AP BIOLOGY

THE MOLECULAR BASIS OF INHERITANCE

GENE MUTATION

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Identify the gene mutation:NormalAGC-TTA-CGT-AAAMutantACT-TAC-GTA-AA
A
insertion frameshift
B
deletion frameshift
C
insertion
D
nonsense
Explanation: 

Detailed explanation-1: -There are many genetic tests that require a sample of your blood, skin, hair, amniotic fluid or tissues to identify changes to your genes, chromosomes or proteins. Genetic testing can locate mutated genes or chromosomes that cause genetic conditions.

Detailed explanation-2: -Mutations can be of many types, such as substitution, deletion, insertion, and translocation.

Detailed explanation-3: -These hereditary (or inherited) mutations are in almost every cell of the person’s body throughout their life. Hereditary mutations include cystic fibrosis, hemophilia, and sickle cell disease.

Detailed explanation-4: -Deletion. Deletion mutations are actually the cause for a large number of genetic diseases, such as two-thirds of cystic fibrosis cases and the cat cry syndrome, which is so-called because children with this syndrome often have a cry that sounds similar to a cat meowing.

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