One ma be born with physical, and or mental illness. Such as fragile X syndrome.
No
Any change in the sequence of DNA nucleotides is called mutation.
The specific expressed sequence of DNA that codes for a protein in this genetic sequence is called a gene.
Yes, a point mutation can cause a change in one single nucleotide in a DNA sequence.
The correct sequence of events for a mutation to affect the traits expressed by a cell is as follows: first, the mutation changes the DNA sequence of a gene. Next, this altered DNA is transcribed into messenger RNA (mRNA). Then, the mRNA is translated into a protein. Finally, the change in the protein can lead to a modified phenotype or trait expressed by the cell.
A mutation is a permenent in DNA sequence of a gene,mutation in a gene's DNA sequence can alterthe aminoacid sequence of the protein encodedby the gene.
One ma be born with physical, and or mental illness. Such as fragile X syndrome.
No
a change in the DNA sequence is a mutation, so I'm not sure what you're asking
A frameshift mutation occurs when nucleotides are inserted or deleted from a DNA sequence, shifting the reading frame of the gene. Given the original sequence AUGCCCACCCGA, a potential mutated sequence could be AUGCCCA---CCGA, where a nucleotide has been deleted, resulting in a shift. Without specific options to choose from, it's essential to identify a sequence that deviates from the original by an insertion or deletion that disrupts the reading frame.
Missence mutation
State diagram represents behavior without noting the classes involved whereas sequence diagram represents behavior, by describing how classes move from state to state
Any change in the sequence of DNA nucleotides is called mutation.
When a mutation occurs outside a gene, it is referred to as a "regulatory mutation" or "non-coding mutation." These mutations can affect gene expression by altering regulatory elements such as promoters, enhancers, or silencers, which control when and how much a gene is expressed. Although they do not change the protein-coding sequence, they can still have significant effects on an organism's phenotype.
A frameshift mutation is caused by adding one nucleotide into the middle of a sequence. This type of mutation alters the reading frame of the genetic code, leading to a completely different amino acid sequence downstream of the insertion point.
The original DNA sequence is AGC CCG TA. Inserting the mutation yields AGC CTT GGC AT. This mutation results in a substitution of a single nucleotide in the original sequence.