 T G 56 51 LUSC TCGA-21-1076 LIN7A SNP Missense_Mutation 12 81205404 C A 28 69 LUAD TCGA-44-6776 LIN7A SNP Missense_Mutation 12 81239642 C A 26 100 OV TCGA-59-2352 LIN7A SNP Missense_Mutation 12 81205398 T C 56 91 LUSC TCGA-66-2759 LIN7A SNP Silent 12 81205391 C A 21 60 CRC TCGA-AA-3555 LIN7A SNP Silent 12 81242046 G A 38 98 CRC TCGA-AA-A00Q LIN7A SNP Missense_Mutation 12 81205435 C T 28 99 UCEC TCGA-AP-A051 LIN7A SNP Missense_Mutation 12 81205324 G A 38 85 UCEC TCGA-AP-A051 LIN7A SNP Silent 12 81205382 G A 48 71 UCEC TCGA-AP-A056 LIN7A SNP Missense_Mutation 12 81239672 C T 31 100 KIRC TCGA-B0-4844 LIN7A SNP Silent 12 81239680 G C 43 51 KIRC TCGA-B0-5094 LIN7A SNP Silent 12 81239638 A T 5 51 UCEC TCGA-B5-A0JY LIN7A SNP Missense_Mutation 12 81283065 C A 20 100 UCEC TCGA-B5-A0K6 LIN7A SNP Missense_Mutation 12 81205384 A G 16 91 UCEC TCGA-B5-A11E LIN7A SNP Silent 12 81239622 C T 22 100 HNSC TCGA-BA-6868 LIN7A SNP Splice_site 12 81331420 C A 24 66 HNSC TCGA-BB-7871 LIN7A SNP Missense_Mutation 12 81205380 G A 44 99 UCEC TCGA-BG-A18B LIN7A SNP Missense_Mutation 12 81283079 T C 63 91 UCEC TCGA-BS-A0UV LIN7A SNP Missense_Mutation 12 81239614 C A 24 54 HNSC TCGA-CV-7440 LIN7A SNP Silent 12 81331469 C A 23 50 UCEC TCGA-D1-A103 LIN7A SNP Silent 12 81242057 G A 39 20 UCEC TCGA-D1-A17Q LIN7A SNP Nonsense_Mutation 12 81205450 C A 32 99 HNSC TCGA-DQ-7588 LIN7A SNP Silent 12 81331433 G C 45 57 HNSC TCGA-F7-7848 LIN7A SNP Missense_Mutation 12 81283142 G C 46 86 CARC Carc-Asa6 LIN7A SNP Missense_Mutation 12 81242052 A C 9 75