Related gene-specific medical variations for Gene (Select 90592) - ClinVar

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Items: 72

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3477977	NM_144566.3(ZNF700):c.1711A>C (p.Lys571Gln)	ZNF69, ZNF700 (K571Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477976	NM_144566.3(ZNF700):c.785C>T (p.Ser262Phe)	ZNF69, ZNF700 (S265F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477975	NM_144566.3(ZNF700):c.1652T>C (p.Leu551Pro)	ZNF69, ZNF700 (L551P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477974	NM_144566.3(ZNF700):c.1476T>A (p.His492Gln)	ZNF69, ZNF700 (H492Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477973	NM_144566.3(ZNF700):c.259A>G (p.Ile87Val)	ZNF69, ZNF700 (I90V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477972	NM_144566.3(ZNF700):c.2132A>G (p.Lys711Arg)	ZNF69, ZNF700 (K714R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477971	NM_144566.3(ZNF700):c.629G>A (p.Arg210Gln)	ZNF69, ZNF700 (R210Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477970	NM_144566.3(ZNF700):c.986C>G (p.Ser329Cys)	ZNF69, ZNF700 (S332C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477968	NM_144566.3(ZNF700):c.1672C>T (p.His558Tyr)	ZNF69, ZNF700 (H561Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477967	NM_144566.3(ZNF700):c.2128G>A (p.Gly710Arg)	ZNF69, ZNF700 (G713R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477966	NM_144566.3(ZNF700):c.2003G>A (p.Arg668Lys)	ZNF69, ZNF700 (R671K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477965	NM_144566.3(ZNF700):c.275A>G (p.Asn92Ser)	ZNF69, ZNF700 (N92S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477964	NM_144566.3(ZNF700):c.494A>G (p.Lys165Arg)	ZNF69, ZNF700 (K165R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3477963	NM_144566.3(ZNF700):c.1475A>G (p.His492Arg)	ZNF69, ZNF700 (H492R +1 more)	Single nucleotide variant (missense variant)	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 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 2649338	NM_144566.3(ZNF700):c.1182A>G (p.Gln394=)	ZNF69, ZNF700	Single nucleotide variant (synonymous variant)	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 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 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 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 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 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 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 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 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 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 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 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 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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Items: 72