"Ambry Genetics"[submitter] AND "ZNF600"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258861	NM_001321866.4(ZNF600):c.2368C>T (p.Leu790Phe)	ZNF600 (L721F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197100	NM_001321866.4(ZNF600):c.2336T>C (p.Ile779Thr)	ZNF600 (I710T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293844	NM_001321866.4(ZNF600):c.2326T>C (p.Ser776Pro)	ZNF600 (S707P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266864	NM_001321866.4(ZNF600):c.2251A>G (p.Lys751Glu)	ZNF600 (K751E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321140	NM_001321866.4(ZNF600):c.2249T>A (p.Leu750Gln)	ZNF600 (L681Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385548	NM_001321866.4(ZNF600):c.2215G>T (p.Val739Phe)	ZNF600 (V670F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337021	NM_001321866.4(ZNF600):c.2143G>C (p.Val715Leu)	ZNF600 (V715L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197099	NM_001321866.4(ZNF600):c.2131A>G (p.Thr711Ala)	ZNF600 (T711A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197098	NM_001321866.4(ZNF600):c.2104G>A (p.Ala702Thr)	ZNF600 (A633T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2481360	NM_001321866.4(ZNF600):c.2101C>T (p.His701Tyr)	ZNF600 (H632Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197097	NM_001321866.4(ZNF600):c.2087T>G (p.Leu696Arg)	ZNF600 (L696R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197096	NM_001321866.4(ZNF600):c.2079A>C (p.Gln693His)	ZNF600 (Q693H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283023	NM_001321866.4(ZNF600):c.2011A>G (p.Arg671Gly)	ZNF600 (R602G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258858	NM_001321866.4(ZNF600):c.1972A>G (p.Lys658Glu)	ZNF600 (K589E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197095	NM_001321866.4(ZNF600):c.1963G>A (p.Val655Ile)	ZNF600 (V655I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508872	NM_001321866.4(ZNF600):c.1961C>T (p.Thr654Met)	ZNF600 (T585M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384172	NM_001321866.4(ZNF600):c.1925G>A (p.Arg642His)	ZNF600 (R573H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529110	NM_001321866.4(ZNF600):c.1870A>G (p.Lys624Glu)	ZNF600 (K624E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555388	NM_001321866.4(ZNF600):c.1849C>A (p.His617Asn)	ZNF600 (H548N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382270	NM_001321866.4(ZNF600):c.1832A>G (p.His611Arg)	ZNF600 (H542R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403137	NM_001321866.4(ZNF600):c.1765C>T (p.His589Tyr)	ZNF600 (H589Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258857	NM_001321866.4(ZNF600):c.1736G>A (p.Arg579Lys)	ZNF600 (R579K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197094	NM_001321866.4(ZNF600):c.1735A>T (p.Arg579Trp)	ZNF600 (R510W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613354	NM_001321866.4(ZNF600):c.1714T>A (p.Cys572Ser)	ZNF600 (C572S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256407	NM_001321866.4(ZNF600):c.1621T>A (p.Cys541Ser)	ZNF600 (C472S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197093	NM_001321866.4(ZNF600):c.1597C>G (p.His533Asp)	ZNF600 (H464D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514487	NM_001321866.4(ZNF600):c.1538A>C (p.Tyr513Ser)	ZNF600 (Y444S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493994	NM_001321866.4(ZNF600):c.1455T>G (p.Cys485Trp)	ZNF600 (C485W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461579	NM_001321866.4(ZNF600):c.1346A>C (p.His449Pro)	ZNF600 (H380P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592121	NM_001321866.4(ZNF600):c.1334A>G (p.His445Arg)	ZNF600 (H376R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258859	NM_001321866.4(ZNF600):c.1321T>G (p.Ser441Ala)	ZNF600 (S372A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592120	NM_001321866.4(ZNF600):c.1312C>G (p.His438Asp)	ZNF600 (H438D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317426	NM_001321866.4(ZNF600):c.1295G>A (p.Cys432Tyr)	ZNF600 (C432Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306877	NM_001321866.4(ZNF600):c.1210T>G (p.Cys404Gly)	