List of variants reported as uncertain significance for Developmental and epileptic encephalopathy, 42 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6527G>T (p.Gly2176Val)	rs763045560	0.00008
NM_001127222.2(CACNA1A):c.1213G>A (p.Ala405Thr)	rs121908245	0.00001
NM_001127222.2(CACNA1A):c.7318G>A (p.Val2440Ile)	rs765880617	0.00001
NM_001127222.2(CACNA1A):c.1106G>A (p.Arg369Gln)	rs2513049253
NM_001127222.2(CACNA1A):c.3652C>T (p.Pro1218Ser)	rs2512848352
NM_001127222.2(CACNA1A):c.4328A>G (p.Asp1443Gly)	rs2056674575
NM_001127222.2(CACNA1A):c.6862del (p.Gln2288fs)	rs2144493067

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