List of variants reported as uncertain significance for Fanconi anemia complementation group J by Revvity Omics, Revvity

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	rs28903098	0.00024
NM_032043.3(BRIP1):c.1629-3T>C	rs587780828	0.00006
NM_032043.3(BRIP1):c.2087C>T (p.Pro696Leu)	rs147755155	0.00006
NM_032043.3(BRIP1):c.689C>T (p.Ser230Leu)	rs759031349	0.00006
NM_032043.3(BRIP1):c.2830C>G (p.Gln944Glu)	rs140233356	0.00003
NM_032043.3(BRIP1):c.2804T>G (p.Val935Gly)	rs4988356	0.00002
NM_032043.3(BRIP1):c.1195G>A (p.Glu399Lys)	rs587782816	0.00001
NM_032043.3(BRIP1):c.1628+5G>A	rs754929230
NM_032043.3(BRIP1):c.1676C>G (p.Thr559Arg)	rs876658266
NM_032043.3(BRIP1):c.1825A>G (p.Thr609Ala)	rs189758577
NM_032043.3(BRIP1):c.2741T>C (p.Leu914Ser)	rs886053215
NM_032043.3(BRIP1):c.3020C>A (p.Ser1007Tyr)	rs886053214
NM_032043.3(BRIP1):c.626A>G (p.Lys209Arg)	rs748912293

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