C4748540[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2582433	NM_001282597.3(CTNNA2):c.718del (p.Arg240fs)	CTNNA2 (R240fs +1 more)	Deletion (frameshift variant)	Cortical dysplasia, complex, with other brain malformations 9	GLikely pathogenic
Select item 1027783	NM_001282597.3(CTNNA2):c.1450G>A (p.Val484Ile)	CTNNA2 (V484I +3 more)	Single nucleotide variant (missense variant)	Cortical dysplasia, complex, with other brain malformations 9	GUncertain significance