DOVE: DMD Open-access Variant Explorer


Input specific DMD gene variants to receive analysis of variant type, length, reading frame alterations, potential effects on splicing, and exon skipping eligibility.


 Text input

Input should include a reference to:

  1. The location of the variant (nucleotide positions should be relative to cDNA (NM_004006.2).
  2. The type of variant.
  Click for examples of acceptable input

 Exon deletion selector