Atomos Test Generator Free PYQs ExamsMy practice Log in / Sign up free

Principles of Inheritance and Variation

Previous year questions with solutions · 2000 – 2026

168Questions
34Papers covered
8.91%Weightage 2026▲ 60.4% vs last year
’00
’01
’02
’03
’04
’05
’06
’07
’08
’09
’10
’11
’12
’13
’15
’16
’17
’18
’19
’20
’21
’22
’23
’24
’25
’26
Year-wise statistics questions · papers · average per paper · weightage
YearQuestionsPapersAvg / paperWeightage
2026924.58.91% ▲ 60.4% vs last year
20253135.56% ▼ 47.2% vs last year
2024122610.53% ▲ 32.6% vs last year
20235157.94% ▼ 13.4% vs last year
202212269.16% ▲ 174.8% vs last year
20212123.33% ▼ 58.3% vs last year
20204148.00% ▼ 15.2% vs last year
20195159.43% ▲ 29.7% vs last year
20184147.27% ▼ 17.1% vs last year
20175158.77% ▲ 12.1% vs last year
2016924.57.83% ▲ 42.2% vs last year
20156235.50% ▼ 23.6% vs last year
20138247.21% ▲ 48.5% vs last year
2012522.54.85% ▲ 16.5% vs last year
20114224.17% ▼ 58.3% vs last year
2010924.510.00% ▲ 40% vs last year
20094147.14% ▲ 96.4% vs last year
20082123.64% ▼ 62.9% vs last year
20075159.80% ▼ 35.7% vs last year
200691915.25% ▲ 20.1% vs last year
200581812.70% ▼ 12.7% vs last year
200481814.55% ▲ 12.7% vs last year
200381812.90% ▲ 3.2% vs last year
200281812.50% ▼ 18.1% vs last year
200191915.25% ▲ 64.7% vs last year
20005159.26%

⚠ 1 of these questions are out of the current syllabus (marked on the question).

163 questions · newest paper first · page 5 of 6

Ques. 121AIPMT 2005

A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by -

  1. Superfemaleness
  2. Turner's syndrome
  3. Triploidy
  4. Down's syndrome
Ques. 122AIPMT 2005

Haemophilia is more commonly seen in human males than in human females because -

  1. This disease is due to an X-linked dominant mutation
  2. This disease is due to a Y-linked recessive mutation
  3. This disease is due to an X-linked recessive mutation
  4. A greater proportion of girls die in infancy
Ques. 123AIPMT 2005

Which of the following is not a hereditary disease?

  1. Cretinism
  2. Cystic fibrosis
  3. Haemophilia
  4. Thalassemia
Ques. 124AIPMT 2005

A woman with normal vision, but whose father was colour blind, marries a colour blind man. Suppose that the fourth child of this couple was a boy. This boy -

  1. May be colour blind or may have normal vision
  2. Must have normal colour vision
  3. Must be colour blind
  4. Will be partially colour blind since he is heterozygous for the colour blind mutant allele.
Ques. 125AIPMT 2005

A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by

  1. triploidy
  2. Down’s syndrome
  3. superfemaleness
  4. Turner’s syndrome
Ques. 126AIPMT 2004

In a plant, red fruit (R) is dominant over yellow fruit (r) and tallness (T) is dominant over shortness (t). If a plant with RRTt genotype is crossed with a plant that is rrtt

  1. 75% will be tall with red fruit
  2. 25% will be tall with red fruit
  3. 50% will be tall with red fruit
  4. All the offspring will be tall with red fruit
Ques. 127AIPMT 2004

A male human is heterozygous for autosomal genes A and B and is also hemizygous for hemophilic gene h. What proportion of his sperms will be abh?

  1. 1/16
  2. 1/32
  3. 1/8
  4. 1/4
Ques. 128AIPMT 2004

Lack of independent assortment of two genes A and B in fruit fly Drosophila is due to

  1. Linkage
  2. Recombination
  3. Repulsion
  4. Crossing over
Ques. 129AIPMT 2004

One of the parents of a cross has a mutation in its mitochondria. In that cross, that parent is taken as a male. During segregation of F2 progenies that mutation is found in -

  1. 50% of the progenies
  2. 1/3 of the progenies
  3. None of the progenies
  4. All the progenies
Ques. 130AIPMT 2004

A normal woman, whose father was colour-blind is married to a normal man. The sons would be :-

  1. All colour-blind
  2. 75% colour-blind
  3. All normal
  4. 50% colour-blind
Ques. 131AIPMT 2004

The recessive genes located on X-chromosomes in humans are always -

  1. Expressed in females
  2. Sub-lethal
  3. Expressed in males
  4. Lethal
Ques. 132AIPMT 2004

After a mutation at a genetic locus the character of an organism changes due to the change in :-

  1. Protein synthesis pattern
  2. RNA transcription pattern
  3. DNA replication
  4. Protein structure
Ques. 133AIPMT 2004

In a mutational event, when adenine is replaced by guanine, it is a case of -

  1. Frameshift mutation
  2. Transition
  3. Transversion
  4. Transcription
Ques. 134AIPMT 2003

Which one of the following traits of garden pea studied by Mendel was a recessive feature?

