ClinVar for Gene (Select 23036) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3373635	NM_015021.3(ZNF292):c.3831A>G (p.Ser1277=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3372593	NM_015021.3(ZNF292):c.7044T>G (p.Ile2348Met)	ZNF292 (I2208M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3372473	NM_015021.3(ZNF292):c.168+4A>T	LOC129996783, ZNF292	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3372451	NM_015021.3(ZNF292):c.7378G>C (p.Asp2460His)	ZNF292 (D2320H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3372097	NM_015021.3(ZNF292):c.4505C>G (p.Thr1502Arg)	ZNF292 (T1362R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369554	NM_015021.3(ZNF292):c.2743G>A (p.Gly915Arg)	ZNF292 (G775R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369387	NM_015021.3(ZNF292):c.5820T>G (p.Asn1940Lys)	ZNF292 (N1800K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368821	NM_015021.3(ZNF292):c.1232A>G (p.Asn411Ser)	ZNF292 (N271S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368820	NM_015021.3(ZNF292):c.5080A>C (p.Asn1694His)	ZNF292 (N1554H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368392	NM_015021.3(ZNF292):c.1094C>G (p.Thr365Ser)	ZNF292 (T225S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367553	NM_015021.3(ZNF292):c.6305T>A (p.Leu2102His)	ZNF292 (L1962H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367534	NM_015021.3(ZNF292):c.1957G>T (p.Gly653Cys)	ZNF292 (G513C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367092	NM_015021.3(ZNF292):c.5920T>C (p.Phe1974Leu)	ZNF292 (F1834L +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3365503	NM_015021.3(ZNF292):c.5440T>G (p.Ser1814Ala)	ZNF292 (S1674A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365484	NM_015021.3(ZNF292):c.5298G>C (p.Met1766Ile)	ZNF292 (M1626I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365065	NM_015021.3(ZNF292):c.7531A>G (p.Ser2511Gly)	ZNF292 (S2371G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364961	NM_015021.3(ZNF292):c.5578T>C (p.Cys1860Arg)	ZNF292 (C1720R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364643	NM_015021.3(ZNF292):c.2036A>G (p.Asn679Ser)	ZNF292 (N539S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364241	NM_015021.3(ZNF292):c.2462A>C (p.Gln821Pro)	ZNF292 (Q681P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363384	NM_015021.3(ZNF292):c.5775A>C (p.Lys1925Asn)	ZNF292 (K1785N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3362458	NM_015021.3(ZNF292):c.995T>C (p.Phe332Ser)	ZNF292 (F192S +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3361621	NM_015021.3(ZNF292):c.5285T>C (p.Ile1762Thr)	ZNF292 (I1622T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361489	NM_015021.3(ZNF292):c.4746T>A (p.Asn1582Lys)	ZNF292 (N1442K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360753	NM_015021.3(ZNF292):c.4493G>T (p.Gly1498Val)	ZNF292 (G1358V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359453	NM_015021.3(ZNF292):c.554C>T (p.Ala185Val)	ZNF292 (A185V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3351489	NM_015021.3(ZNF292):c.1226T>C (p.Leu409Ser)	ZNF292 (L269S +1 more)	Single nucleotide variant (missense variant)	ZNF292-related disorder	GUncertain significance
Select item 3351241	NM_015021.3(ZNF292):c.6431C>A (p.Pro2144His)	ZNF292 (P2004H +1 more)	Single nucleotide variant (missense variant)	ZNF292-related disorder	GLikely benign
Select item 3349097	NM_015021.3(ZNF292):c.4505C>T (p.Thr1502Ile)	ZNF292 (T1362I +1 more)	Single nucleotide variant (missense variant)	ZNF292-related disorder	GUncertain significance
Select item 3343936	NM_015021.3(ZNF292):c.6517C>T (p.Arg2173Ter)	ZNF292 (R2033* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3342055	NM_015021.3(ZNF292):c.2904A>G (p.Thr968=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3341731	NM_015021.3(ZNF292):c.7659A>T (p.Ala2553=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3335406	NM_015021.3(ZNF292):c.4027G>A (p.Val1343Ile)	ZNF292 (V1203I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335405	NM_015021.3(ZNF292):c.4720G>T (p.Asp1574Tyr)	ZNF292 (D1574Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335404	NM_015021.3(ZNF292):c.7496G>A (p.Ser2499Asn)	ZNF292 (S2359N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335402	NM_015021.3(ZNF292):c.3578C>T (p.Pro1193Leu)	ZNF292 (P1193L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335401	NM_015021.3(ZNF292):c.3041G>T (p.Gly1014Val)	ZNF292 (G874V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335400	NM_015021.3(ZNF292):c.2911C>T (p.His971Tyr)	ZNF292 (H831Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335399	NM_015021.3(ZNF292):c.324A>G (p.Leu108=)	ZNF292	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3335398	NM_015021.3(ZNF292):c.6758A>G (p.Asp2253Gly)	ZNF292 (D2113G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335397	NM_015021.3(ZNF292):c.845G>A (p.Arg282His)	ZNF292 (R282H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335396	NM_015021.3(ZNF292):c.4585C>A (p.Pro1529Thr)	ZNF292 (P1389T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335395	