person’s <u>genotype</u> is their unique sequence of DNA. More specifically, this term is used to refer to the two alleles a person has inherited for a particular gene. <u>Phenotype</u> is the detectable expression of this genotype – a patient’s clinical presentation.
Explanation:
person’s phenotype results from the interaction between their genotype and their environment.
The connection between genotype and phenotype is not always clear-cut. This means that you may encounter disparities between your patient’s genomic test result and their clinical presentation. Similarly, the phenotype of patients with a given genetic condition may vary greatly even within families.
3.Even though there are some dna traces in the mitochondria,it’s won’t really be tested for gcse and mostly the DNAs are found in the nucleus of the cell.
