Principles of Inheritance and Variation: Class 12 Important Questions with Answers
72 important questions for Class 12 Biology Chapter 4, Principles of Inheritance and Variation, the way they come in the board exam: MCQs, assertion–reason, case-based and short and long answer questions, with answers. Taken from our Class 12 Biology notes for 2026-27.
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Jump to: Practice set: test yourself20 MCQsAssertion–ReasonAnswers to the practice set
Practice set: test yourself
Try every question before looking at the answers below. 64 or more out of 80 means you are ready for the board.
A. Fill in the blanks (1 mark each)
- Mendel studied ___ pairs of contrasting traits in pea.
- The F2 genotypic ratio of a monohybrid cross is ______.
- ABO blood group is controlled by ___ alleles.
- Pink snapdragon F1 shows ______ dominance.
- The chromosomal theory was given by Sutton and ______.
- In grasshoppers males are ______.
- Down's syndrome is trisomy of chromosome ______.
- Haemophilia is ______-linked recessive.
B. True or false? (1 mark each)
- A test cross uses the homozygous recessive parent.
- In snapdragon F2 the phenotypic and genotypic ratios are equal.
- Linked genes assort independently.
- Human skin colour is polygenic.
- Honey bee males develop from fertilised eggs.
- Turner's syndrome is 45, XO.
- Sickle-cell anaemia is X-linked.
- Thalassaemia is a qualitative problem of globin.
C. Very short answer (1 mark each)
- Name the scientist who first mapped genes.
- Gametes produced by AaBbCc.
- Give an example of pleiotropy.
- Who discovered the X body?
- Name the sex determination in birds.
- Genotypes of group A.
- Name a frameshift-causing change.
- Karyotype of Klinefelter's syndrome.
- Which amino acid replaces glutamic acid in HbS?
- Recombination frequency of white–yellow genes in Drosophila.
D. Short answer I (2 marks each)
- State the law of segregation.
- Why is the law of segregation called the law of purity of gametes?
- Distinguish linkage from recombination.
- Explain haplodiploidy in honey bees.
- Give two differences between Mendelian and chromosomal disorders.
- Why are haemophilic females rare?
- What is non-disjunction? Give one disorder it causes.
- Why did Mendel's work remain unrecognised till 1900?
| Section | A /8 | B /8 | C /10 | D /16 | E /18 | F /20 | G (bonus) | Total /80 |
|---|---|---|---|---|---|---|---|---|
| My marks |
Rough work
E. Short answer II (3 marks each)
- Work out a dihybrid test cross and give its ratio.
- Explain the cause and symptoms of phenylketonuria.
- Show by a cross how a colour-blind daughter can be born.
- Describe Morgan's linkage experiment.
- Compare Down's, Klinefelter's and Turner's syndromes.
- Explain why the ABO blood group shows both co-dominance and dominance.
F. Long answer (5 marks each)
- Explain Mendel's three laws with crosses.
- Describe the genetic basis of sickle-cell anaemia and show by a cross how carrier parents may have an affected child.
G. HOTS (higher-order thinking)
- Why do the genes for flower colour and seed shape in pea assort independently?
- Two parents with normal colour vision have a colour-blind son. What are their genotypes?
- Why is the F2 ratio of snapdragon not 3 : 1?
- Can a person of group O be the father of a child of group AB? Explain.
