Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.214781165G>CCA331823BARD1c.709C>G (p.Gln237Glu)
c.215+15896C>G (p.=)
c.158+28247C>G (p.=)
c.652C>G (p.Gln218Glu)
c.364+11132C>G (p.=)
n.551C>G
c.*329C>G (p.=)
n.604C>G
c.73+28247C>G (p.=)
n.702C>G
n.645C>G
n.506+11132C>G
c.655C>G (p.Gln219Glu)
c.808C>G (p.Gln270Glu)
n.899C>G
n.674C>G
n.617C>G
n.478+11132C>G
ClinVar dbSNP ExAC gnomAD COSMIC COSMIC
2g.214781165G>ACA10577838BARD1c.709C>T (p.Gln237Ter)
c.215+15896C>T (p.=)
c.158+28247C>T (p.=)
c.652C>T (p.Gln218Ter)
c.364+11132C>T (p.=)
n.551C>T
c.*329C>T (p.=)
n.604C>T
c.73+28247C>T (p.=)
n.702C>T
n.645C>T
n.506+11132C>T
c.655C>T (p.Gln219Ter)
c.808C>T (p.Gln270Ter)
n.899C>T
n.674C>T
n.617C>T
n.478+11132C>T
ClinVar dbSNP

Number of alleles fetched