  1. Green seed colour
  2. Green pod colour
  3. Axial flower position
  4. Round seed shape
Ques. 135AIPMT 2003

The genes controlling the seven pea characters studied by Mendel are now known to be located on how many different chromosomes?

  1. Six
  2. Seven
  3. Five
  4. Four
Ques. 136AIPMT 2003

Two crosses between the same pair of genotypes or phenotypes in which the sources of the gametes are reversed in one cross, is known as:

  1. Reciprocal cross
  2. Reverse cross
  3. Test cross
  4. Dihybrid cross
Ques. 137AIPMT 2003

Pattern baldness, moustaches and beard in human males are examples of:

  1. Sex limited traits
  2. Sex influenced traits
  3. Sex determining traits
  4. Sex linked traits
Ques. 138AIPMT 2003

Which one of the following conditions though harmful in itself, is also a potential saviour from a mosquito borne infectious disease?

  1. Pernicious anaemia
  2. Thalassaemia
  3. Leukemia
  4. Sickle cell anaemia
Ques. 139AIPMT 2003

Down's syndrome is caused by an extra copy of chromosome number 21. What percentage of offspring produced by an affected mother and a normal father would be affected by this disorder?

  1. 50%
  2. 100%
  3. 75%
  4. 25%
Ques. 140AIPMT 2003

In Drosophila, the sex is determined by:

  1. X and Y chromosomes
  2. Whether the egg is fertilized or develops parthenogenetically
  3. The ratio of number of X-chromosomes to the sets of autosomes
  4. The ratio of pairs of X-chromosomes to the pairs of autosomes
Ques. 141AIPMT 2003

Christmas disease is another name for :-

  1. Hepatitis B
  2. Sleeping sickness
  3. Haemophilia B
  4. Down's syndrome
Ques. 142AIPMT 2002

Which of the following is the example of pleiotropy ?

  1. Thalassemia
  2. Haemophilia
  3. Sickle cell anaemia
  4. Colour blindness
Ques. 143AIPMT 2002

There are three genes a, b and c. The percentage of crossing over between a and b is 20%, b and c is 28% and a and c is 8%. What is the sequence of genes on chromosome?

  1. a, b, c
  2. b, a, c
  3. a, c, b
  4. None
Ques. 144AIPMT 2002

On selfing a plant of F1 generation with genotype “AABbCC”, the phenotypic ratio in F2 generation will be

  1. 1 : 1
  2. 3 : 1
  3. 9 : 3 : 3 : 1
  4. 27 : 9 : 9 : 9 : 3 : 3 : 3 : 1
Ques. 145AIPMT 2002

A gene is said to be dominant if : -

  1. It is expressed only in heterozygous condition
  2. It expresses its effect only in homozygous stage
  3. It is never expressed in any condition
  4. It is expressed both in homozygous and heterozygous condition
Ques. 146AIPMT 2002

A diseased man marries a normal woman. They get three daughters and five sons. All the daughters were diseased and sons were normal. The gene of this disease is : -

  1. Sex linked dominant
  2. Autosomal dominant
  3. Sex linked recessive
  4. Sex limited character
Ques. 147AIPMT 2002

Which of the following is a correct match -

  1. Sickle cell anaemia = X – Chromosome
  2. Down Syndrome = 21st Chromosome
  3. Haemophilia = Y – Chromosome
  4. Parkinson Disease = X & Y Chromosome
Ques. 148AIPMT 2002

Change in sequence of nucleotide in DNA is called as -

  1. Recombination
  2. Mutation
  3. Mutagen
  4. Translation
Ques. 149AIPMT 2002

If a diploid cell is treated with colchicine then it becomes : -

  1. Tetraploid
  2. Monoploid
  3. Diploid
  4. Triploid
Ques. 150AIPMT 2001

Two non-allelic genes produce the new phenotype when present together but fail to do so independently then it is called

  1. Polygene
  2. Complementary gene
  3. Non-complementary gene
  4. Epistasis