List of variants reported as uncertain significance for Cerebrooculofacioskeletal syndrome 3 by Baylor Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000123.4(ERCC5):c.1789G>C (p.Val597Leu)	rs4150319	0.00158
NM_000123.4(ERCC5):c.1768G>A (p.Val590Ile)	rs4150318	0.00108
NM_000123.4(ERCC5):c.56C>T (p.Pro19Leu)	rs34291397	0.00059
NM_000123.4(ERCC5):c.3554A>C (p.Lys1185Thr)	rs201911663	0.00022
NM_000123.4(ERCC5):c.442C>T (p.Pro148Ser)	rs778333931	0.00020
NM_000123.4(ERCC5):c.3038A>G (p.Gln1013Arg)	rs587778292	0.00011
NM_000123.4(ERCC5):c.529-3C>T	rs372122917	0.00008
NM_000123.4(ERCC5):c.1195G>A (p.Glu399Lys)	rs4150315	0.00006
NM_000123.4(ERCC5):c.1460C>T (p.Pro487Leu)	rs560626350	0.00003
NM_000123.4(ERCC5):c.844G>A (p.Val282Ile)	rs747651424	0.00003
NM_000123.4(ERCC5):c.2437A>G (p.Ile813Val)	rs768296301	0.00001
NM_000123.4(ERCC5):c.1339G>A (p.Ala447Thr)	rs2140527689
NM_000123.4(ERCC5):c.2487_2489del (p.Asn829del)	rs1882858341
NM_000123.4(ERCC5):c.3438C>A (p.Ser1146Arg)	rs770177920
NM_000123.4(ERCC5):c.511C>A (p.Gln171Lys)	rs762256976

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