Explanation: Mutation is a sudden, stable and heritable change in genetic material.
Explanation: Mutations create new alleles.
Explanation: Normal haemoglobin contains glutamic acid.
Explanation: Reading frame changes.
Explanation: Silent mutations code for the same amino acid.
Explanation: Nonsense mutations introduce a stop codon, ending protein synthesis early.
Explanation: Chromosomal mutations involve structural changes in chromosomes.
Explanation: Deletion removes a part of the chromosome.
Explanation: Inversion reverses the orientation of a chromosomal segment.
Explanation: Translocation involves exchange of segments between different chromosomes.
Explanation: Duplication produces an extra copy of a gene, increasing gene dosage.
Explanation: Genome mutations alter the number of chromosomes.
Explanation: Trisomy is a type of aneuploidy involving an extra chromosome.
Explanation: Down syndrome results from an extra copy of chromosome 21.
Explanation: Turner syndrome is caused by monosomy of the X chromosome.
Explanation: Klinefelter syndrome occurs due to an extra X chromosome in males.
Explanation: Plants tolerate polyploidy well and it is common among them.
Explanation: Spontaneous mutations occur without external agents.
Explanation: External mutagens induce mutations.
Explanation: UV radiation induces thymine–thymine dimers in DNA.
Explanation: Nitrous acid alters base pairing by deamination.
Explanation: Some viruses act as biological mutagens via transposition.
Explanation: Somatic mutations affect body cells only.
Explanation: Germ cell mutations are inherited and drive evolution.
Explanation: Cancer results from accumulation of somatic mutations.
Explanation: Frameshift mutations alter the entire reading frame.
Explanation: Neutral mutations produce no observable effect.
Explanation: Mutations generate genetic variation essential for adaptation.
Explanation: Missense mutation replaces one amino acid with another.
Explanation: Cytosine deaminates to uracil.
Explanation: Point mutation occurs at gene level, not chromosome structure.
Explanation: Polyploidy involves change in chromosome sets.
Explanation: Addition or loss of nucleotides shifts the reading frame.
Explanation: Nonsense mutation introduces a premature stop codon.
Explanation: Failure of chromosome separation leads to aneuploidy.
Explanation: Some mutations enhance survival, such as antibiotic resistance.
Explanation: Aneuploidy involves gain or loss of chromosomes.
Explanation: Mutagens increase the frequency of mutations.
Explanation: Cri du chat syndrome is caused by deletion of the short arm of chromosome 5.
Explanation: Silent mutations do not change the amino acid sequence.
Explanation: Transposons move within the genome, disrupting genes.
Explanation: Mutations create variation driving evolution.
Explanation: Mutagens alter DNA structure or sequence.
Explanation: Frameshift mutations disrupt the entire protein sequence.
Explanation: Sickle cell anaemia results from a single base substitution.
Explanation: Aneuploidy involves chromosome number, not structure.
Explanation: Silent mutations do not alter the amino acid sequence.
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