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Is translocation a type of mutation?

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Anonymous

13y ago
Updated: 4/23/2023

chromosomal mutation

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Alvah Stokes

Lvl 13
2y ago

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Related Questions

A mutation caused by a piece of DNA breaking away from its chromosome and becoming attached to a nonhomologous chromosome is called?

This type of mutation is called a translocation mutation. It involves the movement of a segment of DNA from one chromosome to another non-homologous chromosome, leading to potential genetic changes and abnormalities.


What is reciprocal mutation?

when there is a two way exchange of genetic portion between two non-homologus chromosomes, its called reciprocal mutation, its a type of translocation mutation


What chromosomal mutation results in alagille syndrome?

translocation


What is the DNA chromosome called that breaks off and reattaches to a homologous chromosome that is paired up in meiosis?

This is a type of mutation called translocation.


A mutation in which a single base is added to or deleted from DNA is called what?

A mutation in which a single base is added to or deleted from DNA is called an insertion or deletion mutation, also known as an indel mutation. This can lead to a shift in the reading frame during translation, causing significant changes in the resulting protein sequence and potentially leading to functional consequences.


Is down syndrome caused by a translocation mutation?

A very small number.


When a piece of chromosome attaches itself to a nonhomologous chromosome the resulting mutation is called?

translocation


What are different types of mutation?

Deletion, insertion, inversion, translocation, and duplication [for the ppl. Who dnt kno!!]


What is the mutation in hemophilia?

Hemophilia is a mutation of either of the genes that make factor VII or IX. Hemophilia A is a mutation of the F8 gene and Hemophilia B is the mutation of the F9 gene. Both of these mutations occur on the sex-linked X chromosome.


Is color blindness a result of translocation or deletion?

Color blindness is typically caused by a genetic mutation affecting the genes responsible for color vision, such as the OPN1LW and OPN1MW genes on the X chromosome. It is not usually associated with translocation or deletion of genetic material.


What mutation is caused by a piece of DNA breaking away from its chromosome and becoming attached to a non-homologous chromosome called?

Translocation


What is the difference between nondisjunction and translocation mutations?

Nondisjunction is a mutation where chromosomes fail to separate properly during cell division, leading to an abnormal number of chromosomes in daughter cells. Translocation is a mutation where a segment of one chromosome breaks off and attaches to another chromosome, potentially disrupting the normal genetic sequence.