| Keyword | CPC | PCC | Volume | Score |
|---|---|---|---|---|
| example of a missense mutation | 0.01 | 1 | 8262 | 42 |
| example of conservative missense mutation | 1.54 | 0.5 | 350 | 18 |
| missense mutation disease example | 1.95 | 0.2 | 540 | 56 |
| example of missense mutation in a sequence | 1.44 | 0.5 | 5231 | 8 |
| what is an example of a missense mutation | 1.77 | 0.5 | 3268 | 81 |
| non conservative missense mutation | 1.72 | 0.4 | 2466 | 34 |
| example of missense mutation | 1.4 | 1 | 2318 | 62 |
| examples of missense mutation | 0.7 | 1 | 8320 | 94 |
| give an example of a missense mutation | 1.97 | 0.3 | 6692 | 49 |
| types of missense mutation | 1.24 | 0.6 | 118 | 1 |
| conservative and non conservative mutations | 1.82 | 0.9 | 9229 | 67 |
| what is a conservative mutation | 1.09 | 0.4 | 183 | 44 |
| types of mutations missense nonsense | 1.17 | 0.4 | 632 | 18 |
| missense mutation and nonsense mutation | 1.94 | 1 | 6733 | 72 |
| missense mutation nonsense mutation | 1.78 | 1 | 248 | 71 |
| types of mutations missense | 0.56 | 0.8 | 3558 | 67 |
| missense and nonsense mutation | 1.68 | 0.7 | 2123 | 75 |
| in a missense mutation | 0.11 | 0.4 | 7951 | 95 |
| nonsense and missense mutations | 0.19 | 0.1 | 2373 | 33 |
| what are missense mutations | 1.41 | 0.9 | 3014 | 79 |
What are the four types of genetic mutations? The four main types of chromosomal mutations are deletion, duplication, inversion and translocation. A fifth chromosomal mutation is known as a deficiency. This occurs when a chromosome is lost sometime during fertilization or development of a fetus.
What does missense mutation mean and how is it caused?The missense mutation which causes all of this is the difference of one nucleotide. It is first translated into mRNA, then into a protein. The missense mutation causes a valine to be placed where a glutamic acid normally goes. This non-conservative missense mutation causes the shape of the protein, hemoglobin, to change.
What does a missense mutation look like?Nonsense Mutation A nonsense mutation is the substitution of a single base pair that leads to the appearance of a stop codon where previously there was a codon specifying an amino acid. The presence of this premature stop codon results in the production of a shortened, and likely nonfunctional, protein.
