"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC130064417"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41377	NM_203486.3(DLL3):c.425T>A (p.Leu142Gln)	DLL3, LOC130064417 (L142Q)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 559885	NM_203486.3(DLL3):c.534C>A (p.Cys178Ter)	DLL3, LOC130064417 (C178*)	Single nucleotide variant (nonsense)	Spondylocostal dysostosis 1, autosomal recessive	GLikely pathogenic