The complementary sequence of this DNA molecule:

What is CGCATG?
The two steps in building a protein.

What are transcription (Step A) and translation (Step B)?
This number of nucleotides makes a codon.
What is three?
The probability of seeing a recessive trait when two heterozygotes mate.
What is 25%?
The type of mutation shown.

What is a substitution mutation?
The two complementary base pairs of DNA.
What is A pairs with T and C pairs with G?
OR
What adenine pairs with thymine and cytosine pairs with guanine?
Identify the cellular locations.

What are
Location 1 - nucleus
Location 2 - cytoplasm
Location 3 - ribosome
?
The two codons that code for Leu.

What are UUA and UUG?
The types of dominance shown.

What are
Type A - incomplete dominance
Type B - codominance
?
This type of mutation has no effect on the protein because it codes for the same amino acid as the original sequence.

What is a silent mutation?
Structure 2.

What is a nucleotide?
Sections of DNA that code for proteins.
What are genes?

The process shown here.

What is transcription?
This is the genotype of Individual 1. Use the pedigree shown:

What is Aa (heterozygous)?
Cells are shown in meiosis. Which cell could result in a trisomy?

What is Cell B?
These bonds hold together base pairs. Labeled here as X.

What are hydrogen bonds?
In RNA, this base replaces thymine.
What is uracil?
OR
What is U?
Proteins are made from these building blocks.
What are amino acids?
What is a 100% chance?
Because this type of mutation changes the reading frame of a gene, it is usually detrimental to the final protein product.
What is a frameshift mutation?

The two components that makeup the backbone of the DNA double helix. Outlined here in red.

What are sugars and phosphates?
The amino acids coded for by this DNA sequence: TCA TGC

What is Ser - Thr ?
How did you get that?
First transcribe DNA to mRNA = AGU ACG
Then, use the codon chart
AGU = Ser
ACG = Thr
Structures A, B and C.

What are tRNA, ribosome, mRNA?
Color blindness is an X-linked recessive trait. This is the probability that a female will be colorblind if the mom is a carrier for color blindness and the dad has normal vision.
What is a 0% chance?

These two words describe the mutation shown.
One word is for the gene change, one word is for the amino acid change.

What are substitution mutation AND nonsense mutation?
