Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.11113643C>GCA023505LDLRc.1725C>G (p.Tyr575Ter)
c.1467C>G (p.Tyr489Ter)
c.1347C>G (p.Tyr449Ter)
c.1721C>G
c.963C>G (p.Tyr321Ter)
c.1344C>G (p.Tyr448Ter)
c.1086C>G (p.Tyr362Ter)
c.188C>G
n.1617C>G
n.1584C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.11113643C>ACA404086227LDLRc.1725C>A (p.Tyr575Ter)
c.1467C>A (p.Tyr489Ter)
c.1347C>A (p.Tyr449Ter)
c.1721C>A
c.963C>A (p.Tyr321Ter)
c.1344C>A (p.Tyr448Ter)
c.1086C>A (p.Tyr362Ter)
c.188C>A
n.1617C>A
n.1584C>A
ClinVar dbSNP
19g.11113643C>TCA505743158LDLRc.1725C>T (p.Tyr575=)
c.1467C>T (p.Tyr489=)
c.1347C>T (p.Tyr449=)
c.1721C>T
c.963C>T (p.Tyr321=)
c.1344C>T (p.Tyr448=)
c.1086C>T (p.Tyr362=)
c.188C>T
n.1617C>T
n.1584C>T
ClinVar dbSNP

Number of alleles fetched