The tool identifies mutations listed by NCBI, after analyzing SARS-CoV-2 SRA Data. Reference Indels are not analyzed. Check for updates! User Guide: 1. Input sequence has to be a complete genome sequence in fasta format.The input file can have multiple sequences in it. 2. Only mutations listed by NCBI are recognized based on nucleotides found in a particular position. 3. The variants are listed according to the mutations put by CDC. | |