ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1133 SYPL2 SNP Missense_Mutation 1 110019406 G T 39 56 ESO ESO-1163 SYPL2 SNP Nonsense_Mutation 1 110022087 C T 21 56 HNSC HN_62739 SYPL2 SNP Synonymous 1 110009477 C A 23 49 LUAD LUAD-S01413 SYPL2 SNP Missense_Mutation 1 110020608 A G 16 59 LUAD LUAD_E00565 SYPL2 SNP Missense_Mutation 1 110022120 G T 43 71 MEL MEL-JWCI-WGS-19 SYPL2 SNP Silent 1 110019497 C T 31 51 LUAD TCGA-05-4396 SYPL2 SNP Silent 1 110022032 C A 23 49 LUAD TCGA-05-4432 SYPL2 SNP Missense_Mutation 1 110018245 G T 39 96 LUAD TCGA-17-Z003 SYPL2 SNP Missense_Mutation 1 110018304 C G 31 48 LUAD TCGA-17-Z025 SYPL2 SNP Missense_Mutation 1 110022016 A G 2 78 LUAD TCGA-17-Z026 SYPL2 SNP Silent 1 110022119 G A 35 72 OV TCGA-25-2392 SYPL2 SNP Silent 1 110019431 C T 27 50 LUAD TCGA-44-2668 SYPL2 SNP Silent 1 110019410 C A 30 51 LUAD TCGA-73-4676 SYPL2 SNP Missense_Mutation 1 110019462 C A 24 76 CRC TCGA-AA-3984 SYPL2 SNP Nonsense_Mutation 1 110020565 C A 26 66 CRC TCGA-AA-A010 SYPL2 SNP Missense_Mutation 1 110022017 C A 20 77 AML TCGA-AB-2929 SYPL2 SNP Silent 1 110019500 G A 45 52 CRC TCGA-AG-3727 SYPL2 SNP Missense_Mutation 1 110018224 G A 39 83 BRCA TCGA-AO-A0JJ SYPL2 SNP Missense_Mutation 1 110020512 G A 37 100 UCEC TCGA-AP-A051 SYPL2 SNP Silent 1 110018265 T C 62 53 UCEC TCGA-AP-A054 SYPL2 SNP Silent 1 110019434 T C 51 37 UCEC TCGA-AP-A056 SYPL2 SNP Missense_Mutation 1 110019591 C A 22 85 UCEC TCGA-AP-A059 SYPL2 SNP Missense_Mutation 1 110019476 C A 32 59 UCEC TCGA-AP-A0LM SYPL2 SNP Missense_Mutation 1 110020445 C A 32 66 UCEC TCGA-AX-A0J0 SYPL2 SNP Missense_Mutation 1 110020512 G A 37 100 HNSC TCGA-BA-4076 SYPL2 SNP Missense_Mutation 1 110022063 C A 22 67 KIRC TCGA-BP-4976 SYPL2 SNP Missense_Mutation 1 110020593 G C 39 87 BRCA TCGA-C8-A131 SYPL2 SNP Silent 1 110018244 C T 27 49 HNSC TCGA-CR-7371 SYPL2 SNP Missense_Mutation 1 110020605 T A 54 65 HNSC TCGA-CV-5976 SYPL2 SNP Silent 1 110022065 G C 40 32 UCEC TCGA-D1-A16F SYPL2 SNP Silent 1 110019440 G A 36 44