ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0030 HYAL1 SNP Missense_Mutation 3 50339816 C T 23 44 BRCA BR-MEX-191 HYAL1 SNP Silent 3 50337926 C T 32 47 MEL MEL-JWCI-WGS-23 HYAL1 SNP Missense_Mutation 3 50340318 C T 22 63 MEL MEL-Ma-Mel-37 HYAL1 SNP Missense_Mutation 3 50338140 G A 42 61 PRAD PR-05-3595 HYAL1 DNP Missense_Mutation 3 50339882 GC TT 46 49 LUAD TCGA-05-4396 HYAL1 SNP Missense_Mutation 3 50339933 C A 23 52 LUSC TCGA-18-3406 HYAL1 SNP Nonsense_Mutation 3 50338437 C T 22 63 LUSC TCGA-22-4601 HYAL1 SNP Splice_site 3 50340387 T C 51 50 LUSC TCGA-37-4135 HYAL1 SNP Missense_Mutation 3 50339528 A T 10 56 UCEC TCGA-A5-A0GM HYAL1 SNP Missense_Mutation 3 50339817 G A 38 44 CRC TCGA-AA-A01R HYAL1 SNP Silent 3 50338046 C T 27 27 UCEC TCGA-AP-A0LM HYAL1 SNP Missense_Mutation 3 50339751 G T 33 46 UCEC TCGA-B5-A11E HYAL1 SNP Missense_Mutation 3 50339994 C T 26 59 KIRC TCGA-CJ-4873 HYAL1 SNP Missense_Mutation 3 50338003 C T 29 55 HNSC TCGA-CV-5439 HYAL1 SNP Missense_Mutation 3 50338477 G A 38 58 BLCA TCGA-G2-A3IE HYAL1 SNP Silent 3 50340340 G T 37 37