DNV/MNV detection

[Bioinfowangm]

Hi there,

I have been using Strelka2 for somatic mutation call. For di-nucleotide variants, such as CC>TT mutations which can be frequent in UV exposed cancers, it seems that these mutations were treated as multiple separate C>T variants. I wonder if there is a way to output these DNVs (and MNVs) as a single mutation, rather than multiple different variants. Thanks!