List of variants reported as uncertain significance for Microcephaly 5, primary, autosomal recessive by Baylor Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.5452C>T (p.Arg1818Cys)	rs41299625	0.00095
NM_018136.5(ASPM):c.4214G>A (p.Arg1405His)	rs143092798	0.00016
NM_018136.5(ASPM):c.2365A>G (p.Ile789Val)	rs755203240	0.00011
NM_018136.5(ASPM):c.6131A>G (p.Asn2044Ser)	rs145645602	0.00008
NM_018136.5(ASPM):c.2824C>T (p.Arg942Cys)	rs546095187	0.00004
NM_018136.5(ASPM):c.4457A>G (p.Tyr1486Cys)	rs368020945	0.00004
NM_018136.5(ASPM):c.1931T>A (p.Ile644Lys)	rs759534488	0.00002
NM_018136.5(ASPM):c.1697C>T (p.Ser566Leu)	rs555866170	0.00001
NM_018136.5(ASPM):c.2312G>A (p.Arg771His)	rs375059809	0.00001
NM_018136.5(ASPM):c.3683G>A (p.Gly1228Asp)	rs867611929	0.00001
NM_018136.5(ASPM):c.3725C>T (p.Thr1242Ile)	rs923491109	0.00001
NM_018136.5(ASPM):c.5055G>T (p.Leu1685Phe)	rs768697877	0.00001
NM_018136.5(ASPM):c.3115A>G (p.Arg1039Gly)	rs1259632140
NM_018136.5(ASPM):c.5138G>A (p.Arg1713His)	rs141297873
NM_018136.5(ASPM):c.7966AGA[1] (p.Arg2657del)	rs775391911

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