ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0059 OR5H1 SNP Silent 3 97852252 C A 24 52 ESO ESO-1059 OR5H1 SNP Missense_Mutation 3 97852339 A C 3 42 ESO ESO-130 OR5H1 SNP Missense_Mutation 3 97851876 G A 48 58 LUAD LUAD-CHTN-Z4716A OR5H1 SNP Missense_Mutation 3 97852067 C A 29 59 MEL ME002 OR5H1 SNP Silent 3 97852468 T C 61 47 MEL ME010 OR5H1 SNP Silent 3 97852405 C T 29 43 MEL MEL-13600 OR5H1 SNP Missense_Mutation 3 97852023 G A 41 46 MEL MEL-JWCI-WGS-7 OR5H1 SNP Missense_Mutation 3 97851588 G A 41 62 MEL MEL-JWCI-WGS-7 OR5H1 SNP Missense_Mutation 3 97852388 C T 30 86 MEL MEL-Ma-Mel-48 OR5H1 SNP Missense_Mutation 3 97852023 G A 41 46 LUAD TCGA-05-4417 OR5H1 SNP Missense_Mutation 3 97852389 C A 24 68 GBM TCGA-12-1597 OR5H1 SNP Missense_Mutation 3 97852262 T A 55 82 LUAD TCGA-17-Z003 OR5H1 SNP Nonsense_Mutation 3 97852218 T A 61 55 LUAD TCGA-17-Z030 OR5H1 SNP Nonsense_Mutation 3 97852075 C A 20 50 LUAD TCGA-17-Z051 OR5H1 SNP Silent 3 97851823 C A 32 50 GBM TCGA-19-2631 OR5H1 SNP Missense_Mutation 3 97851558 C G 25 40 LUSC TCGA-21-1076 OR5H1 SNP Missense_Mutation 3 97851588 G T 41 62 OV TCGA-24-1422 OR5H1 SNP Missense_Mutation 3 97852398 A T 4 81 GBM TCGA-26-6174 OR5H1 SNP Silent 3 97852369 A G 16 43 GBM TCGA-27-1837 OR5H1 SNP Silent 3 97851850 G A 40 42 LUSC TCGA-34-2600 OR5H1 SNP Nonsense_Mutation 3 97852476 C G 29 58 LUAD TCGA-38-4631 OR5H1 INS Frame_Shift_Ins 3 97852271 - A 21 88 LUSC TCGA-43-6143 OR5H1 SNP Splice_site 3 97851543 T C 51 55 LUSC TCGA-43-6143 OR5H1 SNP Missense_Mutation 3 97852069 C G 17 51 LUSC TCGA-43-6647 OR5H1 SNP Missense_Mutation 3 97852280 T A 54 56 LUAD TCGA-49-6743 OR5H1 SNP Missense_Mutation 3 97852089 C A 21 75 LUAD TCGA-64-1676 OR5H1 SNP Missense_Mutation 3 97851886 G T 47 53 LUSC TCGA-66-2755 OR5H1 SNP Missense_Mutation 3 97852251 C A 26 68 LUSC TCGA-66-2755 OR5H1 SNP Silent 3 97852252 C A 24 52 GBM TCGA-76-6191 OR5H1 SNP Silent 3 97852415 C T 32 50 LUAD TCGA-91-6829 OR5H1 SNP Silent 3 97852015 C A 30 40 BRCA TCGA-A2-A25D OR5H1 SNP Missense_Mutation 3 97852403 A G 16 44 BRCA TCGA-A8-A06Z OR5H1 SNP Silent 3 97851850 G A 40 42 BRCA TCGA-A8-A08L OR5H1 SNP Missense_Mutation 3 97851818 T C 50 62 CRC TCGA-AA-3949 OR5H1 SNP Missense_Mutation 3 97852131 T G 53 70 CRC TCGA-AA-3984 OR5H1 SNP Missense_Mutation 3 97852225 G T 33 48 CRC TCGA-AA-A01Q OR5H1 INS Frame_Shift_Ins 3 97852455 - A 61 57 BRCA TCGA-AN-A0FJ OR5H1 SNP Missense_Mutation 3 97851825 C G 32 54 UCEC TCGA-AP-A056 OR5H1 SNP Missense_Mutation 3 97852205 C A 32 51 UCEC TCGA-AP-A059 OR5H1 SNP Missense_Mutation 3 97851644 T C 49 78 UCEC TCGA-AX-A05W OR5H1 SNP Splice_site 3 97851540 A G 10 56 KIRC TCGA-B2-4099 OR5H1 INS Frame_Shift_Ins 3 97852455 - A 61 57 HNSC TCGA-BA-6870 OR5H1 SNP Missense_Mutation 3 97852161 A G 7 52 BRCA TCGA-BH-A0HI OR5H1 SNP Silent 3 97851563 T C 52 46 UCEC TCGA-BS-A0UF OR5H1 SNP Missense_Mutation 3 97852124 A C 13 65 UCEC TCGA-BS-A0UF OR5H1 SNP Missense_Mutation 3 97852289 T G 64 50 HNSC TCGA-CR-7388 OR5H1 SNP Missense_Mutation 3 97852332 C G 32 75 HNSC TCGA-CR-7388 OR5H1 SNP Missense_Mutation 3 97852367 C G 32 50 HNSC TCGA-CV-5442 OR5H1 DEL In_Frame_Del 3 97851704 CTT - 24 64 HNSC TCGA-CV-6935 OR5H1 SNP Missense_Mutation 3 97852283 G T 48 59 BLCA TCGA-DK-A3IT OR5H1 SNP Missense_Mutation 3 97852160 C G 29 57 BRCA TCGA-EW-A1PE OR5H1 SNP Silent 3 97851916 C T 21 50 HNSC TCGA-HL-7533 OR5H1 SNP Missense_Mutation 3 97852279 C G 32 9