A cell membrane. Cell membranes are phospholipid bilayers (a.k.a 2 layers of phospholipids)
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
Answer: Mutation
Explanation: Mutation is a change in DNA sequence, it may occur due to error when the DNA is copied or it can arise from various environmental factors such as exposure to chemicals, UV radiation, Highly infectious microbes.
Mutation maybe spontaneous. Acquired mutations occur at some point in a person's life and are present only in certain cells, not in every cell in the body while some may target a tissue, an organ or an entire system.
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