APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context

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Figure 5.
Figure 5.

Density of linked SNPs 5′ and 3′ of a TpCpW→K mutation. In the schematic depiction of a replication fork at the top of the figure, red asterisks correspond to de novo mutations, and AP/U is the position of the TpCpW→G mutation interpreted as the position of the abasic site or the position of the TpCpW→T mutation interpreted as the position of the uracil. The rate of mutations on the lagging (AD) or the leading (EH) strand is measured in five nonoverlapping 1-kb windows at increasing distance from the TpCpW→K SNPs. (***) P < 0.001; (**) P < 0.01; (*) P < 0.05 (χ2 test).

This Article

  1. Genome Res. 27: 175-184

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