I am pretty sure the answer is c
The number of bases is no longer divisible by three. This results in a frame-shift, and all codons from the point of mutation will be affected.
Answer:
0.033
Explanation:
Tay–Sachs disease is an autosomal recessive disorder. The possible genotypes and phenotypes are:
- TT = normal
- Tt = carrier
- tt = Tay-Sachs disease
I will use <em>p </em>to call the frequency of the dominant <em>T</em> allele, and <em>q</em> the frequency of the recessive <em>t</em> allele.
If the population is in equilibrium, the frequency of the tt genotype is q².

The frequency of the Tt genotype is 2pq.

The Tay–Sachs carrier frequency will be 0.033
Divergent, convergent, and transform plate boundaries.
It is found in the X chromosome