"Ambry Genetics"[submitter] AND "ZP3"[gene] - ClinVar

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Items: 54

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2249141	NM_080744.2(SSC4D):c.712G>C (p.Ala238Pro)	SSC4D, ZP3 (A238P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249140	NM_080744.2(SSC4D):c.709G>C (p.Ala237Pro)	SSC4D, ZP3 (A237P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222744	NM_080744.2(SSC4D):c.707T>G (p.Met236Arg)	SSC4D, ZP3 (M236R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408420	NM_080744.2(SSC4D):c.698G>A (p.Gly233Glu)	LOC129998700, SSC4D +1 more (G233E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486570	NM_080744.2(SSC4D):c.671C>G (p.Ala224Gly)	LOC129998700, SSC4D +1 more (A224G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607660	NM_080744.2(SSC4D):c.539T>C (p.Leu180Pro)	SSC4D, ZP3 (L180P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2258516	NM_080744.2(SSC4D):c.419G>A (p.Arg140His)	SSC4D, ZP3 (R140H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324968	NM_080744.2(SSC4D):c.356C>T (p.Pro119Leu)	SSC4D, ZP3 (P119L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269974	NM_080744.2(SSC4D):c.341G>T (p.Gly114Val)	SSC4D, ZP3 (G114V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460770	NM_080744.2(SSC4D):c.322C>T (p.Pro108Ser)	SSC4D, ZP3 (P108S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234217	NM_080744.2(SSC4D):c.319G>A (p.Val107Met)	SSC4D, ZP3 (V107M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616798	NM_080744.2(SSC4D):c.243C>A (p.Ser81Arg)	SSC4D, ZP3 (S81R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170316	NM_080744.2(SSC4D):c.222G>A (p.Met74Ile)	SSC4D, ZP3 (M74I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599488	NM_080744.2(SSC4D):c.79G>A (p.Ala27Thr)	SSC4D, ZP3 (A27T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2320448	NM_080744.2(SSC4D):c.63G>T (p.Arg21Ser)	SSC4D, ZP3 (R21S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491072	NM_080744.2(SSC4D):c.56G>T (p.Gly19Val)	SSC4D, ZP3 (G19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170317	NM_080744.2(SSC4D):c.54G>C (p.Trp18Cys)	SSC4D, ZP3 (W18C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216085	NM_001110354.2(ZP3):c.4G>A (p.Glu2Lys)	ZP3 (E2K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216086	NM_001110354.2(ZP3):c.5A>T (p.Glu2Val)	ZP3 (E2V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357087	NM_001110354.2(ZP3):c.13T>G (p.Tyr5Asp)	ZP3 (Y5D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294499	NM_001110354.2(ZP3):c.38T>C (p.Leu13Pro)	ZP3 (L13P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483826	NM_001110354.2(ZP3):c.44G>A (p.Gly15Asp)	ZP3 (G15D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371431	NM_001110354.2(ZP3):c.70C>T (p.Pro24Ser)	ZP3 (P24S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524579	NM_001110354.2(ZP3):c.110C>T (p.Thr37Met)	ZP3 (T37M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226130	NM_001110354.2(ZP3):c.137G>A (p.Cys46Tyr)	ZP3 (C46Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259985	NM_001110354.2(ZP3):c.280G>A (p.Val94Ile)	ZP3 (V43I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319336	NM_001110354.2(ZP3):c.305G>A (p.Ser102Asn)	ZP3 (S102N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199230	NM_001110354.2(ZP3):c.308T>G (p.Met103Arg)	ZP3 (M52R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611682	NM_001110354.2(ZP3):c.367G>A (p.Val123Met)	ZP3 (V123M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287647	NM_001110354.2(ZP3):c.382A>G (p.Ile128Val)	ZP3 (I128V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259983	NM_001110354.2(ZP3):c.398G>A (p.Arg133His)	ZP3 (R82H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548511	NM_001110354.2(ZP3):c.398G>T (p.Arg133Leu)	ZP3 (R133L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521342	NM_001110354.2(ZP3):c.409C>G (p.Pro137Ala)	ZP3 (P86A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283311	NM_001110354.2(ZP3):c.422G>T (p.Arg141Leu)	ZP3 (R90L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259981	NM_001110354.2(ZP3):c.496T>G (p.Ser166Ala)	ZP3 (S115A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249150	NM_001110354.2(ZP3):c.547G>T (p.Ala183Ser)	ZP3 (A132S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597779	NM_001110354.2(ZP3):c.586G>A (p.Ala196Thr)	ZP3 (A196T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518482	NM_001110354.2(ZP3):c.623T>C (p.Val208Ala)	ZP3 (V208A +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2283265	NM_001110354.2(ZP3):c.779C>T (p.Thr260Ile)	ZP3 (T260I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388595	NM_001110354.2(ZP3):c.791C>A (p.Thr264Lys)	ZP3 (T264K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390116	NM_001110354.2(ZP3):c.798T>A (p.Asp266Glu)	ZP3 (D266E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390117	NM_001110354.2(ZP3):c.800T>A (p.Val267Asp)	ZP3 (V216D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390118	NM_001110354.2(ZP3):c.802T>A (p.Phe268Ile)	ZP3 (F217I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259982	NM_001110354.2(ZP3):c.835T>C (p.Tyr279His)	ZP3 (Y279H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259986	NM_001110354.2(ZP3):c.853A>G (p.Lys285Glu)	ZP3 (K234E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220121	NM_001110354.2(ZP3):c.878C>G (p.Pro293Arg)	ZP3 (P242R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516482	NM_001110354.2(ZP3):c.973G>A (p.Gly325Ser)	ZP3 (G325S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391671	NM_001110354.2(ZP3):c.988C>T (p.Pro330Ser)	ZP3 (P279S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333100	NM_001110354.2(ZP3):c.1045C>T (p.Arg349Cys)	ZP3 (R349C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319104	NM_001110354.2(ZP3):c.1097T>A (p.Ile366Asn)	ZP3 (I315N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199228	NM_001110354.2(ZP3):c.1139C>T (p.Ala380Val)	ZP3 (A380V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510844	NM_001110354.2(ZP3):c.1145C>T (p.Pro382Leu)	ZP3 (P382L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199229	NM_001110354.2(ZP3):c.1163T>A (p.Val388Glu)	ZP3 (V337E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271943	NM_001110354.2(ZP3):c.1240C>T (p.Arg414Cys)	ZP3 (R414C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

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Items: 54