Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.43092851delCA001762BRCA1n.2746del
c.2682del (p.Lys894AsnfsTer?)
c.2556del (p.Lys852AsnfsTer?)
c.2679del (p.Lys893AsnfsTer?)
c.2604del (p.Lys868AsnfsTer?)
c.785-1817del (n.785-1817del)
c.647-1817del (n.647-1817del)
c.1794del (p.Lys598AsnfsTer?)
c.2559del (p.Lys853AsnfsTer?)
c.2541del (p.Lys847AsnfsTer?)
c.665-1817del (n.665-1817del)
c.707-1817del (n.707-1817del)
c.671-1817del (n.671-1817del)
c.*2465del (n.*2465del)
c.788-1817del (n.788-1817del)
c.410-1817del (n.410-1817del)
c.413-1817del (n.413-1817del)
c.5-28898del (n.5-28898del)
c.-43-18328del (n.-43-18328del)
c.-99+32422del (n.-99+32422del)
n.2818del
n.2859del
 ClinVar dbSNP
17g.43092850_43092851delCA001761BRCA1n.2745_2746del
c.2681_2682del (p.Lys894ThrfsTer8)
c.2555_2556del (p.Lys852ThrfsTer8)
c.2678_2679del (p.Lys893ThrfsTer8)
c.2603_2604del (p.Lys868ThrfsTer8)
c.785-1818_785-1817del (n.785-1818_785-1817del)
c.647-1818_647-1817del (n.647-1818_647-1817del)
c.1793_1794del (p.Lys598ThrfsTer8)
c.2558_2559del (p.Lys853ThrfsTer8)
c.2540_2541del (p.Lys847ThrfsTer8)
c.665-1818_665-1817del (n.665-1818_665-1817del)
c.707-1818_707-1817del (n.707-1818_707-1817del)
c.671-1818_671-1817del (n.671-1818_671-1817del)
c.*2464_*2465del (n.*2464_*2465del)
c.788-1818_788-1817del (n.788-1818_788-1817del)
c.410-1818_410-1817del (n.410-1818_410-1817del)
c.413-1818_413-1817del (n.413-1818_413-1817del)
c.5-28899_5-28898del (n.5-28899_5-28898del)
c.-43-18329_-43-18328del (n.-43-18329_-43-18328del)
c.-99+32421_-99+32422del (n.-99+32421_-99+32422del)
n.2817_2818del
n.2858_2859del
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched