Performing a cut (also known as earthmoving)
<span>rocks undergo this when stress builds up past a certain point, called the ... is any fracture or system of fracture or system of fractures along which earth ... the fracture is caused by horizontal shear and movement is mainly horizontal </span><span>many kind of rocks that make up Earth's crust fail when stress is applied too quickly ... The resulting fracture or system of fractures along which movement occurs.</span>
Answer:
Rex is not a Tyrannosaurus rex because each of his hands has three fingers. Tyrannosaurus had only two fingers on each hand.
Answer:
The answer is C. Species diversity or B. Ecosystem diversity everyone thinks it either those 2 nobody really knows.
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
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