Answer:
mRNA: 3' AUG-AAU-GCU-GCC-GGU-GA-5'
amino acids : methionine, asparagine, alanine, arginine, proline
type of mutation: deletion, missense
Explanation:
The mRNA sequence is complementary to the DNA sequence. A always pairs with T, C always pairs with G. Except this is an RNA sequence not a DNA sequence, so T is replaced with U.
The mRNA sequence is translated into an amino acid sequence based on the triplet code. The triplet code for this sequence is shown in the attached picture. Each triplet signifies a specific amino acid. The codon can be identified from the table and placed in sequence. We can see that the new DNA strand has caused a new amino acid sequence. It has also left us with an incomplete sequence, as GA cannot signify an amino acid.
The type of mutation is a single base deletion. We can see that the base C is missing from the 9th amino acid in the original strand. As you can see, this has an ongoing affect on all the bases in the rest of the sequence, as it changes the way the sequence is organised into codons. This results in a missense mutation.
Answer:
Earth's climate has gotten consistently warmer over time.
Answer:
C.emigration is the answer......
A comet always points in the opposite direction of the comet hence why it’s called the tail
Ansa million. once you're staring at in ordinary terms one technology, it relatively is, all those fruit flies have been produced via 2 mum and dad, then the only plausible parental genotype that provide you a 50/50 ratio is that if the mummy is XwXw and the father is Xry... this gene is carried on the X chromosome, and w represents white eyes and r represents purple eyes. you are able to bypass forward and draw this out in case you like, even yet it provides 50% heterozygous women individuals (with purple eyes, provided that purple is dominant), and 50% white eyed men, who can in ordinary terms inherit Xw from their mom. The Y that they could inherit from the father could have not any effect on their eye shade. it relatively is comparable for women individuals, they are in a position to in ordinary terms inherit Xw from their mom and an Xr from their father, meaning they'll continually be heterozygous for the attention shade gene. 2. returned, set us the genotypes so which you will visualize it; we are going to say that this disease is carried on the X chrmsm (thats whats usually assumed), and the gene for customary creative and prescient is XB, yet for colorblindness its Xb. those are dominant/recessive to boot. So, if the girl is a provider, her genotype is XBXb, and if the male is colorblind, his genotype is XbY. in case you draw this out in a punett sq., you will get 25% heterozygous woman, 25% colorblind woman, 25% well-known male, and 25% colorblind male. so, there's a 50% risk that any baby they have would be colorblind, 50% risk if its a woman, or 50% risk if it relatively is male.wer:
Explanation:
