Frequencies of different mutation types in somatic tissues and oocytes of mothers and pups analyzed separately for the D-loop and outside the D-loop.

p-Values (Fisher’s exact test) were corrected for multiple testing using the method of Benjamini–Hochberg to control the false discovery rate. The “nt sequenced (type)” is the number of sequenced nucleotides that can effectively lead to the observed mutation type.
(XLSX)