ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0023 ARHGEF7 SNP Missense_Mutation 13 111862263 C T 29 97 DLBCL DLBCL-MAYO_DLBCL_234 ARHGEF7 SNP Missense_Mutation 13 111885558 C T 24 80 ESO ESO-161 ARHGEF7 SNP Silent 13 111935663 C A 27 61 LUAD LUAD-B00859 ARHGEF7 SNP Silent 13 111870163 G A 35 56 LUAD LUAD-CHTN-3090415 ARHGEF7 SNP Silent 13 111768020 C A 30 49 LUAD LUAD-D01603 ARHGEF7 SNP Missense_Mutation 13 111926185 G T 33 61 MEL ME037 ARHGEF7 SNP Silent 13 111870193 C T 30 58 MEL MEL-JWCI-WGS-31 ARHGEF7 SNP Silent 13 111862241 C T 23 48 MEL MEL-JWCI-WGS-34 ARHGEF7 SNP Missense_Mutation 13 111944641 C T 31 96 MEL MEL-Ma-Mel-05 ARHGEF7 SNP Silent 13 111768015 C T 24 59 MEL MEL-Ma-Mel-65 ARHGEF7 SNP Missense_Mutation 13 111870132 T A 58 90 RHAB Rhabdoid-10-355 ARHGEF7 SNP Missense_Mutation 13 111885630 A C 16 74 LUAD TCGA-05-4396 ARHGEF7 SNP Silent 13 111862251 C A 23 83 LUAD TCGA-05-4396 ARHGEF7 SNP Silent 13 111862311 C A 31 73 LUAD TCGA-05-4396 ARHGEF7 SNP Silent 13 111919901 C A 23 51 LUAD TCGA-05-4396 ARHGEF7 SNP Missense_Mutation 13 111927996 C A 21 100 LUAD TCGA-05-5428 ARHGEF7 SNP Missense_Mutation 13 111896599 C T 32 90 GBM TCGA-06-5858 ARHGEF7 SNP Missense_Mutation 13 111870210 G A 38 85 OV TCGA-13-0723 ARHGEF7 SNP Missense_Mutation 13 111938519 T G 51 89 LUAD TCGA-17-Z026 ARHGEF7 SNP Splice_Site 13 111896544 A C 15 83 LUSC TCGA-18-5592 ARHGEF7 SNP Missense_Mutation 13 111926211 T C 52 91 OV TCGA-24-2030 ARHGEF7 SNP Missense_Mutation 13 111935537 G A 38 55 GBM TCGA-28-2514 ARHGEF7 DEL Splice_site 13 111896312 AAGT - 9 82 LUSC TCGA-37-5819 ARHGEF7 SNP Nonsense_Mutation 13 111932896 G T 45 85 LUAD TCGA-44-2668 ARHGEF7 SNP Missense_Mutation 13 111896616 G T 40 77 LUAD TCGA-44-2668 ARHGEF7 SNP Missense_Mutation 13 111929984 G C 48 66 LUSC TCGA-56-5898 ARHGEF7 SNP Missense_Mutation 13 111944527 G T 33 97 LUAD TCGA-64-5779 ARHGEF7 SNP Silent 13 111927998 G A 35 61 LUAD TCGA-67-3771 ARHGEF7 DEL Frame_Shift_Del 13 111767915 G - 47 55 BRCA TCGA-A2-A0YK ARHGEF7 SNP Nonsense_Mutation 13 111930018 C T 29 99 UCEC TCGA-A5-A0GP ARHGEF7 SNP Missense_Mutation 13 111857651 G A 45 97 CRC TCGA-A6-2670 ARHGEF7 SNP Missense_Mutation 13 111919981 A G 4 88 CRC TCGA-AA-3811 ARHGEF7 SNP Missense_Mutation 13 111896291 C T 19 76 CRC TCGA-AA-3811 ARHGEF7 SNP Missense_Mutation 13 111944540 G A 40 97 CRC TCGA-AA-3947 ARHGEF7 DEL Frame_Shift_Del 13 111767934 A - 5 83 CRC TCGA-AA-3977 ARHGEF7 SNP Silent 13 111938574 