ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0060 CCT2 SNP Missense_Mutation 12 69991825 G C 41 97 MEL ME009 CCT2 SNP Missense_Mutation 12 69981312 G A 33 83 MEL MEL-JWCI-WGS-1 CCT2 SNP Missense_Mutation 12 69983284 C T 23 83 LUAD TCGA-05-4249 CCT2 SNP Missense_Mutation 12 69983267 C T 30 77 LUAD TCGA-05-4396 CCT2 SNP Nonsense_Mutation 12 69980089 G T 35 94 GBM TCGA-06-2565 CCT2 SNP Missense_Mutation 12 69987309 C T 30 100 GBM TCGA-12-5295 CCT2 SNP Silent 12 69985894 T G 53 46 LUAD TCGA-44-6777 CCT2 SNP Splice_site 12 69991418 G T 44 98 LUAD TCGA-49-4486 CCT2 SNP Silent 12 69993722 G C 45 70 CRC TCGA-AG-A002 CCT2 SNP Missense_Mutation 12 69991759 A C 12 86 UCEC TCGA-AP-A051 CCT2 SNP Nonsense_Mutation 12 69985880 C T 19 54 UCEC TCGA-AP-A051 CCT2 SNP Missense_Mutation 12 69993775 C T 27 99 UCEC TCGA-AP-A056 CCT2 SNP Silent 12 69981762 C T 23 57 UCEC TCGA-AP-A05A CCT2 SNP Missense_Mutation 12 69990984 G A 41 83 UCEC TCGA-AX-A0J0 CCT2 SNP Silent 12 69981998 G A 37 55 UCEC TCGA-AX-A0J0 CCT2 SNP Silent 12 69986773 A G 13 50 UCEC TCGA-B5-A11J CCT2 SNP Silent 12 69992134 T C 51 57 UCEC TCGA-B5-A11Y CCT2 SNP Missense_Mutation 12 69991840 G T 34 97 HNSC TCGA-BA-6868 CCT2 SNP Missense_Mutation 12 69986801 G C 33 82 BRCA TCGA-BH-A0EE CCT2 SNP Missense_Mutation 12 69981336 G C 45 97 BRCA TCGA-BH-A18T CCT2 SNP Missense_Mutation 12 69991764 G C 45 80 UCEC TCGA-BS-A0UF CCT2 SNP Missense_Mutation 12 69985881 G A 37 80 UCEC TCGA-BS-A0UF CCT2 SNP Nonsense_Mutation 12 69991468 G T 45 78 UCEC TCGA-BS-A0UV CCT2 SNP Missense_Mutation 12 69983347 G T 33 83 HNSC TCGA-CV-7089 CCT2 SNP Missense_Mutation 12 69987352 A T 8 91 KIRC TCGA-CZ-4866 CCT2 SNP Silent 12 69985846 G T 48 52 UCEC TCGA-D1-A174 CCT2 SNP Missense_Mutation 12 69981367 T C 60 76 UCEC TCGA-D1-A17A CCT2 SNP Silent 12 69980553 C T 31 49 UCEC TCGA-D1-A17Q CCT2 SNP Missense_Mutation 12 69986847 G A 40 82