A specific single nucleotide variant in the human genome occurs with a 5% frequency in the general population. This variant occurs within the protein coding region but does not change the encoded protein sequence. Which one of the following best described this variance?   Question 25 options:   Synonymous coding single nucleotide polymorphism   Non-coding single nucleotide polymorphism   Nonsynonymous coding single nucleotide polymorphism   Missense point mutation   Sense point mutation

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