ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B00523 OXER1 SNP Missense_Mutation 2 42990325 A G 11 60 LUAD LUAD-B00523 OXER1 SNP Missense_Mutation 2 42990327 G T 44 51 LUAD LUAD-F00368 OXER1 SNP Missense_Mutation 2 42990502 A T 6 51 MEL MEL-JWCI-WGS-1 OXER1 SNP Missense_Mutation 2 42990337 C T 31 26 MEL MEL-JWCI-WGS-25 OXER1 SNP Missense_Mutation 2 42990265 G A 43 78 LUAD TCGA-35-3621 OXER1 SNP Missense_Mutation 2 42991141 G C 41 59 LUAD TCGA-44-3398 OXER1 SNP Missense_Mutation 2 42990262 A T 6 55 LUAD TCGA-91-6836 OXER1 SNP Silent 2 42990264 G T 39 21 CRC TCGA-A6-2676 OXER1 SNP Missense_Mutation 2 42990878 G A 39 62 CRC TCGA-AA-3672 OXER1 SNP Missense_Mutation 2 42990277 C T 20 70 UCEC TCGA-AP-A0LM OXER1 SNP Missense_Mutation 2 42990328 T G 58 56 HNSC TCGA-BA-4075 OXER1 SNP Silent 2 42991086 G A 35 44 KIRC TCGA-BP-4756 OXER1 SNP Missense_Mutation 2 42991163 A G 11 53 HNSC TCGA-CV-6959 OXER1 SNP Missense_Mutation 2 42991037 G C 35 60 UCEC TCGA-D1-A15X OXER1 SNP Silent 2 42990177 G A 38 41 BRCA TCGA-E2-A14P OXER1 SNP Missense_Mutation 2 42990664 C T 26 50 BRCA TCGA-E9-A1NC OXER1 INS Frame_Shift_Ins 2 42990217 - C 42 65 BRCA TCGA-EW-A1J5 OXER1 SNP Missense_Mutation 2 42990854 C G 29 53 CARC Carc-BWH17 OXER1 SNP Missense_Mutation 2 42990225 C G 32 67