ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW38-PRE CCR7 SNP Nonsense_Mutation 17 38711066 C T 18 70 LUAD LUAD-B00731 CCR7 SNP Missense_Mutation 17 38711643 G A 45 83 MEL MEL-JWCI-WGS-23 CCR7 SNP Silent 17 38711324 G A 37 30 MEL MEL-UKRV-Mel-20 CCR7 SNP Missense_Mutation 17 38711011 T G 59 89 MEL MEL-UKRV-Mel-20 CCR7 SNP Silent 17 38711921 G A 37 50 LUSC TCGA-85-6561 CCR7 SNP Silent 17 38711930 G T 45 85 UCEC TCGA-A5-A0VP CCR7 SNP Missense_Mutation 17 38711130 C T 27 88 BRCA TCGA-A8-A09A CCR7 SNP Missense_Mutation 17 38711716 T A 54 91 CRC TCGA-AA-3681 CCR7 SNP Missense_Mutation 17 38711595 C A 17 74 CRC TCGA-AA-3977 CCR7 SNP Silent 17 38711921 G A 37 50 CRC TCGA-AG-3892 CCR7 SNP Missense_Mutation 17 38711971 G A 38 69 CRC TCGA-AG-A002 CCR7 SNP Missense_Mutation 17 38711994 G T 33 53 BRCA TCGA-AO-A124 CCR7 SNP Nonsense_Mutation 17 38711515 G A 46 56 UCEC TCGA-AP-A051 CCR7 SNP Missense_Mutation 17 38712013 C T 30 95 UCEC TCGA-AP-A054 CCR7 SNP Missense_Mutation 17 38711262 T C 60 52 UCEC TCGA-AP-A059 CCR7 SNP Missense_Mutation 17 38711266 C T 26 52 UCEC TCGA-AP-A0LM CCR7 SNP Silent 17 38711780 G A 38 47 UCEC TCGA-B5-A11Y CCR7 SNP Missense_Mutation 17 38711511 G A 38 61 UCEC TCGA-BK-A0C9 CCR7 INS Frame_Shift_Ins 17 38715169 - A 21 53 BLCA TCGA-BT-A0YX CCR7 SNP Silent 17 38711549 G C 41 70 HNSC TCGA-CV-7245 CCR7 SNP Missense_Mutation 17 38711638 G A 45 82 BRCA TCGA-D8-A1JG CCR7 SNP Missense_Mutation 17 38721654 A T 7 59 BLCA TCGA-G2-A2EO CCR7 SNP Missense_Mutation 17 38711414 C T 29 87 BLCA TCGA-GD-A3OP CCR7 DEL Frame_Shift_Del 17 38711926 AA - 5 76 HNSC TCGA-HD-7753 CCR7 SNP Silent 17 38711204 G A 40 35