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).
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.
A deleterious mutation has a negative effect on the phenotype, and thus decreases the fitness of the organism. (A harmful mutation)
phylogeny
It is possible for a point mutation to not change the sequence of amino acids in a protein. This will result in the protein being unchanged and will not affect the phenotype.
The phenotype will not be affected with silent mutation and synonymous mutation. It also can be mutated in a coding region that changes the amino acid or changes the protein to be folded.
A backmutation is a mutation in genetics which restores the original sequence and the original phenotype.
Yes, a mutation can occur without affecting the phenotype at all. For example, a point mutation may change a nucleotide in a codon, but sometimes, the codon can still code the same amino acid, so the mRNA strand can still make the same protein.
the mutation may occur in a non-coding region of the gene, resulting in no change to the protein produced. Additionally, the mutation may be silent, meaning it does not alter the amino acid sequence of the protein. In some cases, the organism may have redundant genes that compensate for the mutation, allowing it to function normally.
gene
When DNA replication makes a mistake, it is called a mutation. Mutations can lead to changes in the genetic code that may affect the function of the protein encoded by that DNA sequence.
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.
gene