ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0103 HPGDS SNP Missense_Mutation 4 95255725 C T 19 81 ESO ESO-721 HPGDS SNP Splice_Site_SNP 4 95264029 A G 12 49 LUAD LUAD-B01811 HPGDS SNP Missense_Mutation 4 95223334 G T 48 51 MEL MEL-13591 HPGDS SNP Missense_Mutation 4 95229885 C T 30 80 MEL MEL-JWCI-27 HPGDS SNP Missense_Mutation 4 95255717 A T 4 76 MEL MEL-Ma-Mel-65 HPGDS SNP Silent 4 95220676 A G 7 48 OV TCGA-23-1022 HPGDS DEL Frame_Shift_Del 4 95239089 A - 5 72 LUSC TCGA-39-5022 HPGDS SNP Silent 4 95220778 G A 33 84 LUAD TCGA-75-5126 HPGDS SNP Missense_Mutation 4 95239050 A T 16 72 BRCA TCGA-A2-A0YM HPGDS SNP Missense_Mutation 4 95223325 C A 22 58 UCEC TCGA-AP-A0LM HPGDS SNP Missense_Mutation 4 95220769 C A 32 50 UCEC TCGA-B5-A0JY HPGDS SNP Nonsense_Mutation 4 95229877 C A 32 80 KIRC TCGA-BP-4329 HPGDS SNP Missense_Mutation 4 95229888 G A 34 68 BLCA TCGA-BT-A0YX HPGDS SNP Splice_site 4 95223298 G A 33 58 HNSC TCGA-CR-7388 HPGDS SNP Silent 4 95223375 C T 25 50 UCEC TCGA-D1-A103 HPGDS SNP Missense_Mutation 4 95255696 A G 14 75 BRCA TCGA-E9-A1RH HPGDS SNP Missense_Mutation 4 95239059 C A 28 77