ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0043 RAET1E SNP Missense_Mutation 6 150211113 C G 28 52 BRCA BR-MEX-076 RAET1E SNP Splice_site 6 150209805 T A 53 55 CLL CW56-PRE RAET1E SNP Missense_Mutation 6 150211980 G T 34 51 DLBCL DLBCL-Ls1065 RAET1E SNP Missense_Mutation 6 150211236 C G 32 49 LUAD LUAD-CHTN-Z4716A RAET1E SNP Missense_Mutation 6 150210691 G T 46 31 LUAD LUAD-RT-S01707 RAET1E SNP Missense_Mutation 6 150209773 C A 21 50 MEL MEL-JWCI-WGS-39 RAET1E SNP Silent 6 150211025 G A 47 52 LUAD TCGA-05-4396 RAET1E SNP Nonsense_Mutation 6 150210739 C A 31 42 LUAD TCGA-05-4410 RAET1E SNP Missense_Mutation 6 150210584 G C 48 53 LUAD TCGA-17-Z014 RAET1E SNP Nonsense_Mutation 6 150209691 A T 6 46 KIRC TCGA-A3-3387 RAET1E SNP Missense_Mutation 6 150210680 G A 47 44 CRC TCGA-AA-3973 RAET1E SNP Missense_Mutation 6 150210703 C T 21 52 CRC TCGA-AA-3977 RAET1E SNP Missense_Mutation 6 150211143 C T 26 52 CRC TCGA-AG-A002 RAET1E SNP Silent 6 150210578 C T 26 20 UCEC TCGA-AP-A0LM RAET1E SNP Missense_Mutation 6 150209789 C T 25 35 KIRC TCGA-B0-4811 RAET1E SNP Silent 6 150211277 A G 10 50 UCEC TCGA-B5-A11Y RAET1E SNP Missense_Mutation 6 150210538 C T 31 48 BLCA TCGA-BT-A3PH RAET1E SNP Missense_Mutation 6 150210659 G C 33 40 BRCA TCGA-C8-A26V RAET1E SNP Missense_Mutation 6 150211130 C G 32 70 HNSC TCGA-CN-5365 RAET1E SNP Missense_Mutation 6 150210664 G T 35 54 HNSC TCGA-CR-7380 RAET1E DEL Frame_Shift_Del 6 150209677 T - 52 32 HNSC TCGA-CV-7099 RAET1E SNP Silent 6 150210518 G A 33 55 HNSC TCGA-CV-7099 RAET1E SNP Missense_Mutation 6 150210686 G A 37 49 BLCA TCGA-DK-A3IS RAET1E SNP Silent 6 150209697 G A 45 48 BLCA TCGA-DK-A3IS RAET1E SNP Silent 6 150210554 G C 33 45