mutation is a permanent change in the DNA sequence of a gene and can alter the amino acid sequence of the protein encoded by the gene..
tt
during meiosis
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
You can have a baby with physical/mental deformities or death of the child.
Deletion: loss of a chromosomal segment. Duplication: repetition of a chromosomal segment. Inversion: reversal of a chromosomal segment. Translocation: movement of a chromosomal segment to a new location on a different chromosome.
Chromosomal mutation can have lasting impacts on the person who this happens to. A version of a chromosomal mutation is the mutation that leads to Down's Syndrome.
chromosomal mutation
a gene is passed on from generations and a chromosome is just found in certain cells
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gene mutation, chromosomal abberations
During meiosis
during meiosis
Nope, what you're thinking of is actually called an inversion mutation (a type of structural aberration); a chromosomal mutation is simply any sort of mutation that affects an organism's genotype.
Yes
Chromosomal mutation
translocation
during meiosis