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What are different types of mutation?

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


What are the types of chromosomes mutations?

Duplication, translocation, inversion, deletion.


Which do you think is generally most harmful a duplication deletion translocation or inversion?

deletion


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

Deletion, duplication, inversion, translocation.


How many different kinds of mutations are there?

there are four different types of mutations. deletion, duplication, inversion, and translocation.


What are four-types of chromosomal mutations?

Four Types of Chromosomal Mutations include-Duplication-Translocation-Inversion-Deletion


What are 4 types of chromosome structural changes?

The four types of alterations of chromosome structure are deletion, duplication, inversion, and reciprocal translocation. Deletion is the loss of one or more nucleotides from a gene by mutation; the loss of a fragment of a chromosome. Duplication is repition of a part of a chromosome resulting from fusion with a fragment froma homologous chromosome. Duplication can result from an error in meiosis or from mutagenesis. Inversion is a change in a chromosomeresulting from reattachment of a chromosome fragment to the original chromosome, but in a reverse direction. Mutagens and errors during mesosis can cause inversions. Translocation is the attachment of a chromosomal fragment to a nonhomologous chromosome.


What are examples of mutations and describe the consequences?

Examples of mutations include point mutations (substitution, insertion, deletion), chromosomal mutations (duplication, deletion, inversion, translocation), and silent mutations. These mutations can lead to various consequences such as changes in protein structure and function, genetic disorders, and cancer.


Describe four types of mutation resulting from the breakage of chromosome?

Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.


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.


4 chromosome mutations?

Deletion: Part of a chromosome is missing. Duplication: A segment of a chromosome is copied multiple times. Inversion: A segment of a chromosome is reversed in orientation. Translocation: Part of a chromosome breaks off and attaches to another chromosome.


What do the four types of chromosomal mutations do?

The four types of chromosomal mutation are deletion, duplication, inversion and trasnlocation. Deletion is the loss of all or part of a chromosome. Duplication is where a segment of a chromosome is copied. Inversion is where a section of a chromosome is reversed. Translocation is the process in where a part of one chromosome breaks off and attaches to a non-homologous chromosome.