Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.11105319C>ACA404076380LDLRc.671C>A (p.Ser224Ter)
c.413C>A (p.Ser138Ter)
c.667C>A
c.314-2073C>A (n.314-2073C>A)
c.290C>A (p.Ser97Ter)
c.314-1246C>A (n.314-1246C>A)
c.13C>A
n.563C>A
n.530C>A
ClinVar dbSNP
19g.11105319C>GCA043464LDLRc.671C>G (p.Ser224Ter)
c.413C>G (p.Ser138Ter)
c.667C>G
c.314-2073C>G (n.314-2073C>G)
c.290C>G (p.Ser97Ter)
c.314-1246C>G (n.314-1246C>G)
c.13C>G
n.563C>G
n.530C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.11105319C=CA2322767363LDLRc.671C= (p.Ser224=)
c.413C= (p.Ser138=)
c.667C=
c.314-2073C= (n.314-2073C=)
c.290C= (p.Ser97=)
c.314-1246C= (n.314-1246C=)
c.13C=
n.563C=
n.530C=
dbSNP
19g.11105319C>TCA404076381LDLRc.671C>T (p.Ser224Leu)
c.413C>T (p.Ser138Leu)
c.667C>T
c.314-2073C>T (n.314-2073C>T)
c.290C>T (p.Ser97Leu)
c.314-1246C>T (n.314-1246C>T)
c.13C>T
n.563C>T
n.530C>T
ClinVar dbSNP gnomAD v4

Number of alleles fetched