ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-RT-S01831 RAET1G SNP Missense_Mutation 6 150240719 C G 29 51 LUAD LUAD-S01315 RAET1G SNP Missense_Mutation 6 150240319 C G 30 37 LUAD LUAD-S01346 RAET1G SNP Missense_Mutation 6 150244118 A G 3 45 MEL ME009 RAET1G SNP Silent 6 150240195 C T 21 50 MEL MEL-13560 RAET1G SNP Silent 6 150240765 G A 44 32 LUAD TCGA-05-4396 RAET1G SNP Silent 6 150240693 G T 47 51 LUAD TCGA-05-5428 RAET1G SNP Silent 6 150240366 G A 41 49 LUSC TCGA-22-5473 RAET1G SNP Missense_Mutation 6 150240831 C G 32 35 GBM TCGA-32-5222 RAET1G SNP Missense_Mutation 6 150240886 G A 38 50 LUSC TCGA-34-2596 RAET1G SNP Missense_Mutation 6 150240389 G A 34 50 LUSC TCGA-51-4081 RAET1G SNP Silent 6 150239492 G T 43 54 CRC TCGA-AA-A00J RAET1G SNP Silent 6 150240411 T A 58 50 CRC TCGA-AG-A02N RAET1G SNP Silent 6 150240885 C T 23 42 KIRC TCGA-AK-3444 RAET1G SNP Silent 6 150240945 G A 36 50 UCEC TCGA-AP-A0LM RAET1G SNP Missense_Mutation 6 150238089 C T 27 41 UCEC TCGA-AP-A0LM RAET1G SNP Missense_Mutation 6 150239478 G A 40 52 KIRC TCGA-AS-3778 RAET1G SNP Missense_Mutation 6 150240312 T A 62 47 UCEC TCGA-AX-A0J0 RAET1G SNP Missense_Mutation 6 150240291 C A 32 50 UCEC TCGA-B5-A11E RAET1G SNP Missense_Mutation 6 150240332 T C 60 49 UCEC TCGA-BS-A0UM RAET1G SNP Missense_Mutation 6 150239488 G T 44 41 HNSC TCGA-CN-5358 RAET1G SNP Silent 6 150240360 G C 33 53 HNSC TCGA-CN-5360 RAET1G SNP Missense_Mutation 6 150240901 C T 30 51 BLCA TCGA-CU-A0YR RAET1G SNP Missense_Mutation 6 150240778 C A 21 55 HNSC TCGA-CV-7253 RAET1G SNP Missense_Mutation 6 150240749 C A 18 47 UCEC TCGA-D1-A103 RAET1G SNP Silent 6 150240218 A G 3 45 UCEC TCGA-D1-A167 RAET1G SNP Silent 6 150238090 G A 38 52 UCEC TCGA-D1-A17Q RAET1G SNP Silent 6 150238093 G A 40 41 BRCA TCGA-E2-A159 RAET1G SNP Silent 6 150240756 C T 29 55 BRCA TCGA-E9-A1NA RAET1G SNP Silent 6 150239333 C G 29 27