List of variants reported as uncertain significance for breast carcinoma by Illumina Laboratory Services, Illumina

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1977A>G (p.Arg659=)	rs147215925	0.00230
NM_000465.4(BARD1):c.346C>T (p.His116Tyr)	rs144856889	0.00029
NM_000465.4(BARD1):c.842C>T (p.Pro281Leu)	rs367890377	0.00021
NM_000465.4(BARD1):c.2082C>T (p.Leu694=)	rs139620052	0.00018
NM_000465.4(BARD1):c.279A>G (p.Gln93=)	rs370000575	0.00014
NM_000465.4(BARD1):c.659T>C (p.Leu220Ser)	rs138593305	0.00013
NM_000465.4(BARD1):c.1152C>T (p.Ser384=)	rs368291318	0.00012
NM_000465.4(BARD1):c.1568+15G>T	rs145936354	0.00010
NM_000465.4(BARD1):c.-114A>G	rs778519204	0.00006
NM_000465.4(BARD1):c.1793C>A (p.Thr598Asn)	rs376256852	0.00006
NM_000465.4(BARD1):c.1568T>C (p.Val523Ala)	rs587780017	0.00005
NM_000465.4(BARD1):c.*38C>T	rs751500588	0.00004
NM_000465.4(BARD1):c.1473G>A (p.Gly491=)	rs151080730	0.00004
NM_000465.4(BARD1):c.2280G>A (p.Ser760=)	rs749959440	0.00004
NM_000465.4(BARD1):c.783A>G (p.Leu261=)	rs201862973	0.00004
NM_000465.4(BARD1):c.1915T>C (p.Cys639Arg)	rs587781376	0.00003
NM_000465.4(BARD1):c.2252G>A (p.Arg751Gln)	rs587782246	0.00003
NM_000465.4(BARD1):c.-26G>A	rs1245329214	0.00001
NM_000465.4(BARD1):c.1159T>C (p.Phe387Leu)	rs759370463	0.00001
NM_000465.4(BARD1):c.123C>A (p.Leu41=)	rs764410072	0.00001
NM_000465.4(BARD1):c.382C>T (p.Pro128Ser)	rs878854011	0.00001
NM_000465.4(BARD1):c.465A>G (p.Arg155=)	rs730881413	0.00001
NM_000465.4(BARD1):c.735A>G (p.Gln245=)	rs763378916	0.00001
NM_000465.4(BARD1):c.928T>G (p.Ser310Ala)	rs886041139	0.00001
NM_000465.4(BARD1):c.1147A>T (p.Met383Leu)	rs761516178
NM_000465.4(BARD1):c.215+13G>A	rs886055601
NM_000465.4(BARD1):c.216-14T>C	rs775103922
NM_000465.4(BARD1):c.2189A>C (p.Gln730Pro)	rs876658253
NM_000465.4(BARD1):c.45C>A (p.Arg15=)	rs786201402
NM_000465.4(BARD1):c.587A>G (p.Lys196Arg)	rs587781520
NM_000465.4(BARD1):c.903G>A (p.Glu301=)	rs1694982551
NM_000465.4(BARD1):c.93C>G (p.Arg31=)	rs778803692
NM_000465.4(BARD1):c.98C>T (p.Ala33Val)	rs1559454402

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