Chapter 11 Hardy Weinberg and Mutations Flashcards

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1
Q

A somatic cell mutation that results in under-expression of multiple genes

A) Chromosomal addition
B) Sex Chromosome Y-linked inversion
C) Autosomal dominant reversion
D) Sex Chromosome X-linked accumulation
E) Chromosome deletion
A

E

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2
Q

A de-novo (new) gamete-cell mutation has which of the following characteristics?

A) All offspring are affected
B) One parent must be a carrier
C) Both parents must be carriers
D) The condition cannot be transmitted to progeny
E) The condition must be transmitted to male progeny

A

c

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3
Q

Once a spontaneous dominant mutation has occurred in the progeny of a cross, it will become phenotypically evident at what time?

A) When the affected individual mates with a sibling
B) When the affected individual mates with a cousin
C) When the affected individual mates with another affected individual
D) Immediately
E) Never

A

D

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4
Q

Which of the following are required for a population to be in genetic equilibrium?

A) No Mutation
B) Survival of the Fittest
C) No Natural Selection
D) Migration
E) Random Mating
A

A
C
E

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5
Q

Worldwide, gene ABCD has an “R” amino acid in its polypeptide at position 64. The mutations p.R64T (53% of Asians), p.R64G (51% Europeans) mean which of the following could be relevant/true?

A) At least two different population based wild types
B) A substantial number of individuals with a mutation
C) Migration-based wild types
D) Founder-based mutation selection
E) All of the above

A

A

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6
Q

Identical twins were separated at birth. 27 years later, they found each other and were surprised that both of them were 5’ 8” tall. This is an example of:

A) Environmental influence
B) Natural selection
C) Heritability
D) Mutation selection
E) Reproductive success
A

c

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7
Q

The portion of a phenotype that is caused by the environment is considered to be…

A) Heritable
B) Transmittable
C) Migrational
D) Central
E) None of the above
A

E

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8
Q

Disease A is autosomal recessive. A total of 36% of the study population of 100 people are affected. How many homozygous unaffected individuals are in the study population?

A) 16
B) 24
C) 36
D) 48
E) 60
A

D

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9
Q

Disease A is autosomal recessive. A total of 36% of the study population of 100 people are affected. How many carriers are in the study population?

A) 16
B) 24
C) 36
D) 48
E) 60
A

C

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10
Q

The mutation p.Leu231Thr indicates what?

A) The coding sequence at DNA bp 231 has been changed to a Threonine in a sequence\
B) The amino sequence at DNA bp 231 has been changed to a Threonine in a sequence
C) The amino acid at position 231 has been changed to a Leucine in a polypeptide
D) The amino acid at position 231 has been changed to a Threonine in a polypeptide

A

D

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11
Q

Which of the following can cause mutation in Humans?

A) Ionizing Radiation
B) Microwaves
C) Mutagenic Chemicals
D) Transposable elements
E) Spider bites
A

A

C

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12
Q

Which of the following sequences would result from the annotation c.72dupTA​[3]? THINK CAREFULLY!

A) 5’ …AUCACUAUAUACAGAUA..3’
B) 5’ …ATCACTATACAGATA..3’
C) 3’ …ATCACTATACAGATA..5’
D) 5’ …ATCACTAATAATAACAGATA..3’
E) 5’ …ATCACTAUATTACAGAUA..3’
A

C

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13
Q

Which of the following conditions best describes this subjects OPA1 gene?

A) Hemizygous
B) Consanguineous
C) Heterozygous
D) Homozygous
E) All of the above
A

A

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