Solution
Core Logic
Sickle-cell anaemia is an autosome-linked recessive trait. At the molecular level, it is caused by a point mutation leading to a single amino acid substitution: Glutamic acid (Glu) is replaced by Valine (Val) at the sixth position of the beta-globin chain of the haemoglobin molecule. This occurs due to a single base substitution at the sixth codon of the beta-globin gene from GAG to GUG.
Step 1: Final Conclusion
This specific substitution is the classic hallmark of Sickle-cell anaemia.
Pattern Recognition
GAG to GUG -> Glu to Val -> position 6 of beta-globin = Sickle-cell anaemia. Universally tested standard fact.
Chapter Mix
Class 12 Biology: Principles of Inheritance and Variation Class 12 Biology: Molecular Basis of Inheritance