7555d3078ece791540738922db687996c4c82b1b jnavarr5 Wed Sep 2 11:43:14 2026 -0700 Adding Eliza's session URL now that it is ready, refs #37763 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 78228ada2b5..dbd76d1f2b4 100644 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -172,32 +172,31 @@ Scores range from 0 to 1, with higher values indicating a greater predicted likelihood that a variant is disease-relevant. As with any pathogenicity prediction score, EVE is intended as supporting evidence rather than a stand-alone classifier.

Each track entry spans one protein at its genomic locus. The heatmap columns correspond to individual amino acid positions, placed at the codon's genomic coordinate, and the rows correspond to the 20 standard amino acids, ordered by amino acid class. Each cell shows the EVE score for substituting the wildtype amino acid at that position with the row amino acid. Empty cells indicate the wildtype amino acid at a given position, or positions for which no score is available.

- + Genome Browser screenshot of the EVE track at the HGF locus on hg38

EVE missense variant effect scores for the HGF locus (chr7, GRCh38/hg38). Each row is an amino acid substitution; each column is a protein position. Hovering over a cell shows the substitution and EVE score.

Items in this track are colored according to score: