ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62739 RYK SNP Missense 3 133896892 A G 6 89 OV TCGA-10-0937 RYK SNP Synonymous 3 133896881 T C 56 57 OV TCGA-24-1104 RYK SNP Missense_Mutation 3 133907752 A G 4 88 OV TCGA-61-2012 RYK SNP Missense_Mutation 3 133907756 G A 38 73 CRC TCGA-AA-3821 RYK SNP Missense_Mutation 3 133878104 C A 28 63 CRC TCGA-AA-3977 RYK SNP Silent 3 133894820 C T 26 73 CRC TCGA-AA-3977 RYK SNP Missense_Mutation 3 133907709 T G 64 62 CRC TCGA-AG-A002 RYK SNP Missense_Mutation 3 133878114 C T 31 100 CRC TCGA-AG-A002 RYK SNP Silent 3 133894834 C A 30 99 UCEC TCGA-AP-A0LM RYK SNP Missense_Mutation 3 133878114 C T 31 100 UCEC TCGA-AX-A063 RYK SNP Silent 3 133930412 C T 26 95 UCEC TCGA-B5-A0JY RYK SNP Missense_Mutation 3 133896873 T G 56 89 UCEC TCGA-B5-A0JY RYK SNP Missense_Mutation 3 133907683 T C 64 88 UCEC TCGA-BS-A0UV RYK SNP Splice_Site 3 133896918 C A 32 97 UCEC TCGA-BS-A0UV RYK SNP Silent 3 133907742 C T 30 53 UCEC TCGA-BS-A0UV RYK SNP Silent 3 133941271 C T 31 46 UCEC TCGA-D1-A17Q RYK SNP Silent 3 133926324 C A 32 71