ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-174 MAP7D2 SNP Missense_Mutation 23 20073864 C T 31 75 ESO ESO-874 MAP7D2 SNP Missense_Mutation 23 20043996 C T 27 60 HNSC HN_62755 MAP7D2 SNP Missense 23 20030560 T G 56 80 LUAD LUAD-B02216 MAP7D2 SNP Missense_Mutation 23 20030606 C A 27 40 LUAD LUAD-E01217 MAP7D2 SNP Silent 23 20029035 G A 43 49 LUAD LUAD-NYU408 MAP7D2 SNP Missense_Mutation 23 20033399 C A 19 72 MEL ME017 MAP7D2 SNP Silent 23 20043926 C T 22 49 MEL ME037 MAP7D2 DNP Missense_Mutation 23 20028977 GG AA 35 61 MEL MEL-JWCI-WGS-18 MAP7D2 SNP Splice_Site 23 20060748 C T 24 78 MEL MEL-JWCI-WGS-32 MAP7D2 SNP Missense_Mutation 23 20031739 A C 16 86 MEL MEL-JWCI-WGS-6 MAP7D2 SNP Missense_Mutation 23 20033442 C T 32 94 MEL MEL-Ma-Mel-65 MAP7D2 SNP Silent 23 20043959 C T 30 78 MEL MEL-Ma-Mel-67 MAP7D2 SNP Missense_Mutation 23 20034397 G A 37 57 NB NB-1266 MAP7D2 SNP Missense_Mutation 23 20043968 C A 25 39 LUAD TCGA-05-4382 MAP7D2 SNP Nonsense_Mutation 23 20062499 C A 24 59 LUAD TCGA-05-4396 MAP7D2 SNP Missense_Mutation 23 20029069 C A 31 61 LUAD TCGA-05-4396 MAP7D2 SNP Silent 23 20031233 C A 21 43 LUAD TCGA-05-4396 MAP7D2 SNP Missense_Mutation 23 20043894 G T 39 46 LUAD TCGA-05-4396 MAP7D2 SNP Missense_Mutation 23 20060690 C A 23 60 OV TCGA-13-0885 MAP7D2 SNP Missense_Mutation 23 20028956 G A 41 93 OV TCGA-13-0889 MAP7D2 SNP Missense_Mutation 23 20043112 C T 30 91 LUAD TCGA-17-Z056 MAP7D2 SNP Silent 23 20030537 G A 33 58 LUAD TCGA-17-Z056 MAP7D2 SNP Splice_site 23 20074798 C A 21 73 LUAD TCGA-17-Z060 MAP7D2 SNP Splice_site 23 20082923 C G 26 52 LUSC TCGA-18-5595 MAP7D2 SNP Missense_Mutation 23 20030525 C T 29 75 LUSC TCGA-21-1071 MAP7D2 SNP Missense_Mutation 23 20033400 G A 38 71 LUAD TCGA-49-4501 MAP7D2 SNP Missense_Mutation 23 20031731 T G 52 73 LUAD TCGA-49-4505 MAP7D2 SNP Missense_Mutation 23 20034374 C A 28 44 LUAD TCGA-64-1677 MAP7D2 SNP Missense_Mutation 23 20043822 C T 30 55 LUSC TCGA-66-2800 MAP7D2 SNP Missense_Mutation 23 20030581 T C 58 77 LUSC TCGA-66-2800 MAP7D2 SNP Missense_Mutation 23 20034289 G A 38 41 GBM TCGA-87-5896 MAP7D2 SNP Silent 23 20074865 C T 28 70 LUAD TCGA-91-6836 MAP7D2 SNP Silent 23 20070999 G T 39 61 BRCA TCGA-A2-A0YT MAP7D2 SNP Missense_Mutation 23 20070998 C G 31 55 KIRC TCGA-A3-3385 MAP7D2 SNP Nonsense_Mutation 23 20081684 G A 46 67 UCEC TCGA-A5-A0GP MAP7D2 SNP Missense_Mutation 23 20034378 C T 31 56 UCEC TCGA-A5-A0VP MAP7D2 SNP Missense_Mutation 23 20033417 T C 54 73 UCEC TCGA-A5-A0VP MAP7D2 SNP Silent 23 20043896 G A 42 45 CRC TCGA-AA-3554 MAP7D2 SNP Missense_Mutation 23 20071061 G A 40 50 CRC TCGA-AA-3672 MAP7D2 SNP Missense_Mutation 23 20074902 A G 7 73 CRC TCGA-AA-3845 MAP7D2 DEL Frame_Shift_Del 23 20060663 A - 9 52 CRC TCGA-AA-3966 MAP7D2 DEL Frame_Shift_Del 23 20043807 T - 60 45 CRC TCGA-AA-3977 MAP7D2 SNP Missense_Mutation 