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Types of Changes in DNA
| Class of Mutation | Type of Mutation | Human Disease(s) Linked to This Mutation |
|---|---|---|
| Point mutation | Substitution | Sickle-cell anemia |
| Insertion | One form of beta-thalassemia | |
| Deletion | Cystic fibrosis | |
| Chromosomal mutation | Inversion | Opitz-Kaveggia syndrome |
- What are the 4 types of mutation?
- What are the 6 types of mutations?
- What are the 3 types of mutations?
- What is mutation example?
What are the 4 types of mutation?
Summary
- Germline mutations occur in gametes. Somatic mutations occur in other body cells.
- Chromosomal alterations are mutations that change chromosome structure.
- Point mutations change a single nucleotide.
- Frameshift mutations are additions or deletions of nucleotides that cause a shift in the reading frame.
What are the 6 types of mutations?
What kinds of gene variants are possible?
- Missense. A missense variant is a type of substitution in which the nucleotide change results in the replacement of one protein building block (amino acid) with another in the protein made from the gene. ...
- Nonsense. ...
- Insertion. ...
- Deletion. ...
- Duplication. ...
- Frameshift. ...
- Repeat expansion.
What are the 3 types of mutations?
There are three types of DNA Mutations: base substitutions, deletions and insertions.
- Base Substitutions. Single base substitutions are called point mutations, recall the point mutation Glu -----> Val which causes sickle-cell disease.
- Deletions. ...
- Insertions.
What is mutation example?
Other common mutation examples in humans are Angelman syndrome, Canavan disease, color blindness, cri-du-chat syndrome, cystic fibrosis, Down syndrome, Duchenne muscular dystrophy, haemochromatosis, haemophilia, Klinefelter syndrome, phenylketonuria, Prader–Willi syndrome, Tay–Sachs disease, and Turner syndrome.
