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. 2017 May 25;18(6):1138. doi: 10.3390/ijms18061138

Table 2.

Studies linking replication timing to mutations.

Mutation type Measurement Higher in References
Germline point mutations Human SNP Late and TTR [118,119,120,121]
Mouse SNP Late [119]
Mouse–rat divergence Late [119,122]
Human–chimp divergence Late [118,119]
Drosophila divergence Late [123]
Somatic point mutations Human cancer Late [124,125,126,127,128,129,130]
Yeast point mutations Yeast URA3 gene Late [131,132]
Insertions Human cancer Early and TTR [126,133,134]
Human iPSC Early [135]
Fly Late [136,137]
Translocations Human cancer Early (and late in [138]) [126,133,138,139,140]
Mammalian divergence TTR/early [134,141]
Deletions Human cancer Late [126]
Human iPSC Late [135]
Fly Early [136]
Fragile sites Cancer Early or late [96,99,142,143,144]
LOH Cancer Early [145]

SNP: single nucleotide polymorphism; TTR: timing transition regions; URA3: yeast gene encoding orotidine-5′-phosphate decarboxylase; iPSC: induced pluripotent stem cells; LOH: loss of heterozygosity.