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Single Substitution Mutation
Insertion Mutation (INDEL)
A type of point mutation where extra bases are added into the DNA sequence.
Deletion Mutation (INDEL)
A type of point mutation where bases are removed from the DNA.
A type of missense mutation that changes the amino acid but does not significantly affect the protein (polar to polar).

A type of misses mutation that changes the amino acid from polar to non polar vise versa

Somatic Mutation
A mutation that occurs in non-germline cells and is not inherited, often affecting only the individual organism. (Body cells)
Germ-line Mutation
A mutation that occurs in the germ cells (sperm and eggs) and can be passed on to offspring, potentially affecting future generations.
Transversion Mutation
A type of point mutation (Single base Substitution) where a purine is replaced by a pyrimidine or vice versa, leading to changes in DNA sequence.
Transition Mutation
A type of point mutation (Single Base Substitution) where a purine is substituted for another purine or a pyrimidine for another pyrimidine, resulting in a change in the DNA sequence.
Silent Mutation
A mutation that doesn’t effect normal, cannot tell there is a mutation (NONE in everything) same genetic code!

Deleterious Mutation
A mutation that is harmful to an organism, often resulting in reduced fitness or negative effects on survival and reproduction.
Beneficial Mutation
A mutation that enhances an organism's fitness, leading to improved survival or reproduction in a specific environment.
Neutral Mutation
A mutation that has no significant effect on the organism's fitness, neither beneficial nor harmful.
Nonsense Mutation
a DNA change that causes a protein to stop being made early

Missense Mutation
type of point mutation (Single base substitution) in which a single nucleotide change in a DNA sequence results in the substitution of one amino acid for another in the protein produced.

A, G
PURINE

C, T, U
PYRIMIDINE
