ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62756 NEIL2 SNP Synonymous 8 11643686 G A 40 29 MEL MEL-JWCI-WGS-12 NEIL2 SNP Missense_Mutation 8 11637258 C T 18 43 LUAD TCGA-05-4396 NEIL2 SNP Silent 8 11643527 C A 31 21 GBM TCGA-06-0174 NEIL2 SNP Missense_Mutation 8 11643604 G A 42 38 LUSC TCGA-43-3920 NEIL2 SNP Missense_Mutation 8 11640745 G T 47 56 LUSC TCGA-66-2754 NEIL2 SNP Nonsense_Mutation 8 11637323 G T 41 43 CRC TCGA-AA-3858 NEIL2 SNP Missense_Mutation 8 11637221 G T 41 50 CRC TCGA-AA-3966 NEIL2 SNP Missense_Mutation 8 11629094 G T 35 74 CRC TCGA-AA-A00J NEIL2 SNP Silent 8 11643755 G A 35 46 CRC TCGA-AA-A02W NEIL2 DEL Frame_Shift_Del 8 11643500 C - 17 64 UCEC TCGA-AP-A059 NEIL2 SNP Silent 8 11643479 C T 29 63 UCEC TCGA-AP-A0LM NEIL2 SNP Silent 8 11637331 C T 19 44 UCEC TCGA-AX-A06H NEIL2 SNP Missense_Mutation 8 11628987 C T 29 74 UCEC TCGA-AX-A0J0 NEIL2 SNP Missense_Mutation 8 11637401 G A 37 69 HNSC TCGA-BA-4077 NEIL2 SNP Missense_Mutation 8 11643525 C G 32 70 HNSC TCGA-CV-6953 NEIL2 SNP Missense_Mutation 8 11637389 G A 40 30 HNSC TCGA-CV-7099 NEIL2 SNP Missense_Mutation 8 11637314 G C 45 36