Heritable change in DNA sequence. Point (substitution, insertion, deletion), structural (inversion, translocation, CNV), or aneuploidy. Rate ~10⁻⁹ per base per replication in humans.
Heritable change in DNA sequence. Point (substitution, insertion, deletion), structural (inversion, translocation, CNV), or aneuploidy. Rate ~10⁻⁹ per base per replication in humans.