BIOL 1108 Lecture Notes - Lecture 1: Noncoding Dna, Allele Frequency, Genotype Frequency

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Contributing factors to phenotype are: genotype: which set of alleles is possessed by an individual, environment where that individual lives. Even though humans have high phenotype variation, humans rank low in overall variation compared to other species, like fruit flies and penguins. Species: individuals that can exchange material through breeding (sharing alleles) Gene pool: all alleles present in all individuals of a species. Populations: interbreeding groups of organisms in the same species living in the same geographical area. Genetic variation source: mutation generates variation, recombination mixes newly generated variation into the population. Somatic mutation: mutation that occurs in body cells; only effects an individual. (cancer) Germline mutation: mutation that occurs in reproductive cells; effects the population. Genome: an organisms complete set of dna, including all of its genes. Because most of the genome consists of non-coding. Dna ( junk dna), most mutations are neutral, having little to no effect on the organism.

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