"Ambry Genetics"[submitter] AND "ZNF419"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2335886	NM_024691.4(ZNF419):c.19A>G (p.Arg7Gly)	ZNF419 (R7G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301782	NM_024691.4(ZNF419):c.88G>C (p.Glu30Gln)	ZNF419 (E17Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527827	NM_024691.4(ZNF419):c.91G>T (p.Asp31Tyr)	ZNF419 (D31Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236967	NM_024691.4(ZNF419):c.155A>C (p.Tyr52Ser)	ZNF419 (Y39S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195643	NM_024691.4(ZNF419):c.166A>G (p.Met56Val)	ZNF419 (M56V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357887	NM_024691.4(ZNF419):c.221A>G (p.His74Arg)	ZNF419 (H61R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517186	NM_024691.4(ZNF419):c.293C>T (p.Pro98Leu)	ZNF419 (P86L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195644	NM_024691.4(ZNF419):c.331C>T (p.Pro111Ser)	ZNF419 (P99S +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286046	NM_024691.4(ZNF419):c.455T>A (p.Val152Asp)	ZNF419 (V120D +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486751	NM_024691.4(ZNF419):c.464C>T (p.Ser155Leu)	ZNF419 (S110L +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300536	NM_024691.4(ZNF419):c.494G>A (p.Gly165Glu)	ZNF419 (G119E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195645	NM_024691.4(ZNF419):c.674A>G (p.His225Arg)	ZNF419 (H180R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365959	NM_024691.4(ZNF419):c.725A>G (p.Asp242Gly)	ZNF419 (D210G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276498	NM_024691.4(ZNF419):c.726T>G (p.Asp242Glu)	ZNF419 (D209E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195646	NM_024691.4(ZNF419):c.787A>G (p.Asn263Asp)	ZNF419 (N230D +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2358464	NM_024691.4(ZNF419):c.808C>T (p.Arg270Cys)	ZNF419 (R238C +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195647	NM_024691.4(ZNF419):c.856C>G (p.Pro286Ala)	ZNF419 (P198A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393476	NM_024691.4(ZNF419):c.880A>G (p.Lys294Glu)	ZNF419 (K281E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489301	NM_024691.4(ZNF419):c.908T>C (p.Val303Ala)	ZNF419 (V304A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392202	NM_024691.4(ZNF419):c.911A>G (p.Gln304Arg)	ZNF419 (Q258R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195648	NM_024691.4(ZNF419):c.940C>A (p.Pro314Thr)	ZNF419 (P268T +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278056	NM_024691.4(ZNF419):c.991A>G (p.Met331Val)	ZNF419 (M285V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610783	NM_024691.4(ZNF419):c.998A>G (p.His333Arg)	ZNF419 (H334R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239494	NM_024691.4(ZNF419):c.1025C>A (p.Pro342His)	ZNF419 (P254H +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195641	NM_024691.4(ZNF419):c.1114A>G (p.Lys372Glu)	ZNF419 (K327E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2376302	NM_024691.4(ZNF419):c.1123G>A (p.Asp375Asn)	ZNF419 (D330N +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241959	NM_024691.4(ZNF419):c.1178A>G (p.His393Arg)	ZNF419 (H361R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456524	NM_024691.4(ZNF419):c.1199A>C (p.Lys400Thr)	ZNF419 (K312T +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329370	NM_024691.4(ZNF419):c.1220T>A (p.Phe407Tyr)	ZNF419 (F362Y +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598270	NM_024691.4(ZNF419):c.1285T>C (p.Cys429Arg)	ZNF419 (C417R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195642	NM_024691.4(ZNF419):c.1462T>C (p.Cys488Arg)	ZNF419 (C400R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370135	NM_024691.4(ZNF419):c.1478G>A (p.Arg493His)	ZNF419 (R405H +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 32