A tool to identify, extract and map point mutations from literature on the protein reported. It uses a protein sequence or a multiple sequence alignment in fasta format as input. It uses a Uniprot ID or an Accession code provided as a descriptor to retrieve protein information from Uniprot. From there, it extracts protein names, gene names and synonyms. These are used as keywords to download abstracts. The retrieved abstracts are scanned for mutations. Mutations reported are mapped onto the amino acid sequence.