ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62415 XKR9 SNP Missense 8 71646233 A C 16 52 MEL ME044 XKR9 SNP Silent 8 71619375 G A 37 42 MEL MEL-JWCI-WGS-1 XKR9 SNP Missense_Mutation 8 71646181 C T 31 87 MEL MEL-JWCI-WGS-12 XKR9 SNP Silent 8 71646647 C T 30 53 MEL MEL-JWCI-WGS-22 XKR9 SNP Silent 8 71619234 C T 31 48 MEL MEL-JWCI-WGS-39 XKR9 SNP Silent 8 71646131 A T 12 52 MEL MEL-Ma-Mel-36 XKR9 SNP Missense_Mutation 8 71593393 C T 21 49 MEL MEL-Ma-Mel-37 XKR9 SNP Missense_Mutation 8 71646567 C T 29 88 MEL MEL-Ma-Mel-54a XKR9 SNP Silent 8 71646647 C T 30 53 PRAD P06-4428 XKR9 SNP Missense_Mutation 8 71646226 T A 52 51 GBM TCGA-06-5417 XKR9 SNP Missense_Mutation 8 71593354 G T 45 79 GBM TCGA-12-3649 XKR9 SNP Missense_Mutation 8 71646034 C T 27 52 LUSC TCGA-18-3409 XKR9 SNP Missense_Mutation 8 71646348 C T 32 67 OV TCGA-23-1124 XKR9 SNP Silent 8 71646497 T C 53 55 LUSC TCGA-51-4080 XKR9 SNP Missense_Mutation 8 71646376 G T 41 88 LUSC TCGA-66-2756 XKR9 SNP Missense_Mutation 8 71646107 G C 46 46 LUAD TCGA-91-6829 XKR9 SNP Missense_Mutation 8 71646054 T A 55 56 UCEC TCGA-A5-A0GH XKR9 SNP Translation_Start_Site 8 71593217 A G 14 53 CRC TCGA-AA-3811 XKR9 SNP Missense_Mutation 8 71646303 T A 63 68 CRC TCGA-AA-A00N XKR9 SNP Silent 8 71646500 C A 29 47 CRC TCGA-AA-A010 XKR9 SNP Missense_Mutation 8 71646380 G T 33 54 CRC TCGA-AG-A002 XKR9 SNP Silent 8 71593401 A G 10 58 CRC TCGA-AG-A002 XKR9 SNP Missense_Mutation 8 71646602 A C 1 69 UCEC TCGA-AP-A051 XKR9 SNP Missense_Mutation 8 71619290 G T 34 68 UCEC TCGA-AP-A059 XKR9 SNP Missense_Mutation 8 71646414 G A 48 57 UCEC TCGA-AP-A059 XKR9 SNP Missense_Mutation 8 71646502 G T 36 41 UCEC TCGA-AP-A0LM XKR9 SNP Missense_Mutation 8 71593311 G T 33 46 UCEC TCGA-B5-A0JY XKR9 SNP Silent 8 71593384 A C 7 62 UCEC TCGA-B5-A11E XKR9 SNP Silent 8 71646035 G A 39 46 UCEC TCGA-B5-A11E XKR9 SNP Missense_Mutation 8 71646186 A G 12 81 BRCA TCGA-B6-A0IQ XKR9 SNP Missense_Mutation 8 71593433 T G 64 64 HNSC TCGA-CV-5439 XKR9 SNP Silent 8 71619348 C G 32 51 HNSC TCGA-CV-5441 XKR9 SNP Missense_Mutation 8 71646336 G T 48 88 UCEC TCGA-D1-A103 XKR9 SNP Nonsense_Mutation 8 71593552 G T 35 79 UCEC TCGA-D1-A17Q XKR9 SNP Missense_Mutation 8 71646532 G T 41 88