ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CLL_080 HHATL SNP Missense_Mutation 3 42734301 C T 19 58 LUAD LUAD-B00523 HHATL SNP Nonsense_Mutation 3 42735130 C T 22 59 LUAD LUAD-B01024 HHATL SNP Missense_Mutation 3 42739045 G T 43 98 LUAD LUAD-RT-S01301 HHATL SNP Missense_Mutation 3 42739670 G T 37 51 LUAD LUAD-S00488 HHATL SNP Silent 3 42735211 A G 3 50 MEL ME049 HHATL SNP Splice_Site 3 42738999 C T 18 97 MEL MEL-JWCI-WGS-29 HHATL SNP Missense_Mutation 3 42735116 C T 31 51 MEL MEL-JWCI-WGS-8 HHATL SNP Silent 3 42739793 C T 22 51 MEL MEL-Ma-Mel-105 HHATL SNP Silent 3 42739055 G A 41 59 MEL MEL-Ma-Mel-37 HHATL SNP Silent 3 42734594 C T 21 51 OV TCGA-13-0885 HHATL SNP Missense_Mutation 3 42734256 T C 54 55 LUAD TCGA-17-Z047 HHATL SNP Silent 3 42734573 G C 45 46 LUSC TCGA-18-3409 HHATL SNP Silent 3 42738546 C T 21 73 OV TCGA-20-0991 HHATL SNP Missense_Mutation 3 42739827 C T 26 86 OV TCGA-25-1317 HHATL SNP Missense 3 42734605 A G 4 83 OV TCGA-29-2427 HHATL SNP Missense_Mutation 3 42738341 G T 34 96 LUAD TCGA-35-3621 HHATL SNP Silent 3 42740356 A G 7 34 LUAD TCGA-44-2655 HHATL SNP Missense_Mutation 3 42739015 G T 43 64 LUAD TCGA-44-2656 HHATL SNP Splice_site 3 42738369 C A 26 52 BRCA TCGA-A2-A25A HHATL SNP Silent 3 42740389 G T 34 68 UCEC TCGA-A5-A0G9 HHATL SNP Splice_site 3 42739634 C A 24 75 CRC TCGA-AA-3555 HHATL SNP Missense_Mutation 3 42739807 C T 18 63 CRC TCGA-AA-A010 HHATL SNP Missense_Mutation 3 42739081 C T 31 98 UCEC TCGA-AP-A056 HHATL SNP Missense_Mutation 3 42735299 T C 60 88 UCEC TCGA-AP-A059 HHATL SNP Missense_Mutation 3 42741285 C T 17 62 UCEC TCGA-AP-A059 HHATL SNP Missense_Mutation 3 42742233 C T 26 65 UCEC TCGA-AP-A0LM HHATL SNP Missense_Mutation 3 42739798 G T 45 72 UCEC TCGA-AX-A05S HHATL SNP Missense_Mutation 3 42739794 C A 22 99 UCEC TCGA-AX-A0J1 HHATL SNP Silent 3 42734297 C T 28 54 UCEC TCGA-B5-A11N HHATL SNP Missense_Mutation 3 42740595 G A 37 65 KIRC TCGA-B8-5551 HHATL SNP Missense_Mutation 3 42734320 C T 19 72 UCEC TCGA-BS-A0UF HHATL SNP Silent 3 42734255 C A 32 51 UCEC TCGA-BS-A0UV HHATL SNP Missense_Mutation 3 42735116 C T 31 51 UCEC TCGA-BS-A0UV HHATL SNP Missense_Mutation 3 42739081 C T 31 98 UCEC TCGA-BS-A0UV HHATL SNP Silent 3 42740545 G A 33 70 UCEC TCGA-BS-A0UV HHATL SNP Missense_Mutation 3 42742307 C A 32 64 HNSC TCGA-CR-7383 HHATL SNP Missense_Mutation 3 42739102 C T 19 62 BLCA TCGA-DK-A3IK HHATL DEL In_Frame_Del 3 42740315 AGC - 3 79 BLCA TCGA-GV-A3JZ HHATL SNP Missense_Mutation 3 42734575 G A 36 69