ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62854 WDR5B SNP Nonsense 3 122133783 G C 45 80 MEL MEL-JWCI-WGS-11 WDR5B SNP Missense_Mutation 3 122133735 G A 33 75 OV TCGA-13-0912 WDR5B SNP Missense_Mutation 3 122133514 C G 32 93 OV TCGA-13-1482 WDR5B SNP Missense_Mutation 3 122133656 G T 46 60 OV TCGA-24-1418 WDR5B SNP Missense_Mutation 3 122133816 T C 49 83 LUAD TCGA-44-3398 WDR5B SNP Missense_Mutation 3 122134359 G A 45 56 LUSC TCGA-56-6545 WDR5B SNP Missense_Mutation 3 122134320 G A 42 64 CRC TCGA-AA-3846 WDR5B SNP Silent 3 122134076 A T 7 49 CRC TCGA-AA-A010 WDR5B SNP Missense_Mutation 3 122133685 C T 30 68 CRC TCGA-AA-A01K WDR5B SNP Missense_Mutation 3 122133703 T G 51 54 CRC TCGA-AF-3913 WDR5B SNP Missense_Mutation 3 122133553 C T 31 93 KIRC TCGA-B0-4694 WDR5B SNP Silent 3 122133767 T C 64 55 KIRC TCGA-BP-4989 WDR5B SNP Missense_Mutation 3 122134164 T C 49 64 UCEC TCGA-BS-A0UF WDR5B SNP Silent 3 122134001 A G 14 57 HNSC TCGA-CR-7369 WDR5B SNP Missense_Mutation 3 122133906 C T 30 87 KIRC TCGA-CZ-4859 WDR5B SNP Silent 3 122133533 A T 1 51 UCEC TCGA-D1-A16X WDR5B SNP Missense_Mutation 3 122134062 T G 64 71