List of variants reported as likely benign for Baraitser-Winter syndrome 1; Developmental malformations-deafness-dystonia syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_001101.5(ACTB):c.426G>T (p.Leu142=)	rs79074016	0.00353
NM_001101.5(ACTB):c.687G>A (p.Thr229=)	rs138499594	0.00083
NM_001101.5(ACTB):c.762G>C (p.Arg254=)	rs145818896	0.00080
NM_001101.5(ACTB):c.1107C>T (p.Ile369=)	rs71531321	0.00065
NM_001101.5(ACTB):c.984+15T>C	rs372551192	0.00039
NM_001101.5(ACTB):c.645G>A (p.Lys215=)	rs145017784	0.00026
NM_001101.5(ACTB):c.364-4A>G	rs763065691	0.00018
NM_001101.5(ACTB):c.315G>C (p.Leu105=)	rs139795454	0.00016
NM_001101.5(ACTB):c.453C>T (p.Ile151=)	rs150837984	0.00012
NM_001101.5(ACTB):c.36C>T (p.Asn12=)	rs764325153	0.00004
NM_001101.5(ACTB):c.1014C>T (p.Ser338=)	rs1064790	0.00003
NM_001101.5(ACTB):c.24C>G (p.Leu8=)	rs151181948	0.00003
NM_001101.5(ACTB):c.267C>T (p.Thr89=)	rs760279394	0.00003
NM_001101.5(ACTB):c.363+15A>C	rs772907450	0.00003
NM_001101.5(ACTB):c.429C>T (p.Tyr143=)	rs375215955	0.00003
NM_001101.5(ACTB):c.858C>T (p.Asp286=)	rs150105166	0.00003
NM_001101.5(ACTB):c.270C>T (p.Phe90=)	rs1446932164	0.00001
NM_001101.5(ACTB):c.364-8C>T	rs751843940	0.00001
NM_001101.5(ACTB):c.474G>A (p.Gly158=)	rs141472083	0.00001
NM_001101.5(ACTB):c.63C>T (p.Phe21=)	rs370972197	0.00001
NM_001101.5(ACTB):c.642G>A (p.Glu214=)	rs769411154	0.00001
NM_001101.5(ACTB):c.882C>T (p.Tyr294=)	rs774758801	0.00001
NM_001101.5(ACTB):c.-6-15C>G	rs375195937
NM_001101.5(ACTB):c.803-7C>T	rs780471227
NM_001101.5(ACTB):c.903C>T (p.Gly301=)	rs13447407

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