"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CTDP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 777336	NM_004715.5(CTDP1):c.492+7C>T	CTDP1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1163617	NM_004715.5(CTDP1):c.1219T>C (p.Trp407Arg)	CTDP1 (W288R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 769941	NM_004715.5(CTDP1):c.2070C>T (p.Gly690=)	CTDP1	Single nucleotide variant (synonymous variant)	Congenital cataracts-facial dysmorphism-neuropathy syndrome +1 more	GBenign/Likely benign

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