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12U3 L9 mutations

Total questions: 10

Worksheet time: 9mins

Name
Class
Date
1.

What is a mutation?

a)

A change in a DNA base sequence

b)

A change in an RNA codon sequence

c)

A change in an amino acid sequence

d)

A change in the tertiary shape of a protein

2.

What type of mutation involves one base being exchanged for another?

a)

Substitution

b)

Deletion

c)

Insertion

d)

Frame shift

3.

Which of the following shows a substitution mutation during replication of the sequence AAT GCC AGA?

a)

TTA CCG TCT

b)

TTA CGG TCT

c)

TTA CGG TC

d)

TTA CGG TTC T

4.

A substitution mutation occurs on the DNA sequence AGG, changing the triplet to AGA. What effect does this have on the final protein?

a)

No effect, both triplets code for serine

b)

No effect, both triplets code for arginine

c)

The protein will contain arginine instead of serine

d)

The protein will contain serine instead of arginine

5.

Why are substitution mutations least likely to have an effect on the final protein?

a)

Because different codons can encode the same amino acid

b)

Because different codons encode different amino acids

c)

Because each amino acid has its own unique codon

d)

Because the genetic code is universal

6.

Which type(s) of mutations cause frame-shift?

a)

Deletion

b)

Insertion

c)

Substitution

d)

Point

7.

What is frame-shift?

a)

When every codon that follows a mutation is altered

b)

When a single codon is altered by a mutation

c)

When a mutation affects the sequence of amino acids in a protein

d)

When a mutation affected the final tertiary structure of a protein

8.

What is not an effect of a mis-sense mutation?

a)

A codon encodes a different amino acid

b)

A codon becomes a stop codon and does not encode an amino acid

c)

One or more of the bases in a codon is altered

d)

All subsequent codon sequences are altered (frame shift)

9.

What is the term used to describe a substitution mutation that turns a coding sequence into a stop codon?

(a)  

10.

A substitution mutation occurs on the DNA sequence that changes the mRNA codon CCG to CGG. How can this mutation be described?

a)

Mis-sense

b)

Non-sense

c)

Silent