Transcription
Transition
Transversion
Frameshift mutation
Transition is a point mutation that changes a purine nucleotide to another purine (A <--> G) or a pyrimidine nucleotide to another pyrimidine (C <-->T). Approximately two out of three single nucleotide polymorphisms are transitions. Transitions can be caused by oxidative deamination and tautomerization So, the correct answer is 'Transition'
List-I | List-II | ||
(A) | 1 mol of H2O to O2 | (I) | 3F |
(B) | 1 mol of MnO-4 to Mn2+ | (II) | 2F |
(C) | 1.5 mol of Ca from molten CaCl2 | (III) | 1F |
(D) | 1 mol of FeO to Fe2O3 | (IV) | 5F |
The term - non-mendelian inheritance refers to any pattern of heredity in which features do not separate according to Mendel's laws. These principles describe how features linked with single genes on chromosomes in the nucleus are passed down through generations.
It is a form of incomplete dominance in which both alleles for the same feature are expressed in the heterozygote at the same time. For example, the MN blood types of humans.
In a heterozygote, the dominant allele does not always completely cover the phenotypic expression of the recessive gene, resulting in an intermediate phenotype which is referred to as "incomplete dominance”.