Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.46893085C>TCA117684LRP4c.1585G>A (p.Asp529Asn)
c.1798G>A (p.Asp600Asn)
c.781G>A (p.Asp261Asn)
 ClinVar dbSNP gnomAD v4 COSMIC
11g.46893085C=CA1969140532LRP4c.1585G= (p.Asp529=)
c.1798G= (p.Asp600=)
c.781G= (p.Asp261=)
 dbSNP

Number of alleles fetched