5a185db3a16a454b4e9b6c39e803b3c88aa58b33
max
  Wed Sep 25 02:27:16 2019 -0700
fix suggested by qa, refs #24157

diff --git src/hg/makeDb/trackDb/human/mastermind.html src/hg/makeDb/trackDb/human/mastermind.html
index 8c9024b..a8b2b13 100644
--- src/hg/makeDb/trackDb/human/mastermind.html
+++ src/hg/makeDb/trackDb/human/mastermind.html
@@ -22,34 +22,35 @@
 page</a> page. Advanced features require a license for the
 <a href="https://www.genomenon.com/mastermind-pro-upgrade/" target="_blank">Mastermind Professional Edition</a>, 
 which contains the same content but allows more comprehensive searches.
 </p>
 
 <h2>Display Conventions and Configuration</h2>
 
 <p>
 Genomic locations of variants are labeled with the nucleotide change.
 Hover over the features to see the gene, the amino acid change and the scores MMCNT1, MMCNT2 and 
 MMCNT3, described below. All other information is shown on the respective Mastermind variant detail
 page, accessible via the &quot;Protein change and link to details&quot; at the top of the details page. The
 features are colored based on their evidence:
 </p>
 
-<p>In Sep 2019, suggested by Genomenom, we added a filter on all variants. From then on, we skip variants with more than 
-one nucleotide and MMCNT is 0 and where the variant is not an idel, meaning
+<p>As suggested by Genomenom, we added a filter on all variants to make the
+ We skip variants with more than one
+nucleotide and where MMCNT0 is 0 and where the variant is not an idel, meaning
 that for longer variants, only variants are shown that are explicitely
-mentioned in the papers. This makes the data more specific.
+mentioned in the papers.
 </p>
 
 <p>
 <table>
   <thead>
   <tr>
     <th style="border-bottom: 2px solid #6678B1;">Color</th>
     <th style="border-bottom: 2px solid #6678B1;">Level of support</th>
   </tr>
   </thead>
   <tr>
     <th bgcolor="#0C0C78"></th>
     <th align="left">High: at least one paper mentions this exact cDNA change</th>
   </tr>
   <tr>