ttype patient gene classification type chr pos ref_allele newbase context65 cons46 OV TCGA-23-1022 SHARPIN SNP Missense_Mutation 8 145153859 G A 43 50 LUAD TCGA-50-5935 SHARPIN SNP Missense_Mutation 8 145158011 G C 45 54 OV TCGA-61-1728 SHARPIN SNP Nonsense_Mutation 8 145153890 C T 21 73 LUSC TCGA-66-2767 SHARPIN SNP Missense_Mutation 8 145154057 C T 27 48 BRCA TCGA-AN-A0XP SHARPIN SNP Silent 8 145154196 A C 11 52 UCEC TCGA-AP-A051 SHARPIN SNP Splice_Site 8 145157953 C T 18 73 KIRC TCGA-B0-4707 SHARPIN SNP Missense_Mutation 8 145154874 C T 29 52 BRCA TCGA-BH-A0H5 SHARPIN SNP Silent 8 145154289 G A 45 54 KIRC TCGA-BP-4163 SHARPIN SNP Missense_Mutation 8 145154959 G C 36 53 UCEC TCGA-BS-A0UJ SHARPIN SNP Missense_Mutation 8 145153828 T G 59 67 HNSC TCGA-CQ-6224 SHARPIN SNP Silent 8 145154029 G A 43 49 HNSC TCGA-CV-7406 SHARPIN SNP Silent 8 145154328 G A 33 58 HNSC TCGA-D6-6824 SHARPIN SNP Silent 8 145154650 C G 29 50