ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0037 NEIL1 SNP Missense_Mutation 15 75644477 G C 41 72 MEL ME009 NEIL1 SNP Silent 15 75641561 G A 38 20 MEL MEL-Ma-Mel-48 NEIL1 SNP Missense_Mutation 15 75647031 G A 37 43 NB NB-1110 NEIL1 SNP Missense_Mutation 15 75647341 C A 21 48 LUAD TCGA-05-4244 NEIL1 SNP Missense_Mutation 15 75641515 G T 38 54 GBM TCGA-14-1043 NEIL1 SNP Silent 15 75641495 C T 28 51 LUSC TCGA-18-3416 NEIL1 SNP Missense_Mutation 15 75644693 C T 23 68 LUSC TCGA-22-5492 NEIL1 SNP Missense_Mutation 15 75647319 C T 23 52 CRC TCGA-AA-3833 NEIL1 SNP Missense_Mutation 15 75646997 G A 38 55 CRC TCGA-AA-3864 NEIL1 SNP Missense_Mutation 15 75641646 G T 39 95 CRC TCGA-AA-A00D NEIL1 SNP Missense_Mutation 15 75644493 G A 39 58 CRC TCGA-AA-A00N NEIL1 SNP Missense_Mutation 15 75647145 G A 37 36 CRC TCGA-AA-A01R NEIL1 SNP Missense_Mutation 15 75646104 G A 34 47 AML TCGA-AB-2804 NEIL1 SNP Nonsense_Mutation 15 75647144 C T 27 45 UCEC TCGA-AX-A060 NEIL1 SNP Missense_Mutation 15 75644553 G A 39 93 BRCA TCGA-B6-A0RN NEIL1 SNP Missense_Mutation 15 75647320 G A 39 46 UCEC TCGA-BS-A0TJ NEIL1 SNP Missense_Mutation 15 75641589 G A 40 95 BLCA TCGA-BT-A3PH NEIL1 SNP Nonsense_Mutation 15 75641328 G T 41 64 BRCA TCGA-C8-A12M NEIL1 SNP Nonsense_Mutation 15 75647144 C T 27 45 BRCA TCGA-C8-A1HM NEIL1 SNP Missense_Mutation 15 75641571 C T 23 61 HNSC TCGA-CV-7247 NEIL1 SNP Missense_Mutation 15 75641409 G A 41 95 HNSC TCGA-CV-7406 NEIL1 SNP Missense_Mutation 15 75641389 C T 29 71 UCEC TCGA-D1-A174 NEIL1 SNP Missense_Mutation 15 75641440 G T 43 59 UCEC TCGA-D1-A17B NEIL1 DEL In_Frame_Del 15 75646108 GGA - 43 48 UCEC TCGA-D1-A17Q NEIL1 SNP Missense_Mutation 15 75641330 G T 33 58 BRCA TCGA-D8-A27L NEIL1 SNP Missense_Mutation 15 75641328 G A 41 64 HNSC TCGA-HD-7229 NEIL1 SNP Silent 15 75641450 C G 22 50