CB1.3 Genetic Variation Comprehensive NCEA Level 1 Study Guide (copy)

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Last updated 12:26 AM on 9/9/26
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23 Terms

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Genetic Variation

The structural, physiological, or functional differences present between individuals of the same species.

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Continuous Variation

Variation displaying a continuous range of quantitative values without distinct categories, controlled by multiple genes and environmental factors.

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Discontinuous Variation

Variation displaying distinct, non-overlapping categories with no intermediate values, such as blood groups.

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Inheritable Variation

Variations encoded in the base sequence of DNA that can be passed to offspring.

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Non-Inheritable Variation

Variations acquired during an individual's lifetime due to environmental factors, not passed to offspring.

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Phenotype

An organism's observable characteristics determined by the genotype and environmental factors.

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Mutation

A permanent, random change in the base sequence of DNA; the ultimate source of new genetic variation.

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Somatic Mutations

Mutations occurring in body cells that cannot be passed to offspring.

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Gametic Mutations

Mutations occurring in sex cells that can be passed to future generations.

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Natural Selection

The process where individuals with advantageous traits survive and reproduce at higher rates, leading to adaptations in populations.

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Peppered Moth Selection

An example of natural selection where dark morphs gained advantages by camouflaging in polluted environments.

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Population Bottleneck

A drastic reduction in population size due to catastrophic events, leading to decreased genetic variation.

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Gene Flow

Migration of individuals into or out of a population, introducing or removing alleles.

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Karyotype

A visual representation of the complete set of chromosomes in a cell, useful for evaluating genetic abnormalities.

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Purebred

An individual homozygous for a specific trait, producing identical offspring when bred with another purebred.

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Test Cross

A genetic test to determine whether a dominant phenotype individual is homozygous or heterozygous.

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Down Syndrome

A genetic disorder caused by an extra copy of chromosome 21 (Trisomy 21).

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Cancer

A condition arising from unrepaired DNA mutations, leading to uncontrolled cell growth.

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Lactose Persistence

A genetic adaptation resulting from a mutation allowing some adults to digest lactose.

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DNA Polymerase

An enzyme that joins nucleotides to synthesize DNA strands during replication.

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Allele

An alternate form or version of a specific gene.

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Gene

A specific section of DNA that codes for a protein and determines a trait.

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Chromosome

A long, coiled length of DNA that contains many genes.