C3809013[trait identifier] AND "Institute of Human Genetics, Cologne U - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638268	NM_004522.3(KIF5C):c.1018G>A (p.Glu340Lys)	KIF5C (E340K)	Single nucleotide variant (missense variant +1 more)	Complex cortical dysplasia with other brain malformations 2	GLikely benign
Select item 638267	NM_004522.3(KIF5C):c.1864A>G (p.Ser622Gly)	KIF5C (S622G)	Single nucleotide variant (missense variant +1 more)	Complex cortical dysplasia with other brain malformations 2	GUncertain significance