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1. Duplication - Where a portion of a chromosome is duplicated, resulting in multiple copies of the region.

2. Deletions - When a deletion of a nucleotide (nitrogen bases of a DNA) causes a shift of the mRNA codons. This will cause Alternations of Amino Acids.

3. Insertions - Occurs when an extra nucleotide is added.

4. Inversions - When a portion of a chromosome breaks off and reinserts itself in the same spot but in the reversed position

5. Translocation - When a portion of 2 chromosomes break off and switch locations

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7mo ago

Some examples of mutations in chromosomes include deletion, duplication, inversion, and translocation. These mutations can lead to genetic disorders or changes in an individual's traits.

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  1. Chromosomal disorder
  2. Chromosome disorder
  3. Chromosomal abnormality
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Q: What are names of mutations in chromosomes?
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Related questions

Are chromosomes bad for mutations?

No. But they are necessary for mutations to arise. Likewise, they are also necessary in order for mutations not to arise.


Steps in meiosis that increase variability?

crossing over of chromosomes, indepependent segregation of chromosomes and mutations


Can somatic mutations occur in sex chromosomes?

Yes, somatic mutations can occur in sex chromosomes. These mutations can affect the genes located on the X or Y chromosome, leading to genetic changes in somatic cells, which are not passed on to offspring. Somatic mutations on sex chromosomes can impact an individual's health and development.


What does insertion and inversion mutation have in common?

They are both mutations of chromosomes


What are the types of chromosomes mutations?

Duplication, translocation, inversion, deletion.


Somatic mutations occur in sex chromosomes and can be inherited?

true


What Is a dominant disorder?

dominant disorder is caused by mutations in genes on the x chromosomes.


What are the three ways chromosomes can cause mutations?

point mutation, insertion and deletion


What is a karyotype and what type of mutation does it show?

A karyotype is a visual representation of an individual's chromosomes. It can show various types of mutations, such as deletions, duplications, translocations, and inversions, by displaying changes in the number or structure of chromosomes.


What causes a baby to come out deformed?

Mutations in their chromosomal DNA. Each parent gives chromosomes to the baby, and when they meet sometimes there are doubles of chromosomes, missing chromosomes, or mutated chromosomes which cause abnormalities in the DNA and overall the child.


What are the types of mutation?

There are a few mutations caused by entire chromosome changes. The times the number of chromosome can change can occur when the duplicated chromosomes pull apart and then produce a cell missing a chromosome or having an additional one. For example, XO or XXX or XXY. These are the sex chromosomes where XO means that either the second X is missing, or the Y is missing. Normal would be XX (female) or XY (male). These individuals are able to live with these added or deleted genes. All other missing or additional chromosomes are not compatible with life.


Describe four types of mutations resulting from the breakage of chromosomes?

Deletion, duplication, inversion, translocation.