List of variants reported as uncertain significance for Microcephaly 5, primary, autosomal recessive by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.7114A>G (p.Arg2372Gly)	rs190693455	0.00021
NM_018136.5(ASPM):c.8452G>T (p.Ala2818Ser)	rs188955444	0.00021
NM_018136.5(ASPM):c.5510G>A (p.Gly1837Asp)	rs144969324	0.00011
NM_018136.5(ASPM):c.2824C>T (p.Arg942Cys)	rs546095187	0.00004
NM_018136.5(ASPM):c.2629+3A>G	rs758509567	0.00002
NM_018136.5(ASPM):c.3232A>T (p.Ser1078Cys)
NM_018136.5(ASPM):c.5600C>A (p.Thr1867Lys)
NM_018136.5(ASPM):c.7937A>G (p.His2646Arg)
NM_018136.5(ASPM):c.8615C>T (p.Thr2872Met)

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