The ΔF508 human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence, causing the loss of the amino acid phenylalanine located at position 508.
Source
Oak Ridge National Laboratory, Human Genome Project website
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|Description=The [[ΔF508]] [[human genome]] [[mutation]] is characterized by the deletion of three [[base pairs]] in the [[CFTR]] [[nucleotide sequence]], causing the loss of the [[amino acid]] [[phenylalanine]] located at position 508.
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