C T 31 48 CRC TCGA-AA-A00E ARHGEF7 SNP Missense_Mutation 13 111944621 A G 14 89 CRC TCGA-AA-A00R ARHGEF7 SNP Missense_Mutation 13 111953184 A T 12 56 CRC TCGA-AA-A022 ARHGEF7 SNP Missense_Mutation 13 111935663 C T 27 61 CRC TCGA-AG-3898 ARHGEF7 SNP Silent 13 111926252 C T 24 99 UCEC TCGA-AP-A056 ARHGEF7 SNP Missense_Mutation 13 111929939 G T 33 77 UCEC TCGA-AP-A056 ARHGEF7 SNP Missense_Mutation 13 111955399 A C 3 68 UCEC TCGA-AP-A059 ARHGEF7 SNP Missense_Mutation 13 111932971 G A 44 68 UCEC TCGA-AP-A059 ARHGEF7 SNP Splice_Site 13 111955337 G T 35 82 UCEC TCGA-AP-A0LM ARHGEF7 SNP Nonsense_Mutation 13 111885599 G T 35 80 UCEC TCGA-AP-A0LM ARHGEF7 SNP Missense_Mutation 13 111940763 G A 38 95 UCEC TCGA-AX-A05Z ARHGEF7 SNP Nonsense_Mutation 13 111896631 G T 33 90 UCEC TCGA-AX-A0J1 ARHGEF7 SNP Silent 13 111953840 C T 23 36 CRC TCGA-AY-4070 ARHGEF7 SNP Missense_Mutation 13 111919927 G C 46 78 KIRC TCGA-B0-5812 ARHGEF7 SNP Missense_Mutation 13 111932908 G T 36 85 UCEC TCGA-B5-A0JY ARHGEF7 SNP Missense_Mutation 13 111767943 A G 8 71 UCEC TCGA-B5-A11E ARHGEF7 SNP Missense_Mutation 13 111896229 A C 4 82 UCEC TCGA-B5-A11E ARHGEF7 SNP Missense_Mutation 13 111953860 A C 9 87 UCEC TCGA-BG-A18C ARHGEF7 SNP Silent 13 111940783 C G 29 45 BRCA TCGA-BH-A1EO ARHGEF7 SNP Missense_Mutation 13 111927898 G A 39 100 UCEC TCGA-BS-A0UJ ARHGEF7 SNP Missense_Mutation 13 111935652 T C 55 89 UCEC TCGA-BS-A0UV ARHGEF7 SNP Missense_Mutation 13 111896601 T G 64 83 BRCA TCGA-C8-A274 ARHGEF7 SNP Silent 13 111955406 G A 45 54 KIRC TCGA-CJ-4892 ARHGEF7 INS Frame_Shift_Ins 13 111944499 - T 32 79 HNSC TCGA-CN-4723 ARHGEF7 SNP Silent 13 111927983 C T 29 43 HNSC TCGA-CV-6956 ARHGEF7 SNP Silent 13 111919973 T C 52 56 HNSC TCGA-CV-7235 ARHGEF7 SNP Missense_Mutation 13 111953845 A G 16 87 HNSC TCGA-CV-7414 ARHGEF7 SNP Missense_Mutation 13 111919901 C G 23 51 KIRC TCGA-CW-5585 ARHGEF7 SNP Missense_Mutation 13 111953859 G A 45 94 UCEC TCGA-D1-A103 ARHGEF7 SNP Missense_Mutation 13 111938512 A G 13 89 UCEC TCGA-D1-A15X ARHGEF7 SNP Silent 13 111935593 G A 38 40 UCEC TCGA-D1-A176 ARHGEF7 SNP Silent 13 111870106 C A 24 45 UCEC TCGA-D1-A17D ARHGEF7 SNP Missense_Mutation 13 111932909 T C 59 90 BRCA TCGA-D8-A1JJ ARHGEF7 SNP Silent 13 111806290 C T 25 55 UCEC TCGA-DI-A0WH ARHGEF7 SNP Missense_Mutation 13 111870209 C T 27 75 BLCA TCGA-DK-A3IS ARHGEF7 SNP Splice_site 13 111929934 G A 41 99 BLCA TCGA-G2-A2EF ARHGEF7 SNP Missense_Mutation 13 111932947 G C 41 85