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This library is faily specific for my own purposes. It's on crates.io so that Ican pull it as a dependency for my project. The code is mature at this point.But it could really use some more doc comments.

This library reads genomic sequences of transcripts and mutates everynucleotide in that transcript to determine how many mutations of a type(synonymous, missense, nonsense, ...) can be generated and what theirprobabilities are. This is useful to when you try to identify disease genes bycomparing mutated genes across affected individuals and you need to determinehow many mutations you can expect by chance.