"Ambry Genetics"[submitter] AND "ZFP1"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2466203	NM_153688.4(ZFP1):c.47A>G (p.Asp16Gly)	ZFP1 (D16G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459656	NM_153688.4(ZFP1):c.83C>G (p.Ser28Cys)	ZFP1 (S28C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2619858	NM_153688.4(ZFP1):c.144A>C (p.Glu48Asp)	ZFP1 (E48D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489076	NM_153688.4(ZFP1):c.163C>A (p.Gln55Lys)	ZFP1 (Q55K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2291218	NM_153688.4(ZFP1):c.224A>G (p.Asn75Ser)	ZFP1 (N42S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400273	NM_153688.4(ZFP1):c.302A>G (p.Gln101Arg)	ZFP1 (Q68R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193079	NM_153688.4(ZFP1):c.329A>G (p.Glu110Gly)	ZFP1 (E110G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484037	NM_153688.4(ZFP1):c.340A>G (p.Lys114Glu)	ZFP1 (K59E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556909	NM_153688.4(ZFP1):c.352G>C (p.Asp118His)	ZFP1 (D63H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487492	NM_153688.4(ZFP1):c.371G>T (p.Arg124Ile)	ZFP1 (R91I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250371	NM_153688.4(ZFP1):c.395A>G (p.Asp132Gly)	ZFP1 (D132G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614231	NM_153688.4(ZFP1):c.449A>G (p.His150Arg)	ZFP1 (H117R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544360	NM_153688.4(ZFP1):c.467C>T (p.Ser156Phe)	ZFP1 (S101F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398334	NM_153688.4(ZFP1):c.479A>G (p.Lys160Arg)	ZFP1 (K105R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334437	NM_153688.4(ZFP1):c.511A>G (p.Ile171Val)	ZFP1 (I138V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556669	NM_153688.4(ZFP1):c.514T>G (p.Phe172Val)	ZFP1 (F117V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334434	NM_153688.4(ZFP1):c.763C>T (p.Leu255Phe)	ZFP1 (L255F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334433	NM_153688.4(ZFP1):c.968G>A (p.Arg323His)	ZFP1 (R323H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334436	NM_153688.4(ZFP1):c.980G>A (p.Ser327Asn)	ZFP1 (S327N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494529	NM_153688.4(ZFP1):c.1034C>T (p.Thr345Ile)	ZFP1 (T345I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334435	NM_153688.4(ZFP1):c.1064C>A (p.Thr355Asn)	ZFP1 (T300N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469845	NM_153688.4(ZFP1):c.1190T>G (p.Val397Gly)	ZFP1 (V342G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378576	NM_153688.4(ZFP1):c.1210G>A (p.Gly404Arg)	ZFP1 (G349R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 23