ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW216 EHMT2 SNP Missense_Mutation 6 31856184 C A 18 82 DLBCL DLBCL-MAYO_DLBCL_234 EHMT2 SNP Silent 6 31852532 G A 39 41 ESO ESO-114 EHMT2 SNP Missense_Mutation 6 31848572 G T 45 63 HNSC HN_63080 EHMT2 SNP Missense 6 31857264 G A 45 71 LUAD LUAD-CHTN-MAD06-00668 EHMT2 SNP Missense_Mutation 6 31856393 C T 29 82 LUAD LUAD-NYU776 EHMT2 SNP Missense_Mutation 6 31848462 C G 22 91 MEL ME009 EHMT2 SNP Silent 6 31864214 C T 22 52 MEL MEL-JWCI-WGS-15 EHMT2 SNP Silent 6 31848494 G A 37 42 MEL MEL-JWCI-WGS-7 EHMT2 SNP Missense_Mutation 6 31857067 G A 47 73 MEL MEL-Ma-Mel-114 EHMT2 SNP Silent 6 31847882 G A 43 68 MEL MEL-Ma-Mel-48 EHMT2 SNP Silent 6 31851607 G A 37 29 MEL MEL-Ma-Mel-63 EHMT2 SNP Silent 6 31852177 G A 45 62 MEL MEL-Ma-Mel-65 EHMT2 SNP Missense_Mutation 6 31855899 G A 44 71 MEL MEL-UKRV-Mel-20 EHMT2 SNP Missense_Mutation 6 31852256 G A 41 93 MM MM-0582 EHMT2 SNP Missense_Mutation 6 31847923 G A 39 78 GBM TCGA-06-5858 EHMT2 SNP Missense_Mutation 6 31852241 G A 38 94 GBM TCGA-06-6389 EHMT2 SNP Silent 6 31847948 A T 5 50 OV TCGA-13-0887 EHMT2 SNP Missense_Mutation 6 31864266 G A 41 72 LUSC TCGA-18-3406 EHMT2 SNP Nonsense_Mutation 6 31864517 G T 45 76 OV TCGA-20-0991 EHMT2 SNP Silent 6 31855630 A C 1 53 LUSC TCGA-22-5480 EHMT2 SNP Silent 6 31854777 G A 34 58 LUAD TCGA-44-6777 EHMT2 SNP Missense_Mutation 6 31857313 C G 32 83 LUAD TCGA-55-1594 EHMT2 SNP Silent 6 31855382 G A 38 52 GBM TCGA-76-6192 EHMT2 SNP Missense_Mutation 6 31856011 G A 39 91 CRC TCGA-AA-3558 EHMT2 SNP Missense_Mutation 6 31851681 C T 23 95 CRC TCGA-AG-3999 EHMT2 SNP Missense_Mutation 6 31860203 C T 27 65 CRC TCGA-AG-A02N EHMT2 SNP Missense_Mutation 6 31854575 G A 38 56 KIRC TCGA-AK-3450 EHMT2 SNP Missense_Mutation 6 31851591 G C 47 90 UCEC TCGA-AP-A056 EHMT2 SNP Missense_Mutation 6 31857249 T G 50 67 UCEC TCGA-AX-A0J1 EHMT2 SNP Missense_Mutation 6 31851623 G A 40 82 UCEC TCGA-AX-A0J1 EHMT2 SNP Silent 6 31860607 G T 35 59 KIRC TCGA-B0-5096 EHMT2 SNP Missense_Mutation 6 31855386 T C 55 76 HNSC TCGA-CR-6481 EHMT2 SNP Missense_Mutation 6 31856391 C G 32 59 HNSC TCGA-CV-6941 EHMT2 SNP Missense_Mutation 6 31855962 G A 43 92 HNSC TCGA-CV-6959 EHMT2 SNP Silent 6 31847881 G A 35 54 HNSC TCGA-CV-7102 EHMT2 SNP Missense_Mutation 6 31860266 T C 54 77 HNSC TCGA-CV-7245 EHMT2 SNP Missense_Mutation 6 31854582 C T 21 84 HNSC TCGA-CV-7254 EHMT2 SNP Splice_site 6 31864040 C T 24 87 KIRC TCGA-CZ-5459 EHMT2 SNP Missense_Mutation 6 31848507 C T 31 91 HNSC TCGA-D6-6516 EHMT2 SNP Missense_Mutation 6 31864272 G A 43 84 HNSC TCGA-DQ-5625 EHMT2 SNP Silent 6 31855970 G C 33 54 BLCA TCGA-GD-A2C5 EHMT2 SNP Missense_Mutation 6 31847893 C G 31 89 BLCA TCGA-GV-A3JX EHMT2 SNP Missense_Mutation 6 31855876 G C 41 69 HNSC TCGA-HL-7533 EHMT2 SNP Missense_Mutation 6 31856205 C G 29 95