"Fulgent Genetics, Fulgent Genetics"[submitter] AND "PCK1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1600211	NM_002591.4(PCK1):c.611-16G>A	PCK1	Single nucleotide variant (intron variant)	Phosphoenolpyruvate carboxykinase deficiency, cytosolic +1 more	GBenign/Likely benign
Select item 338894	NM_002591.4(PCK1):c.1674C>T (p.Ile558=)	PCK1	Single nucleotide variant (synonymous variant)	Phosphoenolpyruvate carboxykinase deficiency, cytosolic +1 more	GBenign/Likely benign