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mutation in a single DNA base may have no effect on the phenotype or may have a great effect. the best example on this is sickle cell anaemia.

haemoglobin is formed of 2 alpha chains of protein and 2 beta chains, this is the beginning of the a.a sequence of beta chains: val-his-leu-thr-pro-glu-glu-lys

in some people, the mutation causes the substitution of a single thymine base with adenine. this causes one of the glutamine molecules with valine so the chain is this:

val-his-leu-thr-pro-val-glu-lys .

this very slight change causes the blood to form fibrous structures when it's not combined with oxygen. this causes many rbcs to be useless at transporting oxygen and the fibers may get stuck in capillaries which will prevent unaffected cells from getting through.

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Q: How can mutation in single DNA base affect the production of normal proteins?
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When when a mutation results in no significant change in the production of a of a functional protein?

When a mutation does not change the result of a normal production of a protein is called harmless. This is because it does no harm to the individual.


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