Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156134910C>GCA018552LMNAc.745C>G (p.Arg249Gly)
n.1120C>G
c.81C>G (p.Cys27Trp)
c.*95C>G (p.=)
c.*544C>G (p.=)
n.438C>G
c.*545C>G (p.=)
c.*216C>G (p.=)
c.502C>G (p.Arg168Gly)
c.409C>G (p.Arg137Gly)
c.448C>G (p.Arg150Gly)
n.90C>G
n.496C>G (p.Arg166Gly)
c.*419C>G (p.=)
n.106C>G
n.994C>G
n.992C>G
ClinVar dbSNP
1g.156134910C>TCA018559LMNAc.745C>T (p.Arg249Trp)
n.1120C>T
c.81C>T (p.Cys27=)
c.*95C>T (p.=)
c.*544C>T (p.=)
n.438C>T
c.*545C>T (p.=)
c.*216C>T (p.=)
c.502C>T (p.Arg168Trp)
c.409C>T (p.Arg137Trp)
c.448C>T (p.Arg150Trp)
n.90C>T
n.496C>T (p.Arg166Trp)
c.*419C>T (p.=)
n.106C>T
n.994C>T
n.992C>T
ClinVar dbSNP

Number of alleles fetched