1f3567f61cb22650d1b347ad5f6fbb7224bb21d2 dschmelt Thu Jan 14 12:16:55 2021 -0800 Adding sessions for multi-Region for refs #26351 diff --git src/hg/makeDb/trackDb/human/covidMuts.html src/hg/makeDb/trackDb/human/covidMuts.html index d47d628..f92b7e5 100644 --- src/hg/makeDb/trackDb/human/covidMuts.html +++ src/hg/makeDb/trackDb/human/covidMuts.html @@ -7,32 +7,35 @@ severe forms of COVID-19 in previously healthy individuals, and those that make certain individuals resistant to infection by the SARS-CoV2 virus despite repeated exposure.

The major feature of the small set of variants in this track is that they are functionally tested to be deleterious and genetically tested to be disease-causing. Specifically, rare variants were predicted to be loss-of-function at human loci known to govern interferon (IFN) immunity to influenza virus in patients with life-threatening COVID-19 pneumonia, relative to subjects with asymptomatic or benign infection. These genetic defects display incomplete penetrance for influenza respiratory distress and only appear clinically upon infection with the more virulent SARS-CoV-2.

Display Conventions

-Only eight genes and few variants are contained in this track. Use the links in the table to -browse the gene of interest: +Only eight genes with 23 variants are contained in this track. +Use the links below to navigate to the gene of interest or view +all eight genes together using the following sessions for +hg38 or +hg19.

Gene Name Human GRCh37/hg19 Assembly Human GRCh38/hg38 Assembly
TLR3 chr4:186990309-187006252 chr4:186069152-186088069