ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62237 MTA2 SNP Synonymous 11 62365551 G A 38 49 HNSC HN_62426 MTA2 SNP Synonymous 11 62365141 G A 33 53 HNSC HN_62426 MTA2 SNP Missense 11 62365565 G A 33 54 HNSC HN_62624 MTA2 SNP Missense 11 62362810 C A 24 76 LUAD LUAD-D02085 MTA2 SNP Missense_Mutation 11 62362844 T C 59 88 MEL MEL-13591 MTA2 SNP Missense_Mutation 11 62365178 G A 33 70 MEL MEL-JWCI-WGS-25 MTA2 SNP Silent 11 62364160 C T 24 64 MEL MEL-Ma-Mel-114 MTA2 SNP Splice_Site 11 62365185 C T 24 90 MEL MEL-Ma-Mel-120 MTA2 SNP Missense_Mutation 11 62361795 G C 38 60 NB NB-1956 MTA2 SNP Missense_Mutation 11 62362002 G A 40 74 LUAD TCGA-05-4396 MTA2 SNP Missense_Mutation 11 62365169 C A 23 94 LUAD TCGA-05-4396 MTA2 SNP Splice_site 11 62365994 C A 23 97 LUAD TCGA-05-4396 MTA2 SNP Missense_Mutation 11 62366045 C A 23 98 LUSC TCGA-18-3421 MTA2 SNP Silent 11 62361826 C G 30 62 OV TCGA-25-2400 MTA2 SNP Missense_Mutation 11 62365832 C A 32 56 LUAD TCGA-73-4658 MTA2 SNP Missense_Mutation 11 62363320 C G 25 98 GBM TCGA-76-4925 MTA2 SNP Missense_Mutation 11 62364206 C T 23 96 CRC TCGA-A6-2672 MTA2 SNP Missense_Mutation 11 62361508 G T 35 53 CRC TCGA-AA-3977 MTA2 SNP Missense_Mutation 11 62362459 C A 32 94 CRC TCGA-AA-3977 MTA2 SNP Missense_Mutation 11 62367706 T G 56 80 CRC TCGA-AA-A01D MTA2 SNP Nonsense_Mutation 11 62363336 C T 21 96 AML TCGA-AB-2808 MTA2 SNP Splice_Site 11 62365186 T A 55 83 AML TCGA-AB-2863 MTA2 SNP Missense_Mutation 11 62364143 T C 49 89 AML TCGA-AB-2922 MTA2 SNP Missense_Mutation 11 62364125 T C 50 89 UCEC TCGA-AP-A051 MTA2 SNP Missense_Mutation 11 62362756 G A 42 73 UCEC TCGA-AP-A051 MTA2 SNP Missense_Mutation 11 62364291 C T 27 96 UCEC TCGA-AP-A059 MTA2 SNP Missense_Mutation 11 62363977 C A 20 84 CRC TCGA-AY-4071 MTA2 SNP Missense_Mutation 11 62365507 C T 27 63 KIRC TCGA-B0-4712 MTA2 SNP Missense_Mutation 11 62362921 C T 20 95 UCEC TCGA-B5-A0JR MTA2 SNP Silent 11 62366046 G T 39 64 UCEC TCGA-B5-A11E MTA2 SNP Missense_Mutation 11 62361360 A T 10 86 UCEC TCGA-B5-A11E MTA2 SNP Missense_Mutation 11 62362898 C T 27 81 UCEC TCGA-B5-A11R MTA2 SNP Silent 11 62361790 C T 32 73 UCEC TCGA-B5-A11Y MTA2 SNP Missense_Mutation 11 62362777 C T 23 74 BRCA TCGA-BH-A0HK MTA2 SNP Missense_Mutation 11 62363528 C T 29 68 KIRC TCGA-BP-4762 MTA2 SNP Missense_Mutation 11 62361740 T A 56 74 KIRC TCGA-BP-4995 MTA2 SNP Silent 11 62366080 C G 22 48 HNSC TCGA-CN-4723 MTA2 SNP Nonsense_Mutation 11 62364201 C A 29 96 HNSC TCGA-CN-4730 MTA2 SNP Missense_Mutation 11 62361854 G C 33 80 HNSC TCGA-CN-4730 MTA2 SNP Missense_Mutation 11 62362037 G A 41 70 HNSC TCGA-CR-5247 MTA2 SNP Missense_Mutation 11 62362870 T C 60 56 HNSC TCGA-CR-6472 MTA2 SNP Nonsense_Mutation 11 62365499 C A 32 84 HNSC TCGA-CR-6472 MTA2 SNP Missense_Mutation 11 62365820 C G 29 63 HNSC TCGA-CV-7423 MTA2 SNP Missense_Mutation 11 62361790 C G 32 73 BLCA TCGA-H4-A2HQ MTA2 SNP Missense_Mutation 11 62364201 C T 29 96