this is the genetic observable characteristic of an organism which is variated by gene or chromosome mutation
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The phenotype of a mutation refers to the observable physical or biochemical characteristics of an organism that result from the mutation. It can include traits such as altered appearance, behavior, or function compared to the wild-type or non-mutated organism.
Mutation occurs, if a mutation is recessive it is not expressed in the phenotype, if however it is dominant when passed on in the offspring it is expressed in the phenotype.
phylogeny
A backmutation is a mutation in genetics which restores the original sequence and the original phenotype.
The Bombay phenotype is caused by a homozygous recessive mutation in the FUT1 gene, which results in the absence of H antigen on red blood cells. Therefore, the genotype for the Bombay phenotype is hh.
Mutations in introns are less likely to affect phenotype because introns are not translated into protein, unlike exons which contain coding regions for proteins. Introns are involved in regulation of gene expression through processes such as alternative splicing, but mutations within introns typically have a more subtle impact on gene expression compared to mutations in coding regions (exons).