List of variants reported as pathogenic for Breast-ovarian cancer, familial, susceptibility to, 3; Fanconi anemia complementation group O by Fulgent Genetics, Fulgent Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	rs200293302	0.00004
NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter)	rs730881939	0.00002
NM_058216.3(RAD51C):c.706-2A>G	rs587780259	0.00002
NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	rs770637624	0.00001
NM_058216.3(RAD51C):c.905-2_905-1del	rs587781995	0.00001
NM_058216.3(RAD51C):c.955C>T (p.Arg319Ter)	rs587781287	0.00001
NM_058216.3(RAD51C):c.97C>T (p.Gln33Ter)	rs587782528	0.00001
NM_058216.3(RAD51C):c.1026+5_1026+7del	rs587781410
NM_058216.3(RAD51C):c.186_187del (p.Gln62fs)	rs587782170
NM_058216.3(RAD51C):c.394dup (p.Thr132fs)	rs730881940
NM_058216.3(RAD51C):c.525dup (p.Cys176fs)	rs768793789
NM_058216.3(RAD51C):c.653_654del (p.Glu218fs)	rs587782286
NM_058216.3(RAD51C):c.701C>G (p.Ser234Ter)	rs587782818

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