20 MCQs
- Mendel worked on(a) Drosophila (b) snapdragon (c) Pisum sativum (d) maize
- F2 phenotypic ratio of a monohybrid cross(a) 3 : 1 (b) 1 : 2 : 1 (c) 9 : 3 : 3 : 1 (d) 1 : 1
- Test cross ratio for a heterozygote(a) 3 : 1 (b) 9 : 3 : 3 : 1 (c) all dominant (d) 1 : 1
- Gametes from AaBb(a) 2 (b) 4 (c) 8 (d) 16
- Pink F1 in snapdragon shows(a) dominance (b) incomplete dominance (c) co-dominance (d) epistasis
- Blood group AB shows(a) incomplete dominance (b) polygenic inheritance (c) pleiotropy (d) co-dominance
- Number of genotypes in the ABO system(a) 6 (b) 4 (c) 3 (d) 9
- Dihybrid F2 ratio(a) 3 : 1 (b) 1 : 1 : 1 : 1 (c) 9 : 3 : 3 : 1 (d) 1 : 2 : 1
- The chromosomal theory was given by(a) Morgan (b) de Vries (c) Mendel (d) Sutton and Boveri
- Gene mapping was first done by(a) Morgan (b) Sturtevant (c) Henking (d) Bateson
- Human skin colour is an example of(a) pleiotropy (b) co-dominance (c) polygenic inheritance (d) multiple alleles
- Female heterogamety is seen in(a) birds (b) humans (c) grasshopper (d) Drosophila
- Drones of honey bee have(a) 32 chromosomes (b) 16 chromosomes (c) 8 (d) 64
- Sickle-cell anaemia is due to(a) frameshift (b) deletion of a chromosome (c) point mutation (d) trisomy
- Haemophilia is(a) autosomal dominant (b) autosomal recessive (c) Y-linked (d) X-linked recessive
- Phenylketonuria results from lack of an enzyme converting(a) phenylalanine to tyrosine (b) tyrosine to phenylalanine (c) glucose to glycogen (d) none
- Furrowed tongue and palm crease are seen in(a) Down's (b) Turner's (c) Klinefelter's (d) haemophilia
- Klinefelter's karyotype(a) 45, XO (b) 46, XY (c) 47, +21 (d) 47, XXY
- Thalassaemia is mainly(a) a qualitative defect (b) a quantitative defect of globin (c) X-linked (d) chromosomal
- An O child is born to A and B parents; the parents are(a) IAIA, IBIB (b) IAIB, ii (c) IAi, IBi (d) IAi, IBIB
1 (c) · 2 (a) · 3 (d) · 4 (b) · 5 (b) · 6 (d) · 7 (a) · 8 (c) · 9 (d) · 10 (b) · 11 (c) · 12 (a) · 13 (b) · 14 (c) · 15 (d) · 16 (a) · 17 (a) · 18 (d) · 19 (b) · 20 (c)
Assertion–Reason (6)
(a) Both true, R explains A. (b) Both true, R does not explain A. (c) A true, R false. (d) A false, R true.
- A: The F2 of a dihybrid cross shows 9 : 3 : 3 : 1. R: The two pairs of genes assort independently.
- A: Group AB shows co-dominance. R: IA and IB are both expressed in the heterozygote.
- A: Linked genes do not show 9 : 3 : 3 : 1. R: They lie on different chromosomes.
- A: Haemophilic females are rare. R: The mother must be a carrier and the father haemophilic.
- A: In birds the male decides the sex of the offspring. R: The female is ZW.
- A: Down's syndrome is a Mendelian disorder. R: It is caused by an extra chromosome 21.
Key: 1 (a) · 2 (a) · 3 (c) · 4 (a) · 5 (d) · 6 (d)
Answers to the practice set
A. 1. 7 2. 1 : 2 : 1 3. three 4. incomplete 5. Boveri 6. XO 7. 21 8. X
B. 1. T 2. T 3. F 4. T 5. F (unfertilised) 6. T 7. F (autosomal) 8. F (quantitative)
C. 1. Alfred Sturtevant 2. 3. phenylketonuria 4. Henking 5. ZW–ZZ (female heterogamety) 6. IAIA, IAi 7. insertion or deletion of bases 8. 44 + XXY (47) 9. valine 10. 1.3%
D. 1. The two alleles of a gene separate during gamete formation, so each gamete gets only one 2. Each gamete receives only one allele, pure, unblended 3. Linkage: genes on one chromosome stay together; recombination: new (non-parental) combinations by crossing over 4. Fertilised eggs (2n = 32) → females; unfertilised eggs (n = 16) → males by parthenogenesis; males make sperms by mitosis 5. Mendelian: single-gene mutation, Mendelian inheritance (haemophilia); chromosomal: change in chromosome number/structure, not Mendelian (Down's) 6. Mother must be a carrier and father haemophilic, and such females rarely survive 7. Failure of chromatids/chromosomes to separate in cell division; Down's, Turner's or Klinefelter's 8. Communication was poor, his mathematical approach was new, and "factors" had no physical proof
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