Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.68357754A>G | CA381611849 | LRP5 | c.593A>G (p.Asn198Ser) c.-1173A>G (n.-1173A>G) c.620A>G (p.Asn207Ser) n.635A>G | ClinVar dbSNP |
11 | g.68357754A= | CA1980639795 | LRP5 | c.593A= (p.Asn198=) c.-1173A= (n.-1173A=) c.620A= (p.Asn207=) n.635A= | dbSNP |