95d62eaffe46026207539ae1d1e815c1c83779ff
lrnassar
  Fri Mar 14 17:24:32 2025 -0700
Fixing the revel values, I accidentally makde the wrong boundaries in my first pass, refs #35352

diff --git src/hg/makeDb/trackDb/human/revel.html src/hg/makeDb/trackDb/human/revel.html
index ee6f315af22..095ab2f787b 100644
--- src/hg/makeDb/trackDb/human/revel.html
+++ src/hg/makeDb/trackDb/human/revel.html
@@ -84,39 +84,39 @@
 </p>
 
 <p><b>Track colors</b></p>
 <p>
 This track is colored according to <a target="_blank" href="https://www.sciencedirect.com/science/article/pii/S000292972200461X">Table 2 in Vikas et al</a>. The colors represent the recommended ACMG/AMP score cutoffs.
 
 <table style="text-align: left;">
   <thead>
     <tr>
       <th>Range</th>
       <th>Classification</th>
     </tr>
   </thead>
   <tbody>
     <tr>
-      <td>&ge; .773</td>
+      <td>&ge; .644</td>
       <td style="color: rgb(255,0,0);">Pathogenic</td>
     </tr>
     <tr>
-      <td>.772 - .184</td>
+      <td>.643 - .291</td>
       <td style="color: rgb(192,192,192);">Neutral</td>
     </tr>
     <tr>
-      <td>&le; .183</td>
+      <td>&le; .290</td>
       <td style="color: rgb(80,166,230);">Benign</td>
     </tr>
   </tbody>
 </table>
 
 <p>For hg38, note that the data was converted from the hg19 data using the UCSC
 liftOver program, by the REVEL authors. This can lead to missing values or
 duplicated values. When a hg38 position is annotated with two scores due to the
 lifting, the authors removed all the scores for this position. They did the same when
 the reference allele has changed from hg19 to hg38.  Also, on hg38, the track has
 the "lifted" icon to indicate
 this. You can double-check if a nucleotide
 position is possibly affected by the lifting procedure by activating the track
 "Hg19 Mapping" under "Mapping and Sequencing".
 </p>