ClinVar for Gene (Select 7620) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259436	NM_001367172.2(ZNF763):c.800G>A (p.Ser267Asn)	ZNF69, ZNF763 (S145N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259435	NM_001367172.2(ZNF763):c.904C>G (p.His302Asp)	ZNF69, ZNF763 (H302D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259434	NM_001367172.2(ZNF763):c.1067G>A (p.Arg356His)	ZNF69, ZNF763 (R234H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259433	NM_001367172.2(ZNF763):c.326T>C (p.Phe109Ser)	ZNF69, ZNF763 (F111S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259270	NM_144566.3(ZNF700):c.101C>A (p.Thr34Asn)	ZNF69, ZNF700 (T37N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259269	NM_144566.3(ZNF700):c.2159A>G (p.His720Arg)	ZNF69, ZNF700 (H720R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259268	NM_144566.3(ZNF700):c.1658A>G (p.Tyr553Cys)	ZNF69, ZNF700 (Y556C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259267	NM_144566.3(ZNF700):c.1028T>C (p.Leu343Ser)	ZNF69, ZNF700 (L346S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259265	NM_144566.3(ZNF700):c.1612T>A (p.Cys538Ser)	ZNF69, ZNF700 (C538S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259264	NM_144566.3(ZNF700):c.1039A>G (p.Ile347Val)	ZNF69, ZNF700 (I350V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259263	NM_144566.3(ZNF700):c.2167G>A (p.Ala723Thr)	ZNF69, ZNF700 (A723T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259262	NM_144566.3(ZNF700):c.1079G>C (p.Arg360Thr)	ZNF69, ZNF700 (R363T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259261	NM_144566.3(ZNF700):c.1066A>C (p.Asn356His)	ZNF69, ZNF700 (N356H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3259212	NM_001364730.1(ZNF69):c.163G>A (p.Glu55Lys)	ZNF69 (E41K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198156	NM_001367172.2(ZNF763):c.737A>T (p.His246Leu)	ZNF69, ZNF763 (H124L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198155	NM_001367172.2(ZNF763):c.731G>A (p.Arg244Gln)	ZNF69, ZNF763 (R247Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3198154	NM_001367172.2(ZNF763):c.403G>C (p.Glu135Gln)	ZNF69, ZNF763 (E137Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198153	NM_001367172.2(ZNF763):c.403G>A (p.Glu135Lys)	ZNF69, ZNF763 (E137K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198152	NM_001367172.2(ZNF763):c.350G>A (p.Gly117Asp)	ZNF69, ZNF763 (G117D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198151	NM_001367172.2(ZNF763):c.183A>T (p.Arg61Ser)	ZNF69, ZNF763 (R63S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198150	NM_001367172.2(ZNF763):c.121A>G (p.Thr41Ala)	ZNF69, ZNF763 (T41A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3197848	NM_144566.3(ZNF700):c.997C>A (p.Pro333Thr)	ZNF69, ZNF700 (P333T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197847	NM_144566.3(ZNF700):c.964C>T (p.Arg322Cys)	ZNF69, ZNF700 (R322C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197846	NM_144566.3(ZNF700):c.941C>T (p.Ala314Val)	ZNF69, ZNF700 (A317V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197845	NM_144566.3(ZNF700):c.875C>G (p.Ser292Cys)	ZNF69, ZNF700 (S292C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197844	NM_144566.3(ZNF700):c.745C>T (p.Pro249Ser)	ZNF69, ZNF700 (P252S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197843	NM_144566.3(ZNF700):c.726A>C (p.Arg242Ser)	ZNF69, ZNF700 (R245S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197842	NM_144566.3(ZNF700):c.37C>T (p.Pro13Ser)	ZNF69, ZNF700 (P13S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197841	NM_144566.3(ZNF700):c.277G>A (p.Glu93Lys)	ZNF69, ZNF700 (E96K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197840	NM_144566.3(ZNF700):c.223G>C (p.Glu75Gln)	ZNF69, ZNF700 (E78Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197839	NM_144566.3(ZNF700):c.2107C>T (p.His703Tyr)	ZNF69, ZNF700 (H703Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197838	NM_144566.3(ZNF700):c.2101G>C (p.Glu701Gln)	ZNF69, ZNF700 (E701Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197837	NM_144566.3(ZNF700):c.1943A>G (p.Tyr648Cys)	ZNF69, ZNF700 (Y651C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197836	