ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-059 TSPYL1 SNP Missense_Mutation 6 116599741 C A 31 71 MEL MEL-JWCI-WGS-23 TSPYL1 SNP Silent 6 116600823 G C 37 46 MM MM-0544 TSPYL1 SNP Nonsense_Mutation 6 116600331 C T 26 52 OV TCGA-04-1337 TSPYL1 SNP Nonsense_Mutation 6 116600321 C A 29 37 LUAD TCGA-05-4396 TSPYL1 SNP Silent 6 116600166 C A 23 43 LUAD TCGA-17-Z022 TSPYL1 SNP Missense_Mutation 6 116600261 G C 45 72 LUAD TCGA-17-Z056 TSPYL1 SNP Missense_Mutation 6 116600644 G A 42 56 LUSC TCGA-22-1016 TSPYL1 SNP Missense_Mutation 6 116600879 G T 47 51 OV TCGA-36-1577 TSPYL1 SNP Nonsense_Mutation 6 116600085 G C 48 56 BRCA TCGA-A1-A0SO TSPYL1 SNP Missense_Mutation 6 116599945 G C 33 72 CRC TCGA-AA-3715 TSPYL1 SNP Missense_Mutation 6 116600272 G A 36 72 CRC TCGA-AG-A002 TSPYL1 SNP Missense_Mutation 6 116600075 A C 1 50 UCEC TCGA-AP-A0LM TSPYL1 SNP Missense_Mutation 6 116600097 C A 32 50 KIRC TCGA-B0-5106 TSPYL1 DEL Frame_Shift_Del 6 116599803 TT - 56 53 UCEC TCGA-BK-A0CC TSPYL1 SNP Missense_Mutation 6 116600417 C T 32 72 KIRC TCGA-BP-4338 TSPYL1 SNP Missense_Mutation 6 116600312 G T 39 62 BLCA TCGA-BT-A20O TSPYL1 SNP Missense_Mutation 6 116600201 G C 35 72 BRCA TCGA-C8-A1HE TSPYL1 SNP Missense_Mutation 6 116600543 C T 29 40 KIRC TCGA-CJ-5686 TSPYL1 DEL Frame_Shift_Del 6 116600703 C - 26 50 HNSC TCGA-CR-6472 TSPYL1 SNP Missense_Mutation 6 116599934 G C 41 72 UCEC TCGA-D1-A15X TSPYL1 SNP Missense_Mutation 6 116600626 T C 56 47 UCEC TCGA-D1-A163 TSPYL1 SNP Missense_Mutation 6 116599879 T C 58 54 BLCA TCGA-DK-A3IV TSPYL1 SNP Missense_Mutation 6 116600209 C G 31 72