ZC3H18[gene] and "single gene"[properties] - ClinVar

Search results

Items: 86

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2227144	NM_144604.4(ZC3H18):c.43G>A (p.Glu15Lys)	ZC3H18 (E15K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455128	NM_144604.4(ZC3H18):c.70T>C (p.Ser24Pro)	ZC3H18 (S24P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607575	NM_144604.4(ZC3H18):c.76G>A (p.Asp26Asn)	ZC3H18 (D26N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345400	NM_144604.4(ZC3H18):c.89G>C (p.Arg30Thr)	ZC3H18 (R30T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782142	NM_144604.4(ZC3H18):c.102C>T (p.Ser34=)	ZC3H18	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2374113	NM_144604.4(ZC3H18):c.103G>A (p.Asp35Asn)	ZC3H18 (D35N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512327	NM_144604.4(ZC3H18):c.105T>G (p.Asp35Glu)	ZC3H18 (D35E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2351597	NM_144604.4(ZC3H18):c.164C>T (p.Ala55Val)	ZC3H18 (A55V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302081	NM_144604.4(ZC3H18):c.173C>T (p.Pro58Leu)	ZC3H18 (P58L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 713960	NM_144604.4(ZC3H18):c.196C>T (p.His66Tyr)	ZC3H18 (H66Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2271566	NM_144604.4(ZC3H18):c.205G>A (p.Glu69Lys)	ZC3H18 (E69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334063	NM_144604.4(ZC3H18):c.214C>T (p.Arg72Trp)	ZC3H18 (R72W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236567	NM_144604.4(ZC3H18):c.214C>G (p.Arg72Gly)	ZC3H18 (R72G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374934	NM_144604.4(ZC3H18):c.269G>A (p.Arg90Gln)	ZC3H18 (R90Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310824	NM_144604.4(ZC3H18):c.301G>A (p.Gly101Arg)	ZC3H18 (G101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294385	NM_144604.4(ZC3H18):c.331G>A (p.Asp111Asn)	ZC3H18 (D111N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528759	NM_144604.4(ZC3H18):c.462T>G (p.Asp154Glu)	ZC3H18 (D154E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623745	NM_144604.4(ZC3H18):c.494A>T (p.Glu165Val)	ZC3H18 (E165V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334066	NM_144604.4(ZC3H18):c.511G>A (p.Val171Ile)	ZC3H18 (V171I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192351	NM_144604.4(ZC3H18):c.571G>A (p.Asp191Asn)	ZC3H18 (D191N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227258	NM_144604.4(ZC3H18):c.826G>A (p.Ala276Thr)	ZC3H18 (A300T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479763	NM_144604.4(ZC3H18):c.874C>G (p.Pro292Ala)	ZC3H18 (P316A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555645	NM_144604.4(ZC3H18):c.887C>T (p.Pro296Leu)	ZC3H18 (P296L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359780	NM_144604.4(ZC3H18):c.1014A>C (p.Glu338Asp)	ZC3H18 (E338D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547905	NM_144604.4(ZC3H18):c.1064T>C (p.Ile355Thr)	ZC3H18 (I379T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285472	NM_144604.4(ZC3H18):c.1081G>A (p.Asp361Asn)	ZC3H18 (D385N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192331	NM_144604.4(ZC3H18):c.1090C>T (p.Leu364Phe)	ZC3H18 (L364F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646979	NM_144604.4(ZC3H18):c.1245C>T (p.Arg415=)	ZC3H18	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2483519	NM_144604.4(ZC3H18):c.1316A>C (p.Glu439Ala)	ZC3H18 (E439A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322483	NM_144604.4(ZC3H18):c.1349A>C (p.Lys450Thr)	ZC3H18 (K450T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192332	NM_144604.4(ZC3H18):c.1364G>A (p.Arg455His)	ZC3H18 (R455H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192333	NM_144604.4(ZC3H18):c.1381G>A (p.Asp461Asn)	ZC3H18 (D461N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192334	NM_144604.4(ZC3H18):c.1414C>T (p.Arg472Trp)	ZC3H18 (R472W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192335	NM_144604.4(ZC3H18):c.1450A>C (p.Lys484Gln)	ZC3H18 (K484Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192336	NM_144604.4(ZC3H18):c.1451A>G (p.Lys484Arg)	ZC3H18 (K508R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334069	NM_144604.4(ZC3H18):c.1469C>T (p.Pro490Leu)	ZC3H18 (P514L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405030	NM_144604.4(ZC3H18):c.1477C>T (p.Arg493Cys)	ZC3H18 (R517C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255111	NM_144604.4(ZC3H18):c.1501G>A (p.Glu501Lys)	ZC3H18 (E525K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192337	NM_144604.4(ZC3H18):c.1595C>T (p.Ser532Leu)	ZC3H18 (S532L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478016	NM_144604.4(ZC3H18):c.1598T>C (p.Val533Ala)	ZC3H18 (V533A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589594	NM_144604.4(ZC3H18):c.1604C>T (p.Pro535Leu)	ZC3H18 (P559L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600626	NM_144604.4(ZC3H18):c.1610G>A (p.Arg537Gln)	ZC3H18 (R537Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192338	NM_144604.4(ZC3H18):c.1622G>A (p.Arg541His)	ZC3H18 (R541H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465215	NM_144604.4(ZC3H18):c.1676C>T (p.Ser559Leu)	ZC3H18 (S583L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325135	NM_144604.4(ZC3H18):c.1688C>G (p.Ser563Cys)	ZC3H18 (S587C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334062	NM_144604.4(ZC3H18):c.1702G>A (p.Gly568Ser)	ZC3H18 (G592S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192339	NM_144604.4(ZC3H18):c.1723C>G (p.Arg575Gly)	ZC3H18 (R599G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334068	NM_144604.4(ZC3H18):c.1785C>G (p.Ser595Arg)	ZC3H18 (S595R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510087	NM_144604.4(ZC3H18):c.1811C>T (p.Ser604Leu)	ZC3H18 (S628L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296677	NM_144604.4(ZC3H18):c.1823C>T (p.Pro608Leu)	ZC3H18 (P608L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646980	NM_144604.4(ZC3H18):c.1824G>A (p.Pro608=)	ZC3H18	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3192340	NM_144604.4(ZC3H18):c.1874C>T (p.Pro625Leu)	ZC3H18 (P649L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192341	NM_144604.4(ZC3H18):c.1883C>T (p.Pro628Leu)	ZC3H18 (P628L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334064	NM_144604.4(ZC3H18):c.1895C>T (p.Ala632Val)	ZC3H18 (A632V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192342	NM_144604.4(ZC3H18):c.1909G>C (p.Val637Leu)	ZC3H18 (V637L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2218468	NM_144604.4(ZC3H18):c.1924C>G (p.Pro642Ala)	ZC3H18 (P666A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397957	NM_144604.4(ZC3H18):c.1925C>T (p.Pro642Leu)	ZC3H18 (P642L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2482585	NM_144604.4(ZC3H18):c.1957A>G (p.Thr653Ala)	ZC3H18 (T653A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454251	NM_144604.4(ZC3H18):c.1985C>T (p.Pro662Leu)	ZC3H18 (P686L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557990	NM_144604.4(ZC3H18):c.2035C>T (p.Pro679Ser)	ZC3H18 (P679S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646981	NM_144604.4(ZC3H18):c.2049G>A (p.Thr683=)	ZC3H18	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3192343	NM_144604.4(ZC3H18):c.2119G>A (p.Val707Met)	ZC3H18 (V731M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391687	NM_144604.4(ZC3H18):c.2167G>A (p.Ala723Thr)	ZC3H18 (A723T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334065	NM_144604.4(ZC3H18):c.2188G>C (p.Asp730His)	ZC3H18 (D730H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335000	NM_144604.4(ZC3H18):c.2213C>A (p.Pro738His)	ZC3H18 (P762H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543187	NM_144604.4(ZC3H18):c.2239C>A (p.Pro747Thr)	ZC3H18 (P771T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353030	NM_144604.4(ZC3H18):c.2240C>T (p.Pro747Leu)	ZC3H18 (P771L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362892	NM_144604.4(ZC3H18):c.2258G>T (p.Arg753Met)	ZC3H18 (R777M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479342	NM_144604.4(ZC3H18):c.2274A>T (p.Lys758Asn)	ZC3H18 (K782N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463779	NM_144604.4(ZC3H18):c.2309G>A (p.Arg770Gln)	ZC3H18 (R770Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192345	NM_144604.4(ZC3H18):c.2360G>T (p.Gly787Val)	ZC3H18 (G787V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192346	NM_144604.4(ZC3H18):c.2369C>T (p.Ser790Phe)	ZC3H18 (S790F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207065	NM_144604.4(ZC3H18):c.2387C>T (p.Thr796Ile)	ZC3H18 (T820I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192347	NM_144604.4(ZC3H18):c.2392C>G (p.Gln798Glu)	ZC3H18 (Q798E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481836	NM_144604.4(ZC3H18):c.2407G>A (p.Gly803Arg)	ZC3H18 (G803R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292031	NM_144604.4(ZC3H18):c.2450A>G (p.Lys817Arg)	ZC3H18 (K817R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238640	NM_144604.4(ZC3H18):c.2511C>A (p.Asp837Glu)	ZC3H18 (D837E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606340	NM_144604.4(ZC3H18):c.2518A>T (p.Arg840Trp)	ZC3H18 (R840W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252849	NM_144604.4(ZC3H18):c.2545C>T (p.Pro849Ser)	ZC3H18 (P873S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192348	NM_144604.4(ZC3H18):c.2552C>G (p.Thr851Arg)	ZC3H18 (T851R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192349	NM_144604.4(ZC3H18):c.2572C>T (p.Arg858Trp)	ZC3H18 (R882W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596330	NM_144604.4(ZC3H18):c.2579G>A (p.Arg860Gln)	ZC3H18 (R884Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192350	NM_144604.4(ZC3H18):c.2606C>T (p.Pro869Leu)	ZC3H18 (P893L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515094	NM_144604.4(ZC3H18):c.2618G>A (p.Arg873Gln)	ZC3H18 (R897Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282895	NM_144604.4(ZC3H18):c.2627G>A (p.Gly876Asp)	ZC3H18 (G876D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383185	NM_144604.4(ZC3H18):c.2743G>A (p.Ala915Thr)	ZC3H18 (A939T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 86