ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MM MM-0468 CHIC2 SNP Missense_Mutation 4 54880013 C T 29 98 LUSC TCGA-46-3769 CHIC2 SNP Missense_Mutation 4 54930367 C A 26 92 CRC TCGA-AA-A010 CHIC2 SNP Missense_Mutation 4 54876267 C A 32 97 AML TCGA-AB-2922 CHIC2 SNP Missense_Mutation 4 54880243 C T 24 97 UCEC TCGA-AP-A051 CHIC2 SNP Missense_Mutation 4 54915202 G A 40 84 UCEC TCGA-AP-A054 CHIC2 SNP Splice_Site 4 54880228 A G 6 89 UCEC TCGA-AX-A05Y CHIC2 INS Frame_Shift_Ins 4 54880236 - TATA 44 74 UCEC TCGA-AX-A0J0 CHIC2 SNP Missense_Mutation 4 54915446 G T 33 97 UCEC TCGA-AX-A0J0 CHIC2 SNP Silent 4 54930447 G T 33 54 UCEC TCGA-B5-A0JY CHIC2 SNP Silent 4 54930447 G T 33 54 BRCA TCGA-BH-A204 CHIC2 SNP Missense_Mutation 4 54880282 C T 31 72 HNSC TCGA-CN-6019 CHIC2 SNP Missense_Mutation 4 54915177 C A 17 98 HNSC TCGA-CV-6936 CHIC2 SNP Missense_Mutation 4 54880271 C T 29 97 BRCA TCGA-D8-A1JK CHIC2 SNP Missense_Mutation 4 54930430 T G 58 84