Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.11105384T>GCA10584940LDLRc.736T>G (p.Cys246Gly)
c.478T>G (p.Cys160Gly)
c.732T>G
c.314-2008T>G (n.314-2008T>G)
c.355T>G (p.Cys119Gly)
c.314-1181T>G (n.314-1181T>G)
c.78T>G
n.628T>G
n.595T>G
ClinVar dbSNP
19g.11105384T>ACA404076699LDLRc.736T>A (p.Cys246Ser)
c.478T>A (p.Cys160Ser)
c.732T>A
c.314-2008T>A (n.314-2008T>A)
c.355T>A (p.Cys119Ser)
c.314-1181T>A (n.314-1181T>A)
c.78T>A
n.628T>A
n.595T>A
ClinVar dbSNP
19g.11105384T>CCA10584939LDLRc.736T>C (p.Cys246Arg)
c.478T>C (p.Cys160Arg)
c.732T>C
c.314-2008T>C (n.314-2008T>C)
c.355T>C (p.Cys119Arg)
c.314-1181T>C (n.314-1181T>C)
c.78T>C
n.628T>C
n.595T>C
ClinVar dbSNP
19g.11105384T=CA2322767414LDLRc.736T= (p.Cys246=)
c.478T= (p.Cys160=)
c.732T=
c.314-2008T= (n.314-2008T=)
c.355T= (p.Cys119=)
c.314-1181T= (n.314-1181T=)
c.78T=
n.628T=
n.595T=
dbSNP

Number of alleles fetched