ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62421 APLF SNP Missense 2 68765214 G C 45 51 HNSC HN_62854 APLF SNP Missense 2 68805089 G C 33 83 LUAD LUAD-CHTN-MAD06-00668 APLF SNP Missense_Mutation 2 68753289 G T 41 51 LUAD LUAD-S01357 APLF SNP Missense_Mutation 2 68772389 G T 43 46 MEL MEL-Ma-Mel-102 APLF SNP Missense_Mutation 2 68772326 C T 30 87 LUAD TCGA-05-4396 APLF SNP Silent 2 68740266 C A 23 39 LUAD TCGA-05-4396 APLF SNP Silent 2 68740347 C A 21 50 LUAD TCGA-05-4396 APLF SNP Silent 2 68804995 C A 21 48 LUAD TCGA-05-4417 APLF DNP Nonsense_Mutation 2 68765342 TG AT 51 55 OV TCGA-09-2051 APLF SNP Missense_Mutation 2 68765169 T G 55 47 LUSC TCGA-18-3414 APLF SNP Missense_Mutation 2 68772369 A T 16 62 LUSC TCGA-21-1070 APLF SNP Missense_Mutation 2 68794484 A T 7 71 OV TCGA-25-1630 APLF SNP Silent 2 68740805 C T 29 51 GBM TCGA-28-5208 APLF SNP Missense_Mutation 2 68729870 C G 17 50 OV TCGA-36-1568 APLF SNP Missense_Mutation 2 68805019 C A 28 59 LUAD TCGA-50-5051 APLF SNP Silent 2 68772346 T C 61 54 LUSC TCGA-60-2721 APLF SNP Silent 2 68765102 T C 63 51 LUAD TCGA-91-6831 APLF SNP Missense_Mutation 2 68804987 G T 47 79 BRCA TCGA-A1-A0SE APLF SNP Silent 2 68765324 G A 33 58 BRCA TCGA-A8-A08F APLF SNP Silent 2 68740326 A T 15 57 CRC TCGA-AA-3811 APLF SNP Nonsense_Mutation 2 68717382 C T 27 54 CRC TCGA-AA-A00E APLF SNP Missense_Mutation 2 68765235 G C 45 55 CRC TCGA-AG-A002 APLF SNP Missense_Mutation 2 68717383 G A 37 79 CRC TCGA-AG-A002 APLF SNP Missense_Mutation 2 68794511 C T 19 50 CRC TCGA-AG-A015 APLF SNP Nonsense_Mutation 2 68740774 T G 61 48 BRCA TCGA-AN-A0XT APLF SNP Missense_Mutation 2 68794511 C T 19 50 UCEC TCGA-AP-A059 APLF SNP Missense_Mutation 2 68794511 C T 19 50 UCEC TCGA-B5-A0JY APLF SNP Missense_Mutation 2 68765185 C T 31 42 UCEC TCGA-B5-A11E APLF SNP Missense_Mutation 2 68765185 C T 31 42 UCEC TCGA-B5-A11E APLF SNP Missense_Mutation 2 68765266 C T 20 56 KIRC TCGA-B8-5552 APLF DEL Frame_Shift_Del 2 68805143 A - 9 78 BRCA TCGA-BH-A18J APLF SNP Missense_Mutation 2 68804999 G A 45 83 KIRC TCGA-BP-4338 APLF SNP Silent 2 68772385 C T 31 43 UCEC TCGA-BS-A0UF APLF SNP Missense_Mutation 2 68740234 G T 33 67 UCEC TCGA-BS-A0UV APLF SNP Missense_Mutation 2 68765113 C A 32 58 HNSC TCGA-CN-4726 APLF SNP Missense_Mutation 2 68740274 A G 4 57 HNSC TCGA-CN-4735 APLF SNP Missense_Mutation 2 68765290 C T 29 69 HNSC TCGA-CR-5248 APLF SNP Missense_Mutation 2 68805097 G C 33 47 HNSC TCGA-CV-5976 APLF SNP Missense_Mutation 2 68729908 C T 28 56 HNSC TCGA-CV-7253 APLF SNP Silent 2 68772424 C G 24 52 HNSC TCGA-CV-7430 APLF SNP Missense_Mutation 2 68772422 C G 30 87 KIRC TCGA-CW-5589 APLF SNP Missense_Mutation 2 68740264 C A 22 66 UCEC TCGA-D1-A16X APLF SNP Nonsense_Mutation 2 68753219 G T 33 57 BRCA TCGA-E2-A1IH APLF SNP Missense_Mutation 2 68740758 A T 12 75 BRCA TCGA-E9-A22G APLF SNP Missense_Mutation 2 68717336 A C 11 63