Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.43092031delCA002252BRCA1n.3567del
c.3503del (p.Asn1168MetfsTer?)
c.3377del (p.Asn1126MetfsTer?)
c.3500del (p.Asn1167MetfsTer?)
c.3425del (p.Asn1142MetfsTer?)
c.785-996del (n.785-996del)
c.647-996del (n.647-996del)
c.2615del (p.Asn872MetfsTer?)
c.3380del (p.Asn1127MetfsTer?)
c.3362del (p.Asn1121MetfsTer?)
c.665-996del (n.665-996del)
c.707-996del (n.707-996del)
c.671-996del (n.671-996del)
c.*3286del (n.*3286del)
c.788-996del (n.788-996del)
c.410-996del (n.410-996del)
c.413-996del (n.413-996del)
c.5-28077del (n.5-28077del)
c.-43-17507del (n.-43-17507del)
c.-99+33243del (n.-99+33243del)
n.3639del
n.3680del
 ClinVar dbSNP
17g.43092031dupCA327875BRCA1n.3567dup
c.3503dup (p.Asn1168LysfsTer2)
c.3377dup (p.Asn1126LysfsTer2)
c.3500dup (p.Asn1167LysfsTer2)
c.3425dup (p.Asn1142LysfsTer2)
c.785-996dup (n.785-996dup)
c.647-996dup (n.647-996dup)
c.2615dup (p.Asn872LysfsTer2)
c.3380dup (p.Asn1127LysfsTer2)
c.3362dup (p.Asn1121LysfsTer2)
c.665-996dup (n.665-996dup)
c.707-996dup (n.707-996dup)
c.671-996dup (n.671-996dup)
c.*3286dup (n.*3286dup)
c.788-996dup (n.788-996dup)
c.410-996dup (n.410-996dup)
c.413-996dup (n.413-996dup)
c.5-28077dup (n.5-28077dup)
c.-43-17507dup (n.-43-17507dup)
c.-99+33243dup (n.-99+33243dup)
n.3639dup
n.3680dup
 ClinVar dbSNP

Number of alleles fetched