"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FYCO1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 468446	NM_024513.4(FYCO1):c.3779C>G (p.Pro1260Arg)	FYCO1 (P1260R)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 468445	NM_024513.4(FYCO1):c.2857G>T (p.Gly953Trp)	FYCO1 (G953W)	Single nucleotide variant (missense variant)	Cataract 18	GUncertain significance
Select item 468439	NM_024513.4(FYCO1):c.1439C>T (p.Thr480Met)	FYCO1 (T480M)	Single nucleotide variant (missense variant)	FYCO1-related disorder +2 more	GBenign/Likely benign

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