ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME044 PRPH2 SNP Missense_Mutation 6 42666149 C T 30 87 MEL MEL-JWCI-WGS-13 PRPH2 SNP Silent 6 42666051 C T 24 80 MEL MEL-Ma-Mel-94 PRPH2 SNP Missense_Mutation 6 42689706 G A 37 56 OV TCGA-04-1356 PRPH2 SNP Missense_Mutation 6 42689611 C G 32 63 OV TCGA-04-1361 PRPH2 SNP Missense_Mutation 6 42690019 T A 56 49 GBM TCGA-06-0188 PRPH2 SNP Silent 6 42672106 G A 37 40 OV TCGA-13-0920 PRPH2 SNP Missense_Mutation 6 42672306 C T 19 99 LUAD TCGA-17-Z008 PRPH2 SNP Missense_Mutation 6 42689526 G A 37 75 OV TCGA-20-0990 PRPH2 SNP Missense_Mutation 6 42689522 T C 57 93 LUAD TCGA-35-5375 PRPH2 SNP Silent 6 42689590 G T 37 43 CRC TCGA-AA-3516 PRPH2 SNP Missense_Mutation 6 42689604 C T 31 100 CRC TCGA-AA-3715 PRPH2 SNP Silent 6 42672325 C T 26 48 CRC TCGA-AA-3947 PRPH2 SNP Missense_Mutation 6 42690068 G A 38 84 CRC TCGA-AA-3977 PRPH2 SNP Missense_Mutation 6 42689525 C T 27 100 CRC TCGA-AA-A02O PRPH2 SNP Missense_Mutation 6 42689706 G A 37 56 AML TCGA-AB-2828 PRPH2 SNP Silent 6 42690049 A G 5 49 CRC TCGA-AG-A01L PRPH2 SNP Silent 6 42689824 G A 40 45 UCEC TCGA-AP-A056 PRPH2 SNP Missense_Mutation 6 42689589 C T 31 88 UCEC TCGA-AP-A056 PRPH2 SNP Missense_Mutation 6 42689604 C T 31 100 UCEC TCGA-AX-A05Z PRPH2 SNP Missense_Mutation 6 42672347 C T 31 99 KIRC TCGA-B0-4694 PRPH2 SNP Missense_Mutation 6 42690020 T C 63 89 KIRC TCGA-B0-5698 PRPH2 SNP Missense_Mutation 6 42666085 T C 60 60 UCEC TCGA-B5-A0JY PRPH2 SNP Missense_Mutation 6 42689995 G T 33 48 UCEC TCGA-B5-A11E PRPH2 SNP Missense_Mutation 6 42666223 C T 27 75 UCEC TCGA-B5-A11E PRPH2 SNP Missense_Mutation 6 42666236 T G 57 66 UCEC TCGA-B5-A11N PRPH2 SNP Missense_Mutation 6 42689936 C T 31 63 UCEC TCGA-BS-A0UV PRPH2 SNP Silent 6 42672277 C T 27 35 BLCA TCGA-BT-A20O PRPH2 SNP Silent 6 42672298 G A 45 77 BLCA TCGA-BT-A3PH PRPH2 SNP Missense_Mutation 6 42689881 C G 29 63 HNSC TCGA-CN-6020 PRPH2 SNP Silent 6 42689520 G A 35 79 HNSC TCGA-CR-7385 PRPH2 SNP Silent 6 42689524 G A 34 58 HNSC TCGA-CV-7427 PRPH2 SNP Missense_Mutation 6 42666224 G A 38 83 HNSC TCGA-CX-7086 PRPH2 INS Frame_Shift_Ins 6 42666201 - T 8 48 HNSC TCGA-D6-6516 PRPH2 SNP Missense_Mutation 6 42689888 T C 60 90