ZNF23[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2347040	NM_001381984.1(ZNF23):c.1898G>A (p.Cys633Tyr)	ZNF23 (C532Y +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605935	NM_001381984.1(ZNF23):c.1882G>A (p.Glu628Lys)	ZNF23 (E585K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318173	NM_001381984.1(ZNF23):c.1858C>T (p.Arg620Trp)	ZNF23 (R577W +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335214	NM_001381984.1(ZNF23):c.1793C>T (p.Thr598Ile)	ZNF23 (T593I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539404	NM_001381984.1(ZNF23):c.1769A>C (p.Tyr590Ser)	ZNF23 (Y586S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549403	NM_001381984.1(ZNF23):c.1742A>C (p.Glu581Ala)	ZNF23 (E538A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335211	NM_001381984.1(ZNF23):c.1724T>G (p.Phe575Cys)	ZNF23 (F532C +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270355	NM_001381984.1(ZNF23):c.1661A>G (p.Lys554Arg)	ZNF23 (K549R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194556	NM_001381984.1(ZNF23):c.1616G>A (p.Arg539Gln)	ZNF23 (R500Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529818	NM_001381984.1(ZNF23):c.1603C>G (p.Leu535Val)	ZNF23 (L434V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568568	NM_001381984.1(ZNF23):c.1571G>A (p.Cys524Tyr)	ZNF23 (C485Y +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521286	NM_001381984.1(ZNF23):c.1544G>C (p.Gly515Ala)	ZNF23 (G414A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335212	NM_001381984.1(ZNF23):c.1541C>G (p.Thr514Ser)	ZNF23 (T510S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194555	NM_001381984.1(ZNF23):c.1523G>A (p.Arg508Gln)	ZNF23 (R407Q +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2590804	NM_001381984.1(ZNF23):c.1522C>T (p.Arg508Trp)	ZNF23 (R465W +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521285	NM_001381984.1(ZNF23):c.1520T>C (p.Met507Thr)	ZNF23 (M465T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262193	NM_001381984.1(ZNF23):c.1493A>G (p.Lys498Arg)	ZNF23 (K455R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194554	NM_001381984.1(ZNF23):c.1421G>A (p.Cys474Tyr)	ZNF23 (C432Y +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306654	NM_001381984.1(ZNF23):c.1220A>G (p.Tyr407Cys)	ZNF23 (Y368C +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335213	NM_001381984.1(ZNF23):c.1210G>C (p.Glu404Gln)	ZNF23 (E365Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247980	NM_001381984.1(ZNF23):c.1160G>C (p.Gly387Ala)	ZNF23 (G286A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319650	NM_001381984.1(ZNF23):c.1035C>G (p.His345Gln)	ZNF23 (H306Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382019	NM_001381984.1(ZNF23):c.953C>T (p.Thr318Met)	ZNF23 (T217M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401177	NM_001381984.1(ZNF23):c.913A>G (p.Ser305Gly)	ZNF23 (S263G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475991	NM_001381984.1(ZNF23):c.785G>A (p.Ser262Asn)	ZNF23 (S219N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470563	NM_001381984.1(ZNF23):c.698A>C (p.Asn233Thr)	ZNF23 (N190T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542918	NM_001381984.1(ZNF23):c.584A>G (p.Asp195Gly)	ZNF23 (D156G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194558	NM_001381984.1(ZNF23):c.474C>A (p.Ser158Arg)	ZNF23 (S116R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478891	NM_001381984.1(ZNF23):c.379T>C (p.Ser127Pro)	ZNF23 (S122P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492276	NM_001381984.1(ZNF23):c.301G>A (p.Glu101Lys)	ZNF23 (E101K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194557	NM_001381984.1(ZNF23):c.287A>G (p.Asn96Ser)	ZNF23 (N91S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287039	NM_001381984.1(ZNF23):c.224C>T (p.Ser75Leu)	ZNF23 (S75L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 32