"Ambry Genetics"[submitter] AND "CNBP"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3268079	NM_003418.5(CNBP):c.461G>C (p.Ser154Thr)	CNBP (S155T +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588404	NM_003418.5(CNBP):c.457A>G (p.Thr153Ala)	CNBP (T154A +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292669	NM_003418.5(CNBP):c.338A>G (p.His113Arg)	CNBP (H107R +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511843	NM_003418.5(CNBP):c.310C>G (p.Pro104Ala)	CNBP (P97A +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146401	NM_003418.5(CNBP):c.299A>G (p.Asn100Ser)	CNBP (N94S +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306192	NM_003418.5(CNBP):c.15G>C (p.Glu5Asp)	CNBP (E5D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar