ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_0-046 SESN2 SNP Missense 1 28598817 C A 32 83 LUAD LUAD-NYU669 SESN2 SNP Missense_Mutation 1 28607279 A T 14 85 LUAD LUAD-RT-S01702 SESN2 SNP Silent 1 28607280 C T 19 48 LUAD LUAD-RT-S01769 SESN2 SNP Missense_Mutation 1 28601484 G A 38 94 MEL MEL-JWCI-WGS-12 SESN2 SNP Missense_Mutation 1 28598342 G A 44 96 OV TCGA-04-1347 SESN2 SNP Silent 1 28601440 C T 17 62 LUAD TCGA-05-4396 SESN2 SNP Missense_Mutation 1 28598804 C A 23 53 LUAD TCGA-17-Z021 SESN2 SNP Silent 1 28599220 A T 7 44 OV TCGA-23-1024 SESN2 SNP Silent 1 28599184 C T 31 44 LUSC TCGA-34-5239 SESN2 SNP Missense_Mutation 1 28599167 C T 21 96 LUAD TCGA-35-4122 SESN2 SNP Missense_Mutation 1 28598891 C T 23 56 LUSC TCGA-43-6771 SESN2 SNP Missense_Mutation 1 28601391 G T 44 76 LUSC TCGA-43-6771 SESN2 SNP Missense_Mutation 1 28601393 G T 47 94 CRC TCGA-A6-2683 SESN2 SNP Silent 1 28599955 C T 22 57 BRCA TCGA-A8-A09G SESN2 SNP Missense_Mutation 1 28601371 C G 30 60 CRC TCGA-AA-3672 SESN2 SNP Missense_Mutation 1 28598305 T C 56 75 CRC TCGA-AA-A00E SESN2 SNP Missense_Mutation 1 28595715 C T 31 65 CRC TCGA-AA-A022 SESN2 SNP Missense_Mutation 1 28607257 C T 27 92 AML TCGA-AB-2826 SESN2 SNP Missense_Mutation 1 28598942 C T 25 96 CRC TCGA-AG-A02N SESN2 SNP Missense_Mutation 1 28605651 C T 27 70 BRCA TCGA-AO-A0JE SESN2 SNP Silent 1 28599955 C A 22 57 BRCA TCGA-AO-A12F SESN2 SNP Nonsense_Mutation 1 28598251 C T 27 69 UCEC TCGA-AP-A051 SESN2 SNP Missense_Mutation 1 28599128 G A 42 96 UCEC TCGA-AP-A0LM SESN2 SNP Missense_Mutation 1 28598805 G A 38 96 UCEC TCGA-B5-A0JR SESN2 SNP Missense_Mutation 1 28599128 G A 42 96 UCEC TCGA-BS-A0UV SESN2 SNP Silent 1 28599955 C T 22 57 UCEC TCGA-D1-A163 SESN2 SNP Silent 1 28607232 C T 19 54 HNSC TCGA-HL-7533 SESN2 SNP Silent 1 28599970 G A 33 52