"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CACNA1B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 716987	NM_000718.4(CACNA1B):c.2581C>T (p.Pro861Ser)	CACNA1B (P861S)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements +1 more	GBenign/Likely benign
Select item 1659909	NM_000718.4(CACNA1B):c.2886C>A (p.Pro962=)	CACNA1B	Single nucleotide variant (synonymous variant)	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements +1 more	GLikely benign
Select item 719151	NM_000718.4(CACNA1B):c.3279C>T (p.Val1093=)	CACNA1B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 718024	NM_000718.4(CACNA1B):c.3673A>G (p.Ile1225Val)	CACNA1B (I1225V)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements +1 more	GBenign
Select item 784513	NM_000718.4(CACNA1B):c.5649+9C>A	CACNA1B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1571488	NM_000718.4(CACNA1B):c.6072G>A (p.Thr2024=)	CACNA1B	Single nucleotide variant (synonymous variant)	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements +1 more	GBenign

ClinVar