011899189339ecebc9973c24bd650dc63e1bbe50
jnavarr5
  Thu Feb 13 14:24:37 2025 -0800
Fixing a typo in the CIViC track, refs #34371

diff --git src/hg/makeDb/trackDb/human/civic.html src/hg/makeDb/trackDb/human/civic.html
index 0bca5656f8c..300dccec8bd 100644
--- src/hg/makeDb/trackDb/human/civic.html
+++ src/hg/makeDb/trackDb/human/civic.html
@@ -1,27 +1,27 @@
 <h2>Description</h2>
 
 <p>
 This track shows genomic locations for variants in the
 <a href="https://civicdb.org/welcome" target="_blank">CIViC (Clinical
 Interpretation of Variants in Cancer) database</a>. These clinically
 relevant variant interpretations are expert- and crowd-sourced from
 peer-revied literature, clinical trials, and some conference
 abstracts.
 
 <p>
-Each variant's interpretation is in the context of a broder molecular
+Each variant's interpretation is in the context of a broader molecular
 profile: one or more variants grouped together. For example, clinical
 evidence may be relevant to a KRAS G12 mutation on its own, but other
 clinical evidence may relevant for cases with either a mutation in
 KRAS G12 or G13.
 
 <p>
 The primary points of data from the scientific literature are curated
 as Clinical Evidence, which connects to a molecular profile, which in
 turn connects to the variants shown in this track. Groups of evidence
 can become curator Assertions about the relevence of a molecular
 profile.
 
 <p>
 The detail for a feature will list diseases and therapies that have
 been associated with a genomic variant. Visiting the CIViC page for a