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A newborn's DNA Is screened for hearing loss. The codon sequence used as the check for normal hearing is TAT AGA GGA GGC MAG TOG TAA. However, the newborn's codon sequence comes back as TAT AGA GGA GAC
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A newborn's DNA Is screened for hearing loss. The codon sequence used as the check for normal hearing is TAT AGA GGA GGC MAG TOG TAA. However, the newborn's codon sequence comes back as TAT AGA GGA GAC AAG TCGTM

What can be concluded regarding the infant's codon sequence?

User Brett Daniel
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Answer: the codon sequence has a substitution mutation

Explanation: C

User Taco Jan Osinga
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