ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-CHTN-Z4716A KDELC2 SNP Missense_Mutation 11 108348402 C T 24 94 LUAD LUAD-D01603 KDELC2 SNP Nonsense_Mutation 11 108352913 C A 21 83 MEL MEL-13463 KDELC2 SNP Silent 11 108357061 G A 35 49 MEL MEL-JWCI-WGS-29 KDELC2 SNP Missense_Mutation 11 108345672 G A 42 80 MM MM-0605 KDELC2 SNP Nonsense_Mutation 11 108352849 C T 21 97 PRAD P04-1084 KDELC2 SNP Missense_Mutation 11 108345632 C T 21 96 LUAD TCGA-05-4396 KDELC2 SNP Silent 11 108345650 G T 39 40 LUAD TCGA-05-4432 KDELC2 SNP Missense_Mutation 11 108352829 T C 56 59 GBM TCGA-06-5414 KDELC2 SNP Missense_Mutation 11 108350192 C T 19 85 GBM TCGA-06-6697 KDELC2 SNP Missense_Mutation 11 108345675 T A 49 87 LUAD TCGA-17-Z018 KDELC2 SNP Missense_Mutation 11 108348368 T C 59 60 GBM TCGA-19-5947 KDELC2 SNP Missense_Mutation 11 108361783 C T 24 74 OV TCGA-23-2077 KDELC2 SNP Silent 11 108350193 G A 39 21 GBM TCGA-32-1979 KDELC2 SNP Missense_Mutation 11 108352840 G C 33 97 LUSC TCGA-39-5022 KDELC2 SNP Missense_Mutation 11 108348418 C G 32 63 LUSC TCGA-39-5035 KDELC2 SNP Missense_Mutation 11 108357165 G A 44 96 CRC TCGA-AA-3949 KDELC2 SNP Silent 11 108350130 C T 27 31 CRC TCGA-AA-A022 KDELC2 SNP Missense_Mutation 11 108348342 C T 20 72 CRC TCGA-AG-A02N KDELC2 SNP Missense_Mutation 11 108361840 C T 23 68 UCEC TCGA-AX-A05Z KDELC2 SNP Missense_Mutation 11 108361799 A G 4 75 HNSC TCGA-BA-5151 KDELC2 SNP Silent 11 108350193 G T 39 21 UCEC TCGA-BS-A0UF KDELC2 SNP Missense_Mutation 11 108350068 C A 32 99 BLCA TCGA-BT-A3PJ KDELC2 SNP Missense_Mutation 11 108357021 G A 43 96 HNSC TCGA-CR-7389 KDELC2 SNP Silent 11 108348424 T C 56 65 UCEC TCGA-D1-A167 KDELC2 SNP Missense_Mutation 11 108361813 C A 24 96 BLCA TCGA-DK-A3IM KDELC2 SNP Missense_Mutation 11 108357060 A G 3 88 BRCA TCGA-E9-A1R5 KDELC2 SNP Missense_Mutation 11 108361856 G T 44 55