Essay
Any two human beings typically have an estimated 0.1% difference in their nucleotide sequences, which is equivalent to about 3 million nucleotide differences.These differences are the basis of the SNPs used to construct genetic linkage maps.Some of these SNPs actually lie in the region of the DNA that codes for the protein, yet they have no effect on the phenotype of individuals carrying the SNP on both homologous chromosomes.Explain how some SNPs can lie within the portion of the DNA that codes for the protein and yet have no discernible effect on the protein's activity.
Correct Answer:

Verified
Because of the redundancy of the genetic...View Answer
Unlock this answer now
Get Access to more Verified Answers free of charge
Correct Answer:
Verified
View Answer
Unlock this answer now
Get Access to more Verified Answers free of charge
Q13: You examine a worm that has two
Q14: Which of the following statements about conditional
Q15: Which of the following statements is TRUE?<br>A)Another
Q16: Which of the following does not describe
Q17: Which of the following statements most correctly
Q19: With respect to gene E on the
Q20: The single-nucleotide polymorphisms found in the human
Q21: Figure 19-27 is a diagram of chromosomes
Q22: During fertilization in humans,<br>A)a wave of Ca<sup>2</sup><sup>+</sup>
Q23: Meiosis includes a recombination checkpoint that is