List of variants reported as uncertain significance by Genomic Center, National Cancer Institute

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.339T>A (p.Asp113Glu)	rs773771416	0.00001
NM_001903.5(CTNNA1):c.1229A>G (p.Asn410Ser)	rs2150032599
NM_001903.5(CTNNA1):c.1392del (p.Ile465fs)	rs2150233636
NM_001903.5(CTNNA1):c.1597A>G (p.Lys533Glu)	rs2150288180
NM_001903.5(CTNNA1):c.163T>C (p.Ser55Pro)	rs1755329623
NM_001903.5(CTNNA1):c.1645del (p.Ala549fs)	rs2150288925
NM_001903.5(CTNNA1):c.1715T>C (p.Val572Ala)	rs2150289732
NM_001903.5(CTNNA1):c.1944del (p.Phe648fs)	rs2150324882
NM_001903.5(CTNNA1):c.2047A>G (p.Lys683Glu)	rs2150334086
NM_001903.5(CTNNA1):c.2470A>G (p.Asn824Asp)	rs2150358511
NM_001903.5(CTNNA1):c.2665A>G (p.Lys889Glu)	rs1766015674
NM_007294.4(BRCA1):c.302-5del	rs2154550280
NM_007294.4(BRCA1):c.4983A>G (p.Glu1661=)	rs2052354666
NM_007294.4(BRCA1):c.5232A>G (p.Arg1744=)	rs2051514714
NM_007294.4(BRCA1):c.5461T>C (p.Phe1821Leu)	rs2050978032

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