Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.28725028G>CCA299116CHEK2c.670C>G (p.Arg224Gly)
c.-237C>G (p.=)
c.541C>G (p.Arg181Gly)
n.700C>G (p.Arg234Gly)
c.700C>G (p.Arg234Gly)
c.574-105C>G (p.=)
n.475-105C>G (p.=)
c.445-105C>G (p.=)
c.-123C>G (p.=)
n.762C>G
n.757C>G
c.475-105C>G (p.=)
c.664C>G (p.Arg222Gly)
c.571C>G (p.Arg191Gly)
n.773C>G
n.541C>G (p.Arg181Gly)
n.320-5543C>G (p.=)
c.634C>G (p.Arg212Gly)
n.103C>G (p.Arg35Gly)
n.445-105C>G (p.=)
n.659C>G (p.=)
ClinVar dbSNP
22g.28725028G>ACA117640CHEK2c.670C>T (p.Arg224Cys)
c.-237C>T (p.=)
c.541C>T (p.Arg181Cys)
n.700C>T (p.Arg234Cys)
c.700C>T (p.Arg234Cys)
c.574-105C>T (p.=)
n.475-105C>T (p.=)
c.445-105C>T (p.=)
c.-123C>T (p.=)
n.762C>T
n.757C>T
c.475-105C>T (p.=)
c.664C>T (p.Arg222Cys)
c.571C>T (p.Arg191Cys)
n.773C>T
n.541C>T (p.Arg181Cys)
n.320-5543C>T (p.=)
c.634C>T (p.Arg212Cys)
n.103C>T (p.Arg35Cys)
n.445-105C>T (p.=)
n.659C>T (p.=)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched