ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0167 HLCS SNP Missense_Mutation 21 38302656 A T 13 41 HNSC HN_62532 HLCS SNP Missense 21 38132135 T C 60 74 LUAD LUAD-FH5PJ HLCS SNP Missense_Mutation 21 38269392 C T 17 55 LUAD TCGA-05-4249 HLCS SNP Silent 21 38137445 A G 7 49 OV TCGA-09-2044 HLCS SNP Missense_Mutation 21 38309277 G T 44 64 OV TCGA-13-0755 HLCS SNP Missense_Mutation 21 38309497 C T 20 51 LUSC TCGA-22-4613 HLCS SNP Missense_Mutation 21 38309018 C G 18 58 LUSC TCGA-34-2600 HLCS SNP Missense_Mutation 21 38309032 G A 33 63 LUSC TCGA-34-5231 HLCS SNP Missense_Mutation 21 38137351 C A 26 94 LUSC TCGA-39-5036 HLCS SNP Splice_Site 21 38311131 C T 17 90 LUSC TCGA-60-2720 HLCS SNP Missense_Mutation 21 38309503 G C 33 61 LUSC TCGA-66-2758 HLCS SNP Silent 21 38309157 A T 9 33 CRC TCGA-AA-3811 HLCS SNP Silent 21 38308962 A G 6 43 CRC TCGA-AA-3966 HLCS SNP Nonsense_Mutation 21 38302697 G A 46 63 CRC TCGA-AA-3977 HLCS SNP Missense_Mutation 21 38302646 C T 31 64 CRC TCGA-AA-3984 HLCS SNP Missense_Mutation 21 38302646 C T 31 64 CRC TCGA-AA-A022 HLCS SNP Missense_Mutation 21 38309369 C T 31 98 CRC TCGA-AG-3878 HLCS SNP Missense_Mutation 21 38269293 C T 18 50 CRC TCGA-AG-A002 HLCS SNP Missense_Mutation 21 38302646 C T 31 64 CRC TCGA-AG-A025 HLCS SNP Silent 21 38309487 A G 7 39 UCEC TCGA-AP-A051 HLCS SNP Silent 21 38269246 G T 33 49 UCEC TCGA-AP-A056 HLCS SNP Silent 21 38302554 C T 23 13 UCEC TCGA-B5-A11E HLCS SNP Missense_Mutation 21 38302694 T G 60 52 UCEC TCGA-B5-A11E HLCS SNP Missense_Mutation 21 38309057 A G 14 43 UCEC TCGA-B5-A11E HLCS SNP Missense_Mutation 21 38309482 T C 58 51 UCEC TCGA-BG-A2AE HLCS SNP Silent 21 38139568 C T 27 36 BRCA TCGA-BH-A0W4 HLCS SNP Missense_Mutation 21 38308910 C T 31 53 UCEC TCGA-BS-A0UJ HLCS SNP Missense_Mutation 21 38309383 T C 56 46 UCEC TCGA-BS-A0UV HLCS SNP Splice_Site 21 38302735 T C 55 83 HNSC TCGA-CV-5435 HLCS SNP Missense_Mutation 21 38308946 C T 20 62 UCEC TCGA-D1-A167 HLCS SNP Missense_Mutation 21 38269365 C T 23 51 BLCA TCGA-DK-A1AG HLCS SNP Missense_Mutation 21 38126600 C T 30 96 BLCA TCGA-DK-A2I4 HLCS SNP Silent 21 38126565 G A 41 48 BLCA TCGA-DK-A2I4 HLCS SNP Missense_Mutation 21 38309074 G C 41 98 BLCA TCGA-DK-A3IT HLCS SNP Missense_Mutation 21 38126702 G C 33 83