ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUSC TCGA-34-2600 HNRNPD SNP Nonsense_Mutation 4 83278594 C A 30 98 LUAD TCGA-44-2656 HNRNPD DEL Frame_Shift_Del 4 83278025 C - 31 40 CRC TCGA-AA-3518 HNRNPD SNP Missense_Mutation 4 83278485 T C 59 91 CRC TCGA-AA-3977 HNRNPD SNP Missense_Mutation 4 83279905 T G 64 77 UCEC TCGA-AP-A059 HNRNPD SNP Missense_Mutation 4 83278594 C T 30 98 UCEC TCGA-AX-A05Z HNRNPD SNP Silent 4 83278493 C A 32 64 KIRC TCGA-B8-4143 HNRNPD SNP Missense_Mutation 4 83280713 C T 17 99 BRCA TCGA-BH-A0B8 HNRNPD SNP Missense_Mutation 4 83277695 T C 49 91 UCEC TCGA-BS-A0UF HNRNPD SNP Silent 4 83278508 C A 32 64 HNSC TCGA-CV-7183 HNRNPD INS Frame_Shift_Ins 4 83280734 - C 3 91 UCEC TCGA-D1-A103 HNRNPD SNP Missense_Mutation 4 83277987 C T 32 99 BRCA TCGA-D8-A1XW HNRNPD DEL Frame_Shift_Del 4 83278494 TT - 56 91 UCEC TCGA-EO-A1Y5 HNRNPD DEL In_Frame_Del 4 83278008 TGCTGA - 63 90 BLCA TCGA-G2-A2ES HNRNPD SNP Missense_Mutation 4 83280703 G A 36 99