it is caused by substitution in your DNA and causes a harmful change the only benifet from this is protection against malaria
The mutation that results in the replacement of glutamate with valine in sickle cell anemia is a missense mutation. This type of mutation occurs when a single nucleotide change in the DNA sequence leads to the substitution of one amino acid for another in the resulting protein. In this case, the specific change involves the codon for glutamic acid being altered to code for valine, which affects the hemoglobin structure and function.
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
Mutations in the hemoglobin molecules cause sickle cell anemia.
The type of mutation that causes a defect in the gene (causing sickle cell anaemia) is a substitution mutation.A single nucleotide substitution (A to T) in the β-globin gene causes the amino acid valine to replace glutamic acid. This changes the resulting protein, causing a haemoglobin with an abnormal shape to be created.
Deletion Mutation causes DiGeorges Syndrome.
A frameshift mutation in the CARD15 gene
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deletion
The mutation that causes Autism is a rare genetic mutation. There are three different genes that are linked to the cause of different disorders on the Autism Spectrum.
Unknown at this time.
A certain substitution in human DNA changes the code for hemoglobin; this ultimately results in sickle-cell anima.
It's a gene mutation. And it is different for each organ.