List of variants reported as pathogenic for Familial cancer of breast; Fanconi anemia complementation group J by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1372G>T (p.Glu458Ter)	rs587780228	0.00003
NM_032043.3(BRIP1):c.1240C>T (p.Gln414Ter)	rs368796923	0.00001
NM_032043.3(BRIP1):c.1236del (p.Val413fs)	rs863224525
NM_032043.3(BRIP1):c.133G>T (p.Glu45Ter)	rs587781292
NM_032043.3(BRIP1):c.141del (p.Thr48fs)	rs587782065
NM_032043.3(BRIP1):c.2576-1G>A	rs587782539
NM_032043.3(BRIP1):c.270C>A (p.Cys90Ter)	rs1060501740

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