c0401cde5d3035571adf6898d572a60f756d0af2
angie
  Mon Nov 18 15:36:10 2019 -0800
dbSnp153: Use new FilterLabel setting to replace the long definition of numeric maxFuncImpact column with a label that is more congruent with dropdown choices.  refs #23283

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index 2a2af37..6daab29 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -1656,30 +1656,31 @@
         freqNotRefAlt|Reference genome allele is not major allele in at least one project,\
         multiMap|Variant is placed in more than one genomic position,\
         otherMapErr|Another mapping of this variant has illegal coords (indel mapping error?),\
         overlapDiffClass|Variant overlaps other variant(s) of different type/class,\
         overlapSameClass|Variant overlaps other variant(s) of same type/class but different position,\
         rareAll|MAF < 1% in all projects that report frequencies (or no frequency data),\
         rareSome|MAF < 1% in at least one project that reports frequencies,\
         refIsAmbiguous|Reference genome allele contains IUPAC ambiguous base(s),\
         refIsMinor|Reference genome allele is minor allele in at least one project that reports frequencies,\
         refIsRare|Reference genome allele frequency is <1% in at least one project,\
         refIsSingleton|Reference genome frequency is 0 in all projects that report frequencies,\
         refMismatch|Reference allele mismatches reference genome sequence,\
         revStrand|Variant maps to opposite strand relative to dbSNP's preferred top-level placement
 #'
     ucscNotesFilterType multipleListOr
+    maxFuncImpactFilterLabel Greatest functional impact on gene
     maxFuncImpactFilterValues 0|(not annotated),\
         0865|frameshift,\
         1587|stop_gained,\
         1574|splice_acceptor_variant,\
         1575|splice_donor_variant,\
         1821|inframe_insertion,\
         1583|missense_variant,\
         1590|terminator_codon_variant,\
         1819|synonymous_variant,\
         1580|coding_sequence_variant,\
         1623|5_prime_UTR_variant,\
         1624|3_prime_UTR_variant,\
         1619|nc_transcript_variant,\
         2153|genic_upstream_transcript_variant,\
         1986|upstream_transcript_variant,\