Please help!

Parent 1 doesn't have freckles, but his parents did. Parent 2 has freckles, all of parent 2 family has freckles as well. Use the letters provided in the Punnett square to answer the following questions:

What is the genotype of parent 1?

What is the genotype of parent 2?

What is the probability that the offspring of parent 1 and parent 2 has the recessive alleles be expressed in their phenotype? __% (use numbers only)

Answers

Answer 1

Answer:

denoting No freckles: N Freckles: f,

parent 1 genotype: Nf

parent 2 genotype: ff

after using punnet Square the four random combinations are:

Nf, Nf, ff, ff

50% probability that offspring will have freckles

Answer 2

Answer: Genotype of parent 1: Aa

Genotype of parent 2: aa

Probability: 50%

Explanation: The Punnet square is shown in the problem to help you :) Also, these answers are correct because I got these all right on my science quiz just recently!


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Justifying Conclusions
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article you just read.
Is the conclusion justified by the evidence?
✓yes
COMPLETE
What, if anything, is missing from the article
that would help you to evaluate whether the
conclusion is justified?
Intro
4 of 5
D

Answers

Answer:

1 chech data for errs

2 consider issues of context wjen interpreting data

3 Access results againstavailable literature

4 compare different method for consistency in findings

5 consider alternative explanations

Answer:

yes

Explanation:

decide whether the following statement is true or false, and then explain why: "in an organism whose genome has been sequenced, identifying the mutant gene responsible for an interesting phenotype is as easy for mutations induced by chemical mutagenesis as it is for those generated by insertional mutagenesis"

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FALSE

This is false because when the genome is sequenced for a particular organism, it is easy to compare the sequence with the reference and check if there is any mutation that has led to change in phenotype. The chemical mutagenesis is basically change of one base pair at a time and hence it is easy to sequence and find out which base pair has changed leading to the mutagenesis. However, when it comes to insertional mutagenesis, this occurs using either T-DNA or transposons and it is caused by viruses or transposons which leads to creation of such mutations. The TE (transposable elements) are DNA sequences which move from one location to another within a genome and hence when mutations take place due to this, it becomes difficult to compare it with the reference to identify the mutations.

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