ZNF600 (C335G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258856	NM_001321866.4(ZNF600):c.1202G>A (p.Cys401Tyr)	ZNF600 (C401Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365791	NM_001321866.4(ZNF600):c.1156C>A (p.Leu386Ile)	ZNF600 (L386I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197104	NM_001321866.4(ZNF600):c.1145G>A (p.Arg382Gln)	ZNF600 (R313Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596807	NM_001321866.4(ZNF600):c.1084C>T (p.Arg362Cys)	ZNF600 (R362C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543648	NM_001321866.4(ZNF600):c.1081C>G (p.His361Asp)	ZNF600 (H292D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360063	NM_001321866.4(ZNF600):c.1078C>T (p.Arg360Cys)	ZNF600 (R291C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492112	NM_001321866.4(ZNF600):c.1028A>G (p.Tyr343Cys)	ZNF600 (Y343C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623013	NM_001321866.4(ZNF600):c.932C>T (p.Ala311Val)	ZNF600 (A242V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258855	NM_001321866.4(ZNF600):c.916C>T (p.Arg306Cys)	ZNF600 (R237C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402399	NM_001321866.4(ZNF600):c.867T>G (p.Cys289Trp)	ZNF600 (C289W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341033	NM_001321866.4(ZNF600):c.833G>A (p.Cys278Tyr)	ZNF600 (C278Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520918	NM_001321866.4(ZNF600):c.823A>G (p.Thr275Ala)	ZNF600 (T206A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2260840	NM_001321866.4(ZNF600):c.751A>G (p.Ile251Val)	ZNF600 (I251V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197103	NM_001321866.4(ZNF600):c.707G>A (p.Ser236Asn)	ZNF600 (S236N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459410	NM_001321866.4(ZNF600):c.677T>C (p.Met226Thr)	ZNF600 (M226T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197102	NM_001321866.4(ZNF600):c.664C>G (p.Gln222Glu)	ZNF600 (Q153E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300192	NM_001321866.4(ZNF600):c.638C>T (p.Pro213Leu)	ZNF600 (P213L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2300191	NM_001321866.4(ZNF600):c.634T>C (p.Ser212Pro)	ZNF600 (S212P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533692	NM_001321866.4(ZNF600):c.623A>G (p.Tyr208Cys)	ZNF600 (Y208C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231393	NM_001321866.4(ZNF600):c.599C>T (p.Pro200Leu)	ZNF600 (P131L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553475	NM_001321866.4(ZNF600):c.597G>T (p.Arg199Ser)	ZNF600 (R199S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197101	NM_001321866.4(ZNF600):c.523A>G (p.Lys175Glu)	ZNF600 (K175E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550051	NM_001321866.4(ZNF600):c.520G>C (p.Gly174Arg)	ZNF600 (G105R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375808	NM_001321866.4(ZNF600):c.425A>G (p.His142Arg)	ZNF600 (H142R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231132	NM_001321866.4(ZNF600):c.386T>C (p.Met129Thr)	ZNF600 (M129T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469629	NM_001321866.4(ZNF600):c.298G>A (p.Asp100Asn)	ZNF600 (D100N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276225	NM_001321866.4(ZNF600):c.293T>C (p.Ile98Thr)	ZNF600 (I29T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206375	NM_001321866.4(ZNF600):c.286T>C (p.Tyr96His)	ZNF600 (Y27H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2206374	NM_001321866.4(ZNF600):c.280C>G (p.Gln94Glu)	ZNF600 (Q25E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2206372	NM_001321866.4(ZNF600):c.277T>C (p.Tyr93His)	ZNF600 (Y24H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2286566	NM_006969.5(ZNF28):c.2110T>C (p.Ser704Pro)	ZNF28, ZNF600 (S701P +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2308623	NM_006969.5(ZNF28):c.2000A>G (p.Glu667Gly)	ZNF28, ZNF600 (E614G +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2371008	NM_006969.5(ZNF28):c.1973G>T (p.Ser658Ile)	ZNF28, ZNF600 (S644I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2455887	NM_006969.5(ZNF28):c.1951G>A (p.Val651Ile)	ZNF28, ZNF600 (V648I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2238954	NM_006969.5(ZNF28):c.1930T>G (p.Phe644Val)	ZNF28, ZNF600 (F591V +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2623415	NM_006969.5(ZNF28):c.1883T>G (p.Leu628Arg)	ZNF28, ZNF600 (L614R +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2466093	NM_006969.5(ZNF28):c.1877G>A (p.Arg626His)	ZNF28, ZNF600 (R623H +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194842	NM_006969.5(ZNF28):c.1876C>T (p.Arg626Cys)	ZNF28, ZNF600 (R573C +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2204974	NM_006969.5(ZNF28):c.1844C>T (p.Thr615Ile)	ZNF28, ZNF600 (T562I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2561136	NM_006969.5(ZNF28):c.1829A>T (p.Asn610Ile)	ZNF28, ZNF600 (N574I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335349	NM_006969.5(ZNF28):c.1807G>A (p.Gly603Arg)	ZNF28, ZNF600 (G567R +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2589143	NM_006969.5(ZNF28):c.1789C>T (p.His597Tyr)	ZNF28, ZNF600 (H544Y +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2598223	NM_006969.5(ZNF28):c.1765C>T (p.Arg589Trp)	ZNF28, ZNF600 (R586W +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335340	NM_006969.5(ZNF28):c.1649C>T (p.Pro550Leu)	ZNF28, ZNF600 (P550L +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335345	NM_006969.5(ZNF28):c.1642G>A (p.Glu548Lys)	ZNF28, ZNF600 (E512K +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194841	NM_006969.5(ZNF28):c.1514G>A (p.Arg505Gln)	ZNF28, ZNF600 (R469Q +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2390698	NM_006969.5(ZNF28):c.1484A>G (p.Tyr495Cys)	ZNF28, ZNF600 (Y442C +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335342	NM_006969.5(ZNF28):c.1477A>C (p.Lys493Gln)	ZNF28, ZNF600 (K479Q +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194839	NM_006969.5(ZNF28):c.1451G>T (p.Arg484Ile)	ZNF28, ZNF600 (R448I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194838	NM_006969.5(ZNF28):c.1395A>T (p.Lys465Asn)	ZNF28, ZNF600 (K465N +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194837	NM_006969.5(ZNF28):c.1293A>G (p.Ile431Met)	ZNF28, ZNF600 (I417M +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2242852	NM_006969.5(ZNF28):c.1289G>A (p.Ser430Asn)	ZNF28, ZNF600 (S394N +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335344	NM_006969.5(ZNF28):c.1274A>C (p.Tyr425Ser)	ZNF28, ZNF600 (Y422S +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2288959	NM_006969.5(ZNF28):c.1250A>C (p.Asp417Ala)	ZNF28, ZNF600 (D381A +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2369836	NM_006969.5(ZNF28):c.1123A>G (p.Arg375Gly)	ZNF28, ZNF600 (R339G +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2468311	NM_006969.5(ZNF28):c.1120C>T (p.Arg374Cys)	ZNF28, ZNF600 (R321C +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2217170	NM_006969.5(ZNF28):c.1115G>A (p.Arg372His)	ZNF28, ZNF600 (R358H +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2296148	NM_006969.5(ZNF28):c.1074T>A (p.Asn358Lys)	ZNF28, ZNF600 (N344K +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2302208	NM_006969.5(ZNF28):c.1013G>A (p.Cys338Tyr)	ZNF28, ZNF600 (C335Y +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2410536	NM_006969.5(ZNF28):c.947C>T (p.Thr316Ile)	ZNF28, ZNF600 (T313I +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3335347	NM_006969.5(ZNF28):c.929G>T (p.Arg310Leu)	ZNF28, ZNF600 (R274L +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2519486	NM_006969.5(ZNF28):c.928C>T (p.Arg310Cys)	ZNF28, ZNF600 (R296C +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2605823	NM_006969.5(ZNF28):c.833A>G (p.Lys278Arg)	ZNF28, ZNF600 (K225R +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2553392	NM_006969.5(ZNF28):c.827G>T (p.Cys276Phe)	ZNF28, ZNF600 (C240F +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194848	NM_006969.5(ZNF28):c.797T>C (p.Ile266Thr)	ZNF28, ZNF600 (I266T +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 2220035	NM_006969.5(ZNF28):c.767G>A (p.Arg256Gln)	ZNF28, ZNF600 (R203Q +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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