ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0067 LY6G6F SNP Missense_Mutation 6 31678191 C A 32 59 HNSC HN_62860 LY6G6F SNP Synonymous 6 31683367 G A 34 46 LUAD LUAD-NYU776 LY6G6F SNP Missense_Mutation 6 31675713 C T 22 65 LUAD LUAD-S01467 LY6G6F SNP Missense_Mutation 6 31675428 G T 42 59 LUAD LUAD-TJW61 LY6G6F SNP Missense_Mutation 6 31685462 G C 41 51 MEL MEL-JWCI-WGS-1 LY6G6F SNP Missense_Mutation 6 31674721 C A 20 35 MEL MEL-JWCI-WGS-11 LY6G6F SNP Missense_Mutation 6 31675345 G T 34 48 MEL MEL-JWCI-WGS-33 LY6G6F SNP Missense_Mutation 6 31675348 G A 35 53 MEL MEL-JWCI-WGS-35 LY6G6F SNP Missense_Mutation 6 31675312 G A 41 75 MEL MEL-Ma-Mel-94 LY6G6F DNP Missense_Mutation 6 31678361 CC TT 22 54 LUSC TCGA-18-3409 LY6G6F SNP Missense_Mutation 6 31675746 G A 41 77 LUSC TCGA-18-4086 LY6G6F SNP Missense_Mutation 6 31675844 G C 41 45 LUAD TCGA-35-3621 LY6G6F SNP Missense_Mutation 6 31678183 T G 63 62 LUAD TCGA-91-6836 LY6G6F SNP Missense_Mutation 6 31685371 G C 45 59 CRC TCGA-AA-A010 LY6G6F SNP Missense_Mutation 6 31677952 G T 35 47 UCEC TCGA-AP-A0LD LY6G6F SNP Missense_Mutation 6 31675860 A T 4 52 UCEC TCGA-BS-A0UF LY6G6F SNP Silent 6 31675500 C T 27 41 KIRC TCGA-CZ-4866 LY6G6F INS Frame_Shift_Ins 6 31675443 - A 41 54 BLCA TCGA-G2-A2EJ LY6G6F SNP Missense_Mutation 6 31685471 C G 24 43