C5394354[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1209726	NM_001042475.3(CEP85L):c.751C>A (p.Pro251Thr)	CEP85L (P251T +1 more)	Single nucleotide variant (missense variant)	Lissencephaly 10	GBenign
Select item 1209727	NM_001042475.3(CEP85L):c.409A>G (p.Ser137Gly)	CEP85L (S137G +1 more)	Single nucleotide variant (missense variant)	Lissencephaly 10	GBenign
Select item 1209728	NM_001042475.3(CEP85L):c.-9T>C	CEP85L, LOC129997071	Single nucleotide variant (5 prime UTR variant +1 more)	Lissencephaly 10	GBenign

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