Point mutation alter the <u>change in single base pair</u> or affect the single amino acid sequence whereas, chromosomal mutation alter <u>the entire chromosomal structure</u> and cause serious disability in a human body.
Further Explanation:
Point mutation is a kind of mutation that <u>occurs in a single nucleotide of nucleic acid</u>. It involves the substitution of single base pair from another that resulted in change in complementary base pair. The <u>process is completed either by insertion and deletion of single base pair from DNA strand</u>. Point mutation occurs in three forms; <u>silent mutation, mis sense mutation and non sense mutation</u>. Silent mutation codes for same amino acid but it don’t have any phenotypic effect, in mis sense mutation base pair code for different amino acid whereas; nonsense codon mutates and form stop codon and cause serious effect.
Chromosomal mutation is completely different from point mutation it <u>affect the complete chromosomal structure</u>. In mainly occur <u>during meiosis and also by some mutagens</u>. The alteration resulted in <u>the change in the chromosome number in a cell and the complete structure of the chromosome is changed</u>. It includes translocation, insertion, deletion, duplication, and inversion. Chromosomal mutation is the reason for <u>Down syndrome and turner syndrome.
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Chromosomal alteration have serious effect on human genetic material than point mutation because point mutation alter the change in single base pair or affect the single amino acid sequence whereas, chromosomal mutation alter the entire chromosomal structure and cause serious disability in a human body.
Learn More:
1. Learn more about meiosis brainly.com/question/1600165
2. Learn more about the process of molecular diffusion in a cell brainly.com/question/1600165
3. Learn more about human sperm and egg cell brainly.com/question/1626319
Answer Details:
Grade: High School
Subjects: Biology
Topic: Mutation
Keywords:
Point mutation, nucleotide, nucleic acid, substitution, complementary, insertion, deletion, chromosomal, alteration, meiosis, mutagens, duplication, inversion, down syndrome, turner syndrome.