23 20034397 G A 37 57 AML TCGA-AB-2806 MAP7D2 SNP Missense_Mutation 23 20033438 G A 46 54 AML TCGA-AB-2919 MAP7D2 SNP Silent 23 20033425 C T 24 54 CRC TCGA-AG-3892 MAP7D2 SNP Silent 23 20028972 G A 37 43 CRC TCGA-AG-A002 MAP7D2 SNP Missense_Mutation 23 20031204 T C 56 60 CRC TCGA-AG-A002 MAP7D2 SNP Missense_Mutation 23 20034397 G A 37 57 CRC TCGA-AG-A002 MAP7D2 SNP Nonsense_Mutation 23 20062574 G A 37 58 UCEC TCGA-AP-A051 MAP7D2 SNP Missense_Mutation 23 20043997 G A 39 66 UCEC TCGA-AP-A051 MAP7D2 SNP Missense_Mutation 23 20071040 C T 27 65 UCEC TCGA-AP-A056 MAP7D2 SNP Missense_Mutation 23 20028971 C T 31 78 UCEC TCGA-AP-A056 MAP7D2 SNP Missense_Mutation 23 20029055 G T 33 70 UCEC TCGA-AP-A056 MAP7D2 SNP Silent 23 20030502 A G 8 50 UCEC TCGA-AP-A059 MAP7D2 SNP Missense_Mutation 23 20028938 G A 33 78 UCEC TCGA-AP-A0LM MAP7D2 SNP Missense_Mutation 23 20060677 C T 32 48 UCEC TCGA-AP-A0LM MAP7D2 SNP Missense_Mutation 23 20081543 G A 39 66 UCEC TCGA-AP-A0LM MAP7D2 SNP Missense_Mutation 23 20082869 C T 31 92 UCEC TCGA-AX-A05Z MAP7D2 SNP Nonsense_Mutation 23 20043079 C A 32 59 UCEC TCGA-AX-A06L MAP7D2 SNP Missense_Mutation 23 20071000 G C 44 52 UCEC TCGA-AX-A0J0 MAP7D2 SNP Missense_Mutation 23 20028927 G T 33 54 UCEC TCGA-AX-A0J0 MAP7D2 SNP Missense_Mutation 23 20030576 A C 1 65 UCEC TCGA-AX-A0J0 MAP7D2 SNP Missense_Mutation 23 20034397 G A 37 57 KIRC TCGA-B0-5702 MAP7D2 SNP Splice_Site 23 20074911 T C 53 86 UCEC TCGA-B5-A0JY MAP7D2 SNP Missense_Mutation 23 20060710 G T 33 78 UCEC TCGA-B5-A11E MAP7D2 SNP Silent 23 20043149 G A 33 65 UCEC TCGA-B5-A11N MAP7D2 SNP Missense_Mutation 23 20028971 C T 31 78 UCEC TCGA-B5-A11N MAP7D2 SNP Silent 23 20033395 G A 37 46 UCEC TCGA-B5-A11R MAP7D2 SNP Missense_Mutation 23 20033383 C G 32 51 BRCA TCGA-BH-A0AW MAP7D2 SNP Silent 23 20030640 C T 29 59 UCEC TCGA-BK-A13C MAP7D2 SNP Missense_Mutation 23 20071071 G T 42 65 KIRC TCGA-BP-4803 MAP7D2 SNP Missense_Mutation 23 20060638 G A 33 66 UCEC TCGA-BS-A0UF MAP7D2 SNP Missense_Mutation 23 20074839 G A 37 78 UCEC TCGA-BS-A0UV MAP7D2 SNP Missense_Mutation 23 20034378 C T 31 56 UCEC TCGA-BS-A0UV MAP7D2 SNP Nonsense_Mutation 23 20060723 G A 40 51 HNSC TCGA-CR-7394 MAP7D2 SNP Missense_Mutation 23 20033405 T G 55 60 HNSC TCGA-CV-7421 MAP7D2 SNP Missense_Mutation 23 20043130 G T 48 77 UCEC TCGA-D1-A103 MAP7D2 SNP Missense_Mutation 23 20043939 C T 28 56 UCEC TCGA-D1-A16Y MAP7D2 SNP Nonsense_Mutation 23 20033442 C A 32 94 UCEC TCGA-D1-A177 MAP7D2 SNP Missense_Mutation 23 20043906 T C 55 55 UCEC TCGA-D1-A177 MAP7D2 SNP Missense_Mutation 23 20068979 T G 54 67 UCEC TCGA-D1-A17Q MAP7D2 SNP Missense_Mutation 23 20029058 C A 32 93 UCEC TCGA-D1-A17Q MAP7D2 SNP Silent 23 20043155 C T 31 49 HNSC TCGA-DQ-5631 MAP7D2 SNP Silent 23 20082895 C T 32 60 BRCA TCGA-E9-A1RH MAP7D2 SNP Missense_Mutation 23 20069029 G C 33 57