ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-102 PSAT1 SNP Silent 9 80919828 C T 31 47 MEL MEL-Ma-Mel-114 PSAT1 SNP Missense_Mutation 9 80921241 C T 30 74 LUAD TCGA-05-4396 PSAT1 SNP Missense_Mutation 9 80921263 C A 21 99 LUAD TCGA-05-4396 PSAT1 SNP Silent 9 80921330 C A 23 39 LUAD TCGA-05-4396 PSAT1 SNP Silent 9 80943903 G T 47 52 GBM TCGA-06-0139 PSAT1 SNP Missense_Mutation 9 80921319 G A 45 59 GBM TCGA-06-0139 PSAT1 SNP Missense_Mutation 9 80921343 G A 34 68 LUAD TCGA-17-Z028 PSAT1 SNP Missense_Mutation 9 80919661 G T 33 84 OV TCGA-23-1031 PSAT1 DEL Frame_Shift_Del 9 80943096 AGGGCAT - 3 64 LUSC TCGA-33-4583 PSAT1 SNP Missense_Mutation 9 80919698 G A 46 51 LUSC TCGA-46-6025 PSAT1 SNP Missense_Mutation 9 80923366 G A 47 100 LUSC TCGA-85-6561 PSAT1 SNP Nonsense_Mutation 9 80921340 G T 43 88 KIRC TCGA-A3-3323 PSAT1 SNP Missense_Mutation 9 80923397 G A 40 100 CRC TCGA-AA-3672 PSAT1 SNP Missense_Mutation 9 80923337 T C 59 80 CRC TCGA-AA-A00J PSAT1 SNP Missense_Mutation 9 80919698 G A 46 51 CRC TCGA-AA-A00K PSAT1 SNP Missense_Mutation 9 80916929 C T 27 70 CRC TCGA-AG-A002 PSAT1 SNP Missense_Mutation 9 80916919 G T 33 66 UCEC TCGA-AP-A059 PSAT1 SNP Silent 9 80919840 A G 2 59 UCEC TCGA-AP-A059 PSAT1 SNP Silent 9 80923405 C T 24 69 UCEC TCGA-AP-A0LM PSAT1 SNP Missense_Mutation 9 80921331 G A 37 100 UCEC TCGA-B5-A0JY PSAT1 SNP Missense_Mutation 9 80943058 C A 32 62 UCEC TCGA-B5-A11E PSAT1 SNP Missense_Mutation 9 80932644 G A 38 63 UCEC TCGA-BS-A0UF PSAT1 SNP Missense_Mutation 9 80916919 G T 33 66 UCEC TCGA-BS-A0UV PSAT1 SNP Missense_Mutation 9 80921233 T C 52 90 BLCA TCGA-BT-A3PH PSAT1 SNP Splice_site 9 80912185 C G 29 91 UCEC TCGA-D1-A0ZS PSAT1 SNP Silent 9 80932598 C T 19 48 UCEC TCGA-D1-A167 PSAT1 SNP Missense_Mutation 9 80916876 G A 36 100 UCEC TCGA-D1-A17H PSAT1 SNP Silent 9 80923441 C T 24 56