The CYP17A1 gene is highly polymorphic and many disease causing mutations are present in different populations.
A list of these sequence variants can be found in the supplementary material to the publication
DeVore and Scott, 2012 (Supplementary Table 2. Summary of CYP17A1 mutations, their effects, and structural context).

The alleles with these mutations are hitherto not characterized and therefore no allelic nomenclature has yet been worked out.



 This page was updated 6-Jul-2012 by Sarah C Sim
Questions and comments are always welcome