List of variants reported as likely pathogenic by Center for Precision Medicine, Meizhou People's Hospital

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.5096G>A (p.Arg1699Gln)	rs41293459	0.00001
NM_000059.4(BRCA2):c.8331+1G>A	rs81002837
NM_000059.4(BRCA2):c.8954-5A>G	rs886040949
NM_007294.4(BRCA1):c.140G>T (p.Cys47Phe)	rs80357150
NM_007294.4(BRCA1):c.4986+5G>A	rs397509211
NM_007294.4(BRCA1):c.5072C>A (p.Thr1691Lys)	rs80357034
NM_007294.4(BRCA1):c.5194-2A>G	rs80358069
NM_007294.4(BRCA1):c.671-1G>T	rs80358020

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