NM_144566.3(ZNF700):c.1816A>G (p.Asn606Asp)	ZNF69, ZNF700 (N609D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197835	NM_144566.3(ZNF700):c.1676C>A (p.Thr559Asn)	ZNF69, ZNF700 (T559N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197834	NM_144566.3(ZNF700):c.151G>A (p.Glu51Lys)	ZNF69, ZNF700 (E51K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197833	NM_144566.3(ZNF700):c.1421A>G (p.Tyr474Cys)	ZNF69, ZNF700 (Y474C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197832	NM_144566.3(ZNF700):c.1123A>C (p.Lys375Gln)	ZNF69, ZNF700 (K378Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197753	NM_001364730.1(ZNF69):c.187G>T (p.Val63Leu)	ZNF69 (V49L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062391	GRCh37/hg19 19p13.2(chr19:10441330-13077352)x1	MIR199A1, ODAD3 +87 more	Copy number loss	not specified	GPathogenic
Select item 2649338	NM_144566.3(ZNF700):c.1182A>G (p.Gln394=)	ZNF69, ZNF700	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649337	NM_001364730.1(ZNF69):c.1005G>A (p.Thr335=)	ZNF69	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2599237	NM_144566.3(ZNF700):c.227A>G (p.Tyr76Cys)	ZNF69, ZNF700 (Y76C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594514	NM_001367172.2(ZNF763):c.479G>A (p.Arg160Lys)	ZNF69, ZNF763 (R160K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588958	NM_144566.3(ZNF700):c.497G>T (p.Cys166Phe)	ZNF69, ZNF700 (C169F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553744	NM_001367172.2(ZNF763):c.346A>C (p.Ile116Leu)	ZNF69, ZNF763 (I116L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550023	NM_001367172.2(ZNF763):c.749A>T (p.His250Leu)	ZNF69, ZNF763 (H128L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546137	NM_001367172.2(ZNF763):c.21G>T (p.Glu7Asp)	ZNF69, ZNF763 (E10D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546136	NM_001367172.2(ZNF763):c.17G>T (p.Cys6Phe)	ZNF69, ZNF763 (C9F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2544145	NM_001367172.2(ZNF763):c.166T>C (p.Tyr56His)	ZNF69, ZNF763 (Y58H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543953	NM_001364730.1(ZNF69):c.461A>G (p.Tyr154Cys)	ZNF69 (Y140C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525029	NM_144566.3(ZNF700):c.1926C>A (p.His642Gln)	ZNF69, ZNF700 (H645Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524741	NM_144566.3(ZNF700):c.1759A>G (p.Thr587Ala)	ZNF69, ZNF700 (T590A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521365	NM_144566.3(ZNF700):c.457G>A (p.Ala153Thr)	ZNF69, ZNF700 (A153T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511285	NM_144566.3(ZNF700):c.283A>G (p.Lys95Glu)	ZNF69, ZNF700 (K98E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494425	NM_001367172.2(ZNF763):c.31G>A (p.Val11Met)	ZNF69, ZNF763 (V13M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492982	NM_144566.3(ZNF700):c.911A>G (p.Lys304Arg)	ZNF69, ZNF700 (K304R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491531	NM_144566.3(ZNF700):c.856G>A (p.Ala286Thr)	ZNF69, ZNF700 (A286T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484799	NM_001367172.2(ZNF763):c.535A>G (p.Lys179Glu)	ZNF69, ZNF763 (K182E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483626	NM_001367172.2(ZNF763):c.821A>G (p.His274Arg)	ZNF69, ZNF763 (H152R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477318	NM_001364730.1(ZNF69):c.247T>G (p.Phe83Val)	ZNF69 (F69V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465625	NM_144566.3(ZNF700):c.1301G>A (p.Arg434Gln)	ZNF69, ZNF700 (R434Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464832	NM_001367172.2(ZNF763):c.384C>A (p.Asp128Glu)	ZNF69, ZNF763 (D128E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460209	NM_001364730.1(ZNF69):c.197G>A (p.Ser66Asn)	ZNF69 (S52N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2423817	NC_000019.9:g.(?_11277234)_(13249220_?)dup	ACP5, ANGPTL8 +68 more	Duplication	not provided	GUncertain significance
Select item 2422498	NC_000019.9:g.(?_10828919)_(13482613_?)dup	ACP5, ANGPTL8 +81 more	Duplication	Charcot-Marie-Tooth disease dominant intermediate B +4 more	GUncertain significance
