ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-CHTN-Z4716A SERGEF SNP Missense_Mutation 11 17981140 C A 28 50 LUAD LUAD-NYU1051S SERGEF SNP Nonsense_Mutation 11 17809916 C A 23 93 LUAD LUAD-S01346 SERGEF SNP Missense_Mutation 11 18029584 C T 30 80 MEL MEL-JWCI-WGS-38 SERGEF SNP Silent 11 18010238 G A 41 56 MEL MEL-Ma-Mel-65 SERGEF SNP Silent 11 17981080 G A 41 55 MEL MEL-Ma-Mel-85 SERGEF SNP Missense_Mutation 11 17809931 C T 29 93 MM MM-0473 SERGEF SNP Missense_Mutation 11 17809888 G A 42 64 LUAD TCGA-05-4396 SERGEF SNP Missense_Mutation 11 17809643 C A 21 52 LUAD TCGA-05-4396 SERGEF SNP Missense_Mutation 11 17809670 G T 47 65 LUSC TCGA-33-6737 SERGEF SNP Silent 11 18029510 C T 22 32 LUSC TCGA-46-3767 SERGEF SNP Splice_site 11 18014479 T G 55 57 LUAD TCGA-50-5066 SERGEF SNP Silent 11 18028280 G A 33 55 CRC TCGA-A6-2678 SERGEF SNP Missense_Mutation 11 17809888 G T 42 64 CRC TCGA-AA-3516 SERGEF SNP Silent 11 18029507 G C 42 53 CRC TCGA-AA-3518 SERGEF SNP Missense_Mutation 11 18028188 C T 17 77 CRC TCGA-AA-3672 SERGEF SNP Missense_Mutation 11 18017391 G T 46 51 AML TCGA-AB-2863 SERGEF SNP Missense_Mutation 11 17981114 T C 62 64 CRC TCGA-AG-A002 SERGEF SNP Splice_site 11 18014478 C A 24 79 UCEC TCGA-AP-A056 SERGEF SNP Missense_Mutation 11 17809945 G T 33 93 UCEC TCGA-AP-A056 SERGEF SNP Missense_Mutation 11 17981098 T G 64 45 UCEC TCGA-AP-A056 SERGEF SNP Silent 11 18010268 C T 28 51 UCEC TCGA-AP-A056 SERGEF SNP Splice_site 11 18017455 C T 31 44 UCEC TCGA-B5-A11N SERGEF SNP Missense_Mutation 11 17899774 C T 28 53 HNSC TCGA-BA-6869 SERGEF SNP Silent 11 18010157 C G 21 52 UCEC TCGA-BS-A0UV SERGEF SNP Splice_site 11 18017455 C T 31 44 HNSC TCGA-CN-5359 SERGEF SNP Missense_Mutation 11 17981067 G A 44 56 HNSC TCGA-CR-7401 SERGEF SNP Missense_Mutation 11 18028145 C A 25 41 UCEC TCGA-D1-A103 SERGEF SNP Missense_Mutation 11 18017406 G A 40 69