ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-CHTN-3090416 CRHBP SNP Missense_Mutation 5 76264649 C A 23 55 LUAD LUAD-CHTN-MAD06-00668 CRHBP SNP Missense_Mutation 5 76249017 A G 3 50 MEL ME009 CRHBP SNP Silent 5 76251681 C T 18 58 MEL MEL-13549 CRHBP SNP Missense_Mutation 5 76249510 C G 23 73 MEL MEL-JWCI-14 CRHBP DNP Missense_Mutation 5 76259270 CC TT 22 65 MEL MEL-JWCI-WGS-1 CRHBP SNP Splice_site 5 76251688 C T 31 94 MEL MEL-JWCI-WGS-22 CRHBP SNP Silent 5 76259272 C T 24 49 MEL MEL-JWCI-WGS-6 CRHBP SNP Missense_Mutation 5 76251529 C T 29 94 MEL MEL-JWCI-WGS-7 CRHBP SNP Missense_Mutation 5 76264618 C T 31 97 MM MM-0387 CRHBP SNP Splice_Site_SNP 5 76251690 T C 57 86 LUAD TCGA-05-4382 CRHBP SNP Missense_Mutation 5 76259265 G T 46 97 LUAD TCGA-05-4430 CRHBP SNP Missense_Mutation 5 76249973 C A 21 59 LUAD TCGA-17-Z001 CRHBP SNP Missense_Mutation 5 76251567 T G 59 55 LUAD TCGA-17-Z016 CRHBP SNP Silent 5 76259266 C T 28 58 LUSC TCGA-18-3409 CRHBP SNP Missense_Mutation 5 76264654 G A 37 82 LUSC TCGA-22-4599 CRHBP SNP Silent 5 76249897 C T 23 50 KIRC TCGA-A3-3370 CRHBP SNP Missense_Mutation 5 76249908 C T 23 92 UCEC TCGA-A5-A0VP CRHBP SNP Silent 5 76264611 C T 19 52 CRC TCGA-AA-3555 CRHBP SNP Missense_Mutation 5 76259198 G A 33 97 CRC TCGA-AA-A00U CRHBP SNP Missense_Mutation 5 76254586 A G 10 60 UCEC TCGA-AP-A056 CRHBP SNP Missense_Mutation 5 76259270 C T 22 65 UCEC TCGA-AP-A059 CRHBP SNP Silent 5 76251570 G A 33 53 UCEC TCGA-AP-A0LM CRHBP SNP Silent 5 76248965 G A 38 38 UCEC TCGA-B5-A11E CRHBP SNP Missense_Mutation 5 76249029 C T 23 52 UCEC TCGA-BS-A0UL CRHBP INS In_Frame_Ins 5 76249960 - TGG 21 51 UCEC TCGA-BS-A0UV CRHBP SNP Silent 5 76249999 C T 27 48 UCEC TCGA-BS-A0UV CRHBP SNP Nonsense_Mutation 5 76264672 G T 47 76 HNSC TCGA-CV-6934 CRHBP SNP Missense_Mutation 5 76251503 G A 43 94 UCEC TCGA-D1-A103 CRHBP SNP Missense_Mutation 5 76264594 G A 44 97 HNSC TCGA-D6-6516 CRHBP SNP Missense_Mutation 5 76264687 G A 41 75