Select item 2408467	NM_001367172.2(ZNF763):c.964C>T (p.Arg322Cys)	ZNF69, ZNF763 (R200C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404171	NM_144566.3(ZNF700):c.2048A>G (p.Asn683Ser)	ZNF69, ZNF700 (N686S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399881	NM_001367172.2(ZNF763):c.431A>C (p.Tyr144Ser)	ZNF69, ZNF763 (Y146S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398264	NM_001367172.2(ZNF763):c.919A>G (p.Thr307Ala)	ZNF69, ZNF763 (T309A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397331	NM_001364730.1(ZNF69):c.184T>A (p.Ser62Thr)	ZNF69 (S62T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381052	NM_144566.3(ZNF700):c.1960G>A (p.Glu654Lys)	ZNF69, ZNF700 (E657K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357462	NM_144566.3(ZNF700):c.589A>G (p.Lys197Glu)	ZNF69, ZNF700 (K197E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347760	NM_001367172.2(ZNF763):c.1130T>C (p.Leu377Ser)	ZNF69, ZNF763 (L379S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328692	NM_144566.3(ZNF700):c.1400C>G (p.Thr467Ser)	ZNF69, ZNF700 (T467S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326678	NM_144566.3(ZNF700):c.1828C>A (p.His610Asn)	ZNF69, ZNF700 (H610N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315896	NM_144566.3(ZNF700):c.1856C>G (p.Pro619Arg)	ZNF69, ZNF700 (P622R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310305	NM_001367172.2(ZNF763):c.494A>G (p.Asn165Ser)	ZNF69, ZNF763 (N165S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308985	NM_001367172.2(ZNF763):c.847C>T (p.Pro283Ser)	ZNF69, ZNF763 (P161S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300880	NM_144566.3(ZNF700):c.1217G>A (p.Arg406Gln)	ZNF69, ZNF700 (R409Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284640	NM_144566.3(ZNF700):c.64G>A (p.Asp22Asn)	ZNF69, ZNF700 (D22N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275481	NM_001367172.2(ZNF763):c.106A>G (p.Thr36Ala)	ZNF69, ZNF763 (T36A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275066	NM_144566.3(ZNF700):c.767G>T (p.Gly256Val)	ZNF69, ZNF700 (G256V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268319	NM_144566.3(ZNF700):c.513T>G (p.Asn171Lys)	ZNF69, ZNF700 (N174K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268309	NM_144566.3(ZNF700):c.710A>G (p.Tyr237Cys)	ZNF69, ZNF700 (Y240C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2268153	NM_001367172.2(ZNF763):c.112A>G (p.Arg38Gly)	ZNF69, ZNF763 (R38G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258785	NM_001367172.2(ZNF763):c.416A>C (p.Tyr139Ser)	ZNF69, ZNF763 (Y142S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250434	NM_144566.3(ZNF700):c.446C>T (p.Thr149Ile)	ZNF69, ZNF700 (T149I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2243442	NM_144566.3(ZNF700):c.1780T>C (p.Cys594Arg)	ZNF69, ZNF700 (C594R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236642	NM_144566.3(ZNF700):c.254G>C (p.Ser85Thr)	ZNF69, ZNF700 (S88T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234330	NM_001367172.2(ZNF763):c.569G>A (p.Arg190His)	ZNF69, ZNF763 (R192H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2228585	NM_144566.3(ZNF700):c.1606T>A (p.Tyr536Asn)	ZNF69, ZNF700 (Y539N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223325	NM_144566.3(ZNF700):c.286G>C (p.Glu96Gln)	ZNF69, ZNF700 (E96Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223209	NM_144566.3(ZNF700):c.4C>G (p.Pro2Ala)	ZNF69, ZNF700 (P2A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223098	NM_144566.3(ZNF700):c.1068C>G (p.Asn356Lys)	ZNF69, ZNF700 (N359K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218688	NM_144566.3(ZNF700):c.299G>T (p.Cys100Phe)	ZNF69, ZNF700 (C103F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217920	NM_001364730.1(ZNF69):c.226T>C (p.Tyr76His)	ZNF69 (Y76H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209578	NM_144566.3(ZNF700):c.1910T>C (p.Met637Thr)	ZNF69, ZNF700 (M640T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208379	NM_144566.3(ZNF700):c.1040T>C (p.Ile347Thr)	ZNF69, ZNF700 (I347T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2207494	NM_144566.3(ZNF700):c.1165C>T (p.Arg389Cys)	ZNF69, ZNF700 (R389C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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