Please solve this bioinformatics question: Read and analyze the following information: In a well-known human gene, a newly discovered variant has been reported. The full nucleotide sequence of this gene is available, as well as the nucleotide sequence which carries the newly discovered variation. This variation involves a change in 12 nucleotides. It is not a deletion or an insertion. It is a change in the nucleotide sequence but the specific 12 nucleotides which are consequent. Design a bioinformatics approach to investigate what structural and functional consequences would result from this variation. Consider all possible biological outcomes of this variation. Explain your bioinformatics research design step-by-step. Detail your approach and name all the software/databases you would use.

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