ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls297 WNT2B SNP Missense_Mutation 1 113052041 C T 26 71 ESO ESO-913 WNT2B SNP Missense_Mutation 1 113057692 G A 40 99 MEL ME043 WNT2B SNP Silent 1 113059949 G A 41 51 MEL MEL-JWCI-WGS-32 WNT2B SNP Missense_Mutation 1 113057539 C T 22 84 GBM TCGA-02-2485 WNT2B DEL Frame_Shift_Del 1 113059824 CT - 20 72 LUAD TCGA-05-4396 WNT2B SNP Silent 1 113057614 C A 23 71 LUAD TCGA-17-Z001 WNT2B SNP Splice_Site 1 113033704 G T 44 33 LUAD TCGA-17-Z060 WNT2B SNP Missense_Mutation 1 113059924 G A 38 73 LUSC TCGA-21-5787 WNT2B SNP Missense_Mutation 1 113058889 T A 51 52 OV TCGA-25-2042 WNT2B SNP Missense_Mutation 1 113059875 G T 42 100 LUSC TCGA-37-3783 WNT2B SNP Missense_Mutation 1 113059968 G C 45 100 LUSC TCGA-60-2710 WNT2B SNP Missense_Mutation 1 113059863 C T 19 81 UCEC TCGA-A5-A0GP WNT2B SNP Missense_Mutation 1 113059774 A C 3 91 CRC TCGA-AA-A010 WNT2B SNP Missense_Mutation 1 113057648 G A 38 85 CRC TCGA-AG-3902 WNT2B SNP Missense_Mutation 1 113057699 G C 42 99 CRC TCGA-AG-A002 WNT2B SNP Nonsense_Mutation 1 113057614 C T 23 71 UCEC TCGA-AP-A0LD WNT2B SNP Missense_Mutation 1 113058897 G A 40 66 UCEC TCGA-AP-A0LM WNT2B SNP Silent 1 113057667 T C 57 77 UCEC TCGA-AP-A0LM WNT2B SNP Missense_Mutation 1 113059864 G A 38 80 BRCA TCGA-AR-A250 WNT2B SNP Silent 1 113058811 C A 30 48 BRCA TCGA-B6-A0RI WNT2B SNP Missense_Mutation 1 113057615 G A 37 66 UCEC TCGA-BS-A0TJ WNT2B SNP Silent 1 113059841 C T 25 59 UCEC TCGA-BS-A0UF WNT2B SNP Missense_Mutation 1 113051927 C T 28 55 UCEC TCGA-BS-A0UF WNT2B SNP Nonsense_Mutation 1 113057518 C T 19 67 UCEC TCGA-BS-A0UV WNT2B SNP Missense_Mutation 1 113063059 G T 35 59 BRCA TCGA-C8-A275 WNT2B SNP Silent 1 113057694 C T 32 57 UCEC TCGA-D1-A0ZO WNT2B SNP Silent 1 113052049 C T 27 50 UCEC TCGA-D1-A103 WNT2B SNP Silent 1 113057626 C A 23 66 UCEC TCGA-D1-A15X WNT2B SNP Missense_Mutation 1 113057648 G A 38 85 UCEC TCGA-D1-A16X WNT2B SNP Missense_Mutation 1 113057617 G A 33 84 BRCA TCGA-D8-A1JL WNT2B SNP Missense_Mutation 1 113057692 G A 40 99 BLCA TCGA-DK-A2I4 WNT2B SNP Silent 1 113058964 C T 31 51 BRCA TCGA-E2-A108 WNT2B SNP Silent 1 113052034 G C 45 57