7324d595d6a645c91238b9ab40c752eb8272660c
lrnassar
  Mon Sep 30 11:32:15 2019 -0700
Making some changes from CR refs #24232

diff --git src/hg/makeDb/trackDb/human/mastermind.html src/hg/makeDb/trackDb/human/mastermind.html
index d4b33b1..5769e0e 100644
--- src/hg/makeDb/trackDb/human/mastermind.html
+++ src/hg/makeDb/trackDb/human/mastermind.html
@@ -22,34 +22,34 @@
 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>As suggested by Genomenom, we added a filter on all variants, so the data is not exactly identical 
+<p>As suggested by Genomenom, we added a filter on all variants, so the data are not exactly identical 
 to their website. We skip 
-variants with more than one nucleotide and a MMCNT of 0 and where the variant is not an indel, 
-meaning that for longer variants, only variants are shown that are explicitly
+variants with more than one nucleotide and a MMCNT of 0 and where the variant is not an indel. 
+This means that for longer variants, only variants are shown that are explicitly
 mentioned in the papers. This makes the data more specific.
 </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>