Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.46894748T>GCA117688LRP4c.1381A>C (p.Thr461Pro)
c.1594A>C (p.Thr532Pro)
c.577A>C (p.Thr193Pro)
ClinVar dbSNP
11g.46894748T>CCA380285845LRP4c.1381A>G (p.Thr461Ala)
c.1594A>G (p.Thr532Ala)
c.577A>G (p.Thr193Ala)
dbSNP gnomAD v2 gnomAD v4
11g.46894748T>ACA380285843LRP4c.1381A>T (p.Thr461Ser)
c.1594A>T (p.Thr532Ser)
c.577A>T (p.Thr193Ser)
dbSNP gnomAD v4
11g.46894748T=CA1969144893LRP4c.1381A= (p.Thr461=)
c.1594A= (p.Thr532=)
c.577A= (p.Thr193=)
dbSNP

Number of alleles fetched