ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-179 LYPD6B SNP Missense_Mutation 2 150069620 G A 37 46 HNSC HN_63021 LYPD6B SNP Missense 2 150071080 A C 3 57 LUAD LUAD-TLLGS LYPD6B SNP Silent 2 150061800 C G 29 77 MEL MEL-UKRV-Mel-24 LYPD6B SNP Missense_Mutation 2 150069548 G A 41 86 MM MM-0456-SWAP LYPD6B SNP Missense_Mutation 2 150064872 G A 38 87 LUAD TCGA-05-4396 LYPD6B SNP Splice_site 2 150069636 G T 39 49 LUAD TCGA-05-4432 LYPD6B SNP Silent 2 150061878 C A 21 58 LUAD TCGA-17-Z010 LYPD6B SNP Missense_Mutation 2 150071214 C T 21 50 OV TCGA-30-1862 LYPD6B SNP Missense_Mutation 2 150069509 C T 17 85 LUAD TCGA-64-5775 LYPD6B SNP Missense_Mutation 2 150069541 A T 7 60 LUAD TCGA-67-3771 LYPD6B SNP Missense_Mutation 2 150071151 G C 33 86 UCEC TCGA-A5-A0GB LYPD6B SNP Missense_Mutation 2 150061828 G A 38 57 CRC TCGA-AA-3984 LYPD6B SNP Missense_Mutation 2 150061778 C T 31 51 CRC TCGA-AG-3892 LYPD6B SNP Silent 2 150071119 T G 53 31 UCEC TCGA-AP-A056 LYPD6B SNP Missense_Mutation 2 150064911 A G 5 68 UCEC TCGA-AX-A063 LYPD6B SNP Missense_Mutation 2 150071219 C A 28 55 UCEC TCGA-AX-A0J0 LYPD6B SNP Missense_Mutation 2 150064872 G A 38 87 UCEC TCGA-B5-A0JY LYPD6B SNP Missense_Mutation 2 150061778 C T 31 51 UCEC TCGA-BS-A0UF LYPD6B SNP Missense_Mutation 2 150061912 C A 32 59 UCEC TCGA-BS-A0UV LYPD6B SNP Missense_Mutation 2 150017338 C A 32 49 BLCA TCGA-CU-A3KJ LYPD6B SNP Silent 2 150071149 G A 33 62 UCEC TCGA-D1-A103 LYPD6B SNP Missense_Mutation 2 150061828 G A 38 57 HNSC TCGA-D6-6516 LYPD6B SNP Missense_Mutation 2 150071213 C T 30 73