C3810407[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1213605	NM_001069.3(TUBB2A):c.967A>C (p.Met323Leu)	TUBB2A (M238L +1 more)	Single nucleotide variant (missense variant)	Complex cortical dysplasia with other brain malformations 5 +1 more	GLikely pathogenic
Select item 975997	NM_001069.3(TUBB2A):c.292G>C (p.Gly98Arg)	TUBB2A (G13R +1 more)	Single nucleotide variant (missense variant)	Complex cortical dysplasia with other brain malformations 5 +1 more	GPathogenic/Likely pathogenic