List of variants reported as uncertain significance for Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements by New York Genome Center

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000718.4(CACNA1B):c.5455G>A (p.Ala1819Thr)	rs200122209	0.00039
NM_000718.4(CACNA1B):c.6260C>T (p.Pro2087Leu)	rs200308291	0.00019
NM_000718.4(CACNA1B):c.3421C>T (p.Arg1141Cys)	rs780732725	0.00005
NM_000718.4(CACNA1B):c.2593G>A (p.Asp865Asn)	rs1958874060	0.00001
NM_000718.4(CACNA1B):c.3481G>A (p.Ala1161Thr)	rs200326973	0.00001
NM_000718.4(CACNA1B):c.6323G>A (p.Arg2108Gln)	rs1325101942	0.00001
NM_000718.4(CACNA1B):c.3013G>A (p.Glu1005Lys)	rs1324362568
NM_000718.4(CACNA1B):c.4601C>T (p.Ala1534Val)	rs2133507643
NM_000718.4(CACNA1B):c.79G>T (p.Gly27Cys)	rs758563303

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