ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-S00488 SPRR2E SNP Silent 1 153066192 G A 42 55 LUAD LUAD_E00522 SPRR2E SNP Missense_Mutation 1 153066052 G T 35 49 MEL MEL-JWCI-WGS-34 SPRR2E SNP Missense_Mutation 1 153066145 G A 47 61 MEL MEL-Ma-Mel-37 SPRR2E SNP Splice_site 1 153066228 C T 30 55 MEL MEL-Ma-Mel-85 SPRR2E SNP Silent 1 153066096 G A 35 32 LUAD TCGA-05-4427 SPRR2E SNP Missense_Mutation 1 153066193 C G 25 71 OV TCGA-13-0904 SPRR2E SNP Silent 1 153066108 C T 20 52 LUAD TCGA-35-4122 SPRR2E SNP Missense_Mutation 1 153066017 T C 54 57 LUAD TCGA-44-2656 SPRR2E SNP Missense_Mutation 1 153066043 G T 43 51 LUAD TCGA-49-6743 SPRR2E SNP Missense_Mutation 1 153066113 G T 44 52 LUAD TCGA-50-5930 SPRR2E SNP Missense_Mutation 1 153066140 G T 43 61 CRC TCGA-AA-A010 SPRR2E SNP Silent 1 153066099 C T 28 54 CRC TCGA-AA-A02H SPRR2E SNP Missense_Mutation 1 153066212 G T 46 49 CRC TCGA-AG-A01L SPRR2E SNP Missense_Mutation 1 153066193 C A 25 71 UCEC TCGA-AP-A056 SPRR2E SNP Silent 1 153066117 T C 59 42 UCEC TCGA-AP-A0LM SPRR2E SNP Silent 1 153066120 G A 42 41 UCEC TCGA-B5-A0JY SPRR2E SNP Missense_Mutation 1 153066018 C A 32 53 UCEC TCGA-B5-A0K6 SPRR2E SNP Missense_Mutation 1 153066223 G T 33 60 HNSC TCGA-BB-4223 SPRR2E SNP Missense_Mutation 1 153066128 C G 29 60 UCEC TCGA-BG-A0M4 SPRR2E SNP Missense_Mutation 1 153066122 A G 7 58 UCEC TCGA-BS-A0UJ SPRR2E SNP Missense_Mutation 1 153066134 A G 6 68