"Ambry Genetics"[submitter] AND "ZNF69"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2397331	NM_001364730.1(ZNF69):c.184T>A (p.Ser62Thr)	ZNF69 (S62T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460209	NM_001364730.1(ZNF69):c.197G>A (p.Ser66Asn)	ZNF69 (S52N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217920	NM_001364730.1(ZNF69):c.226T>C (p.Tyr76His)	ZNF69 (Y76H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477318	NM_001364730.1(ZNF69):c.247T>G (p.Phe83Val)	ZNF69 (F69V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2543953	NM_001364730.1(ZNF69):c.461A>G (p.Tyr154Cys)	ZNF69 (Y140C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223209	NM_144566.3(ZNF700):c.4C>G (p.Pro2Ala)	ZNF69, ZNF700 (P2A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2284640	NM_144566.3(ZNF700):c.64G>A (p.Asp22Asn)	ZNF69, ZNF700 (D22N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599237	NM_144566.3(ZNF700):c.227A>G (p.Tyr76Cys)	ZNF69, ZNF700 (Y76C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236642	NM_144566.3(ZNF700):c.254G>C (p.Ser85Thr)	ZNF69, ZNF700 (S88T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511285	NM_144566.3(ZNF700):c.283A>G (p.Lys95Glu)	ZNF69, ZNF700 (K98E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223325	NM_144566.3(ZNF700):c.286G>C (p.Glu96Gln)	ZNF69, ZNF700 (E96Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218688	NM_144566.3(ZNF700):c.299G>T (p.Cys100Phe)	ZNF700, ZNF69 (C103F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250434	NM_144566.3(ZNF700):c.446C>T (p.Thr149Ile)	ZNF700, ZNF69 (T149I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2521365	NM_144566.3(ZNF700):c.457G>A (p.Ala153Thr)	ZNF69, ZNF700 (A153T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588958	NM_144566.3(ZNF700):c.497G>T (p.Cys166Phe)	ZNF69, ZNF700 (C169F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2268319	NM_144566.3(ZNF700):c.513T>G (p.Asn171Lys)	ZNF69, ZNF700 (N174K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357462	NM_144566.3(ZNF700):c.589A>G (p.Lys197Glu)	ZNF700, ZNF69 (K197E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2268309	NM_144566.3(ZNF700):c.710A>G (p.Tyr237Cys)	ZNF700, ZNF69 (Y240C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2275066	NM_144566.3(ZNF700):c.767G>T (p.Gly256Val)	ZNF69, ZNF700 (G256V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491531	NM_144566.3(ZNF700):c.856G>A (p.Ala286Thr)	ZNF69, ZNF700 (A286T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492982	NM_144566.3(ZNF700):c.911A>G (p.Lys304Arg)	ZNF69, ZNF700 (K304R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208379	NM_144566.3(ZNF700):c.1040T>C (p.Ile347Thr)	ZNF69, ZNF700 (I347T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2223098	NM_144566.3(ZNF700):c.1068C>G (p.Asn356Lys)	ZNF69, ZNF700 (N359K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207494	NM_144566.3(ZNF700):c.1165C>T (p.Arg389Cys)	ZNF69, ZNF700 (R389C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300880	NM_144566.3(ZNF700):c.1217G>A (p.Arg406Gln)	ZNF69, ZNF700 (R409Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465625	NM_144566.3(ZNF700):c.1301G>A (p.Arg434Gln)	ZNF69, ZNF700 (R434Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328692	NM_144566.3(ZNF700):c.1400C>G (p.Thr467Ser)	ZNF69, ZNF700 (T467S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2228585	NM_144566.3(ZNF700):c.1606T>A (p.Tyr536Asn)	ZNF69, ZNF700 (Y539N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524741	NM_144566.3(ZNF700):c.1759A>G (p.Thr587Ala)	ZNF69, ZNF700 (T590A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243442	NM_144566.3(ZNF700):c.1780T>C (p.Cys594Arg)	ZNF69, ZNF700 (C594R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326678	NM_144566.3(ZNF700):c.1828C>A (p.His610Asn)	ZNF69, ZNF700 (H610N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315896	NM_144566.3(ZNF700):c.1856C>G (p.Pro619Arg)	ZNF700, ZNF69 (P622R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209578	NM_144566.3(ZNF700):c.1910T>C (p.Met637Thr)	ZNF700, ZNF69 (M640T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525029	NM_144566.3(ZNF700):c.1926C>A (p.His642Gln)	ZNF69, ZNF700 (H645Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381052	NM_144566.3(ZNF700):c.1960G>A (p.Glu654Lys)	ZNF69, ZNF700 (E657K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404171	NM_144566.3(ZNF700):c.2048A>G (p.Asn683Ser)	ZNF69, ZNF700 (N686S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	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)	Inborn genetic diseases	GLikely benign
Select item 2546137	NM_001367172.2(ZNF763):c.21G>T (p.Glu7Asp)	ZNF69, ZNF763 (E10D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2268153	NM_001367172.2(ZNF763):c.112A>G (p.Arg38Gly)	ZNF69, ZNF763 (R38G +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2544145	NM_001367172.2(ZNF763):c.166T>C (p.Tyr56His)	ZNF69, ZNF763 (Y58H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2464832	NM_001367172.2(ZNF763):c.384C>A (p.Asp128Glu)	ZNF69, ZNF763 (D128E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2258785	NM_001367172.2(ZNF763):c.416A>C (p.Tyr139Ser)	ZNF763, ZNF69 (Y142S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399881	NM_001367172.2(ZNF763):c.431A>C (p.Tyr144Ser)	ZNF69, ZNF763 (Y146S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2594514	NM_001367172.2(ZNF763):c.479G>A (p.Arg160Lys)	ZNF69, ZNF763 (R160K +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2310305	NM_001367172.2(ZNF763):c.494A>G (p.Asn165Ser)	ZNF69, ZNF763 (N165S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484799	NM_001367172.2(ZNF763):c.535A>G (p.Lys179Glu)	ZNF69, ZNF763 (K182E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2234330	NM_001367172.2(ZNF763):c.569G>A (p.Arg190His)	ZNF69, ZNF763 (R192H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2550023	NM_001367172.2(ZNF763):c.749A>T (p.His250Leu)	ZNF69, ZNF763 (H128L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483626	NM_001367172.2(ZNF763):c.821A>G (p.His274Arg)	ZNF69, ZNF763 (H152R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2308985	NM_001367172.2(ZNF763):c.847C>T (p.Pro283Ser)	ZNF763, ZNF69 (P161S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398264	NM_001367172.2(ZNF763):c.919A>G (p.Thr307Ala)	ZNF763, ZNF69 (T309A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408467	NM_001367172.2(ZNF763):c.964C>T (p.Arg322Cys)	ZNF763, ZNF69 (R200C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347760	NM_001367172.2(ZNF763):c.1130T>C (p.Leu377Ser)	ZNF69, ZNF763 (L379S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	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: 56