"Victorian Clinical Genetics Services, Murdoch Childrens Research Inst - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 591864	NM_005883.3(APC2):c.322_323inv (p.Ser108Leu)	APC2 (S108L)	Inversion (missense variant)	Cortical dysplasia, complex, with other brain malformations 10 +1 more	GUncertain significance
Select item 1805267	NM_005883.3(APC2):c.4531G>A (p.Gly1511Ser)	APC2 (G1510S +1 more)	Single nucleotide variant (missense variant)	Cortical dysplasia, complex, with other brain malformations 10	GUncertain significance