"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CDT1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 434673	NM_030928.4(CDT1):c.613G>A (p.Gly205Ser)	CDT1 (G205S)	Single nucleotide variant (missense variant)	Meier-Gorlin syndrome 4 +2 more	GConflicting classifications of pathogenicity
Select item 799874	NM_030928.4(CDT1):c.999G>A (p.Pro333=)	CDT1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 128671	NM_030928.4(CDT1):c.1521G>A (p.Pro507=)	CDT1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign

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