ClinVar for Gene (Select 7772) - ClinVar

Links from Gene

Items: 86

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335210	NM_014518.4(ZNF229):c.1652A>G (p.Lys551Arg)	ZNF229 (K545R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335209	NM_014518.4(ZNF229):c.2341T>C (p.Ser781Pro)	ZNF229 (S775P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335208	NM_014518.4(ZNF229):c.1076G>A (p.Arg359Lys)	ZNF229 (R359K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335207	NM_014518.4(ZNF229):c.365G>A (p.Cys122Tyr)	ZNF229 (C116Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335206	NM_014518.4(ZNF229):c.1487A>C (p.Lys496Thr)	ZNF229 (K496T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335205	NM_014518.4(ZNF229):c.770G>A (p.Arg257His)	ZNF229 (R251H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3335204	NM_014518.4(ZNF229):c.473A>G (p.Asp158Gly)	ZNF229 (D158G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335203	NM_014518.4(ZNF229):c.443C>T (p.Thr148Met)	ZNF229 (T148M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335202	NM_014518.4(ZNF229):c.415C>G (p.Pro139Ala)	ZNF229 (P139A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335201	NM_014518.4(ZNF229):c.742G>T (p.Asp248Tyr)	ZNF229 (D242Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335200	NM_014518.4(ZNF229):c.931C>T (p.His311Tyr)	ZNF229 (H305Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194553	NM_014518.4(ZNF229):c.977G>A (p.Arg326His)	ZNF229 (R326H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194552	NM_014518.4(ZNF229):c.901G>A (p.Gly301Ser)	ZNF229 (G301S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194551	NM_014518.4(ZNF229):c.841C>T (p.Pro281Ser)	ZNF229 (P275S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194550	NM_014518.4(ZNF229):c.820T>C (p.Phe274Leu)	ZNF229 (F268L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194549	NM_014518.4(ZNF229):c.775A>G (p.Asn259Asp)	ZNF229 (N253D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194548	NM_014518.4(ZNF229):c.770G>T (p.Arg257Leu)	ZNF229 (R251L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194547	NM_014518.4(ZNF229):c.725G>T (p.Cys242Phe)	ZNF229 (C242F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194546	NM_014518.4(ZNF229):c.547C>T (p.Pro183Ser)	ZNF229 (P177S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194545	NM_014518.4(ZNF229):c.542C>T (p.Pro181Leu)	ZNF229 (P181L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194544	NM_014518.4(ZNF229):c.434G>T (p.Gly145Val)	ZNF229 (G139V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194543	NM_014518.4(ZNF229):c.343G>A (p.Glu115Lys)	ZNF229 (E115K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194542	NM_014518.4(ZNF229):c.305A>G (p.Glu102Gly)	ZNF229 (E96G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194541	NM_014518.4(ZNF229):c.269T>A (p.Ile90Asn)	ZNF229 (I84N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194540	NM_014518.4(ZNF229):c.2371A>T (p.Thr791Ser)	ZNF229 (T791S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194539	NM_014518.4(ZNF229):c.2252A>C (p.Gln751Pro)	ZNF229 (Q745P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194538	NM_014518.4(ZNF229):c.2090C>G (p.Ser697Cys)	ZNF229 (S691C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194537	NM_014518.4(ZNF229):c.1786G>A (p.Gly596Arg)	ZNF229 (G590R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194536	NM_014518.4(ZNF229):c.1423C>T (p.His475Tyr)	ZNF229 (H475Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194535	NM_014518.4(ZNF229):c.1360A>G (p.Ile454Val)	ZNF229 (I448V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3194533	NM_014518.4(ZNF229):c.1228T>C (p.Cys410Arg)	ZNF229 (C410R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194532	NM_014518.4(ZNF229):c.1061G>A (p.Cys354Tyr)	ZNF229 (C348Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194531	NM_014518.4(ZNF229):c.1046A>G (p.Tyr349Cys)	ZNF229 (Y349C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2672773	NM_014518.4(ZNF229):c.1443G>T (p.Lys481Asn)	ZNF229 (K475N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2650082	NM_014518.4(ZNF229):c.2T>C (p.Met1Thr)	ZNF229 (M1T)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2650081	NM_014518.4(ZNF229):c.1744C>T (p.Arg582Trp)	ZNF229 (R576W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2622092	NM_014518.4(ZNF229):c.1153G>T (p.Ala385Ser)	ZNF229 (A379S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596689	NM_014518.4(ZNF229):c.2036C>T (p.Thr679Met)	ZNF229 (T673M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561108	NM_014518.4(ZNF229):c.1849A>G (p.Ile617Val)	ZNF229 (I617V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545243	NM_014518.4(ZNF229):c.1838C>T (p.Ser613Phe)	ZNF229 (S607F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535307	NM_014518.4(ZNF229):c.2098C>A (p.Arg700Ser)	ZNF229 (R694S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525439	NM_014518.4(ZNF229):c.2179C>T (p.Leu727Phe)	ZNF229 (L727F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525175	NM_014518.4(ZNF229):c.454C>A (p.Pro152Thr)	ZNF229 (P152T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523886	NM_014518.4(ZNF229):c.446C>T (p.Pro149Leu)	ZNF229 (P143L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514847	NM_014518.4(ZNF229):c.457A>C (p.Ile153Leu)	ZNF229 (I147L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507463	NM_014518.4(ZNF229):c.2347C>T (p.Leu783Phe)	ZNF229 (L783F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475599	NM_014518.4(ZNF229):c.644G>A (p.Cys215Tyr)	ZNF229 (C215Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475338	NM_014518.4(ZNF229):c.2383C>T (p.Pro795Ser)	ZNF229 (P789S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463771	NM_014518.4(ZNF229):c.830A>T (p.Asp277Val)	ZNF229 (D271V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460469	NM_014518.4(ZNF229):c.115G>A (p.Val39Met)	ZNF229 (V39M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456493	NM_014518.4(ZNF229):c.1085C>T (p.Ser362Leu)	ZNF229 (S356L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	CADM4, CEACAM16 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 2405672	NM_014518.4(ZNF229):c.1489G>A (p.Gly497Ser)	ZNF229 (G491S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2403028	NM_014518.4(ZNF229):c.2390C>T (p.Thr797Met)	ZNF229 (T797M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400761	NM_014518.4(ZNF229):c.2461G>A (p.Glu821Lys)	ZNF229 (E821K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389008	NM_014518.4(ZNF229):c.1390G>T (p.Gly464Cys)	ZNF229 (G464C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383827	NM_014518.4(ZNF229):c.2458G>T (p.Gly820Cys)	ZNF229 (G820C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375732	NM_014518.4(ZNF229):c.1561G>A (p.Val521Met)	ZNF229 (V515M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362751	NM_014518.4(ZNF229):c.1055A>T (p.Asp352Val)	ZNF229 (D346V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361642	NM_014518.4(ZNF229):c.2372C>A (p.Thr791Asn)	ZNF229 (T791N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357412	NM_014518.4(ZNF229):c.2098C>T (p.Arg700Cys)	ZNF229 (R694C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353533	NM_014518.4(ZNF229):c.2252A>G (p.Gln751Arg)	ZNF229 (Q745R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337437	NM_014518.4(ZNF229):c.1963C>T (p.Pro655Ser)	ZNF229 (P655S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316834	NM_014518.4(ZNF229):c.2396G>A (p.Gly799Asp)	ZNF229 (G793D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2305239	NM_014518.4(ZNF229):c.1747C>T (p.Arg583Trp)	ZNF229 (R577W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294992	NM_014518.4(ZNF229):c.2393G>A (p.Cys798Tyr)	ZNF229 (C798Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293840	NM_014518.4(ZNF229):c.204G>C (p.Arg68Ser)	ZNF229 (R68S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285217	NM_014518.4(ZNF229):c.2057G>T (p.Cys686Phe)	ZNF229 (C686F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277027	NM_014518.4(ZNF229):c.344A>T (p.Glu115Val)	ZNF229 (E109V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270365	NM_014518.4(ZNF229):c.1050A>T (p.Arg350Ser)	ZNF229 (R344S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249427	NM_014518.4(ZNF229):c.1801G>A (p.Val601Met)	ZNF229 (V601M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246568	NM_014518.4(ZNF229):c.1043C>T (p.Pro348Leu)	ZNF229 (P348L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2239692	NM_014518.4(ZNF229):c.966G>C (p.Lys322Asn)	ZNF229 (K322N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225325	NM_014518.4(ZNF229):c.1774A>G (p.Arg592Gly)	ZNF229 (R592G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225107	NM_014518.4(ZNF229):c.1672G>A (p.Asp558Asn)	ZNF229 (D552N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211000	NM_014518.4(ZNF229):c.1601T>C (p.Met534Thr)	ZNF229 (M528T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	C5AR1, C5AR2 +293 more	Copy number gain	not provided	GPathogenic
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 546844	NM_014518.4(ZNF229):c.1895A>C (p.Glu632Ala)	ZNF229 (E626A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 442437	GRCh37/hg19 19q13.31-13.32(chr19:44300416-45639540)x1	APOC1, APOC2 +39 more	Copy number loss	See cases	GUncertain significance
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	APOC1, APOC2 +120 more	Copy number loss	See cases	GPathogenic
Select item 221402	GRCh37/hg19 19q13.31(chr19:44466919-45029206)x1	CEACAM20, ZNF112 +16 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221352	chr19:44501518-45322744 complex variant	BCAM, BCL3 +22 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 86