The tool identifies mutations listed by NCBI, after analyzing SARS-CoV-2 SRA Data. Reference
Indels are not analyzed. Check for updates!
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.