Classify Mutations Which Are Found Ny Using Exome Sequencing

Hi, everyone. I used exome sequencing to sequence tumor and blood, and after I remove mutations in blood and snp in dbsnp131, I found I still have about 2000 mutations. I read the exome sequencing paper, many of which classify mutations to synonymous mutations，missense mutations，nonsense mutations，splice-site changes，indel. But now I only have SNV and indel, I do not know which soft could I use to classify SNV to mutations，missense mutations，nonsense mutations，splice-site changes, looking forward to your answer, Thanks.