ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW194 SFRS2 SNP Missense_Mutation 17 74732921 G T 39 77 DLBCL DLBCL-LS4592 SFRS2 SNP Missense_Mutation 17 74732968 T G 57 68 DLBCL DLBCL-Ls2596 SFRS2 SNP Silent 17 74732973 C T 27 54 LUAD LUAD-D02185 SFRS2 SNP Silent 17 74732492 G A 46 49 LUAD LUAD-YINHD SFRS2 SNP Missense_Mutation 17 74732542 T A 53 59 LUAD TCGA-05-4403 SFRS2 SNP Silent 17 74733003 C G 21 52 GBM TCGA-06-0189 SFRS2 SNP Missense_Mutation 17 74732284 G T 41 71 LUSC TCGA-37-4133 SFRS2 SNP Missense_Mutation 17 74732326 C G 20 59 LUSC TCGA-66-2773 SFRS2 SNP Missense_Mutation 17 74732373 G C 33 89 LUSC TCGA-66-2773 SFRS2 SNP Silent 17 74733066 G A 37 70 AML TCGA-AB-2805 SFRS2 SNP Missense_Mutation 17 74732959 G A 43 75 AML TCGA-AB-2810 SFRS2 SNP Missense_Mutation 17 74732959 G T 43 75 AML TCGA-AB-2850 SFRS2 DEL In_Frame_Del 17 74732936 GGCGGCTGTGGTGTGAGTCCGGGG - 39 55 AML TCGA-AB-2959 SFRS2 SNP Missense_Mutation 17 74732959 G A 43 75 CRC TCGA-AG-A002 SFRS2 SNP Missense_Mutation 17 74732349 G T 33 83 BRCA TCGA-BH-A1EV SFRS2 SNP Missense_Mutation 17 74732502 G C 41 84 KIRC TCGA-BP-4167 SFRS2 SNP Silent 17 74732441 T C 50 43 BLCA TCGA-BT-A3PJ SFRS2 SNP Missense_Mutation 17 74732409 C T 31 76 HNSC TCGA-CV-6962 SFRS2 SNP Missense_Mutation 17 74732524 G C 39 59 KIRC TCGA-CZ-5457 SFRS2 SNP Nonsense_Mutation 17 74732524 G A 39 59 UCEC TCGA-D1-A0ZN SFRS2 SNP Missense_Mutation 17 74733188 C T 30 96 HNSC TCGA-D6-6516 SFRS2 SNP Missense_Mutation 17 74732409 C A 31 76 BLCA TCGA-FD-A3B5 SFRS2 SNP Missense_Mutation 17 74732295 C A 31 71 BLCA TCGA-G2-A2EO SFRS2 SNP Missense_Mutation 17 74732523 C A 31 75