NM_015021.3(ZNF292):c.5347A>G (p.Thr1783Ala)	ZNF292 (T1643A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335394	NM_015021.3(ZNF292):c.5131G>C (p.Glu1711Gln)	ZNF292 (E1711Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335393	NM_015021.3(ZNF292):c.3227C>T (p.Pro1076Leu)	ZNF292 (P1076L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335392	NM_015021.3(ZNF292):c.7503G>C (p.Glu2501Asp)	ZNF292 (E2501D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3335391	NM_015021.3(ZNF292):c.3061T>G (p.Leu1021Val)	ZNF292 (L1021V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3335390	NM_015021.3(ZNF292):c.1562T>G (p.Ile521Arg)	ZNF292 (I381R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3257330	NM_015021.3(ZNF292):c.7614T>G (p.Asn2538Lys)	ZNF292 (N2398K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3257251	NM_015021.3(ZNF292):c.1446G>C (p.Val482=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3257165	NM_015021.3(ZNF292):c.168+13941G>T	ZNF292	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3257144	NM_015021.3(ZNF292):c.3820C>G (p.Leu1274Val)	ZNF292 (L1134V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3257129	NM_015021.3(ZNF292):c.5648T>C (p.Ile1883Thr)	ZNF292 (I1743T +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3256981	NM_015021.3(ZNF292):c.7185A>G (p.Ser2395=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3255095	NM_015021.3(ZNF292):c.1717del (p.Ile573fs)	ZNF292 (I433fs +1 more)	Deletion (frameshift variant)	Intellectual developmental disorder, autosomal dominant 64	GPathogenic
Select item 3242240	NM_015021.3(ZNF292):c.4196_4197insAA (p.Tyr1399Ter)	ZNF292 (Y1259* +1 more)	Insertion (nonsense)	Autosomal dominant non-syndromic intellectual disability	GLikely pathogenic
Select item 3241993	NM_015021.3(ZNF292):c.5640C>G (p.Ile1880Met)	ZNF292 (I1740M +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3239332	NM_015021.3(ZNF292):c.5563A>G (p.Thr1855Ala)	ZNF292 (T1715A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3239098	NM_015021.3(ZNF292):c.48C>A (p.Gly16=)	LOC129996783, ZNF292	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3236241	NM_015021.3(ZNF292):c.741+5G>A	ZNF292	Single nucleotide variant (intron variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3234939	NM_015021.3(ZNF292):c.4825A>G (p.Ile1609Val)	ZNF292 (I1469V +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3233950	NM_015021.3(ZNF292):c.4726C>A (p.Leu1576Ile)	ZNF292 (L1436I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194991	NM_015021.3(ZNF292):c.797A>G (p.Glu266Gly)	ZNF292 (E266G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194990	NM_015021.3(ZNF292):c.7934G>C (p.Cys2645Ser)	ZNF292 (C2645S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194989	NM_015021.3(ZNF292):c.7685G>A (p.Arg2562His)	ZNF292 (R2422H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194988	NM_015021.3(ZNF292):c.7498G>T (p.Val2500Leu)	ZNF292 (V2360L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194986	NM_015021.3(ZNF292):c.7358C>T (p.Thr2453Met)	ZNF292 (T2313M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194984	NM_015021.3(ZNF292):c.5950_5956del (p.Ile1984fs)	ZNF292 (I1844fs +1 more)	Deletion (frameshift variant)	Inborn genetic diseases	GPathogenic
Select item 3194982	NM_015021.3(ZNF292):c.5770G>C (p.Gly1924Arg)	ZNF292 (G1784R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194981	NM_015021.3(ZNF292):c.5676T>G (p.Ile1892Met)	ZNF292 (I1892M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194980	NM_015021.3(ZNF292):c.5654C>A (p.Pro1885Gln)	ZNF292 (P1745Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194979	NM_015021.3(ZNF292):c.5600T>C (p.Val1867Ala)	ZNF292 (V1727A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194978	NM_015021.3(ZNF292):c.5446A>G (p.Ile1816Val)	ZNF292 (I1676V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194977	NM_015021.3(ZNF292):c.5389T>A (p.Ser1797Thr)	ZNF292 (S1657T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194976	NM_015021.3(ZNF292):c.5202T>A (p.Asn1734Lys)	ZNF292 (N1594K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194975	NM_015021.3(ZNF292):c.4757C>G (p.Ser1586Cys)	ZNF292 (S1446C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194974	NM_015021.3(ZNF292):c.4738G>A (p.Val1580Ile)	ZNF292 (V1440I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194973	NM_015021.3(ZNF292):c.4693A>G (p.Ser1565Gly)	ZNF292 (S1565G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194972	NM_015021.3(ZNF292):c.4687G>A (p.Glu1563Lys)	ZNF292 (E1563K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194971	NM_015021.3(ZNF292):c.4003G>A (p.Ala1335Thr)	ZNF292 (A1195T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194970	NM_015021.3(ZNF292):c.3622G>A (p.Glu1208Lys)	ZNF292 (E1208K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194968	NM_015021.3(ZNF292):c.3257C>T (p.Thr1086Ile)	ZNF292 (T946I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194967	NM_015021.3(ZNF292):c.3209G>A (p.Ser1070Asn)	ZNF292 (S1070N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194966	NM_015021.3(ZNF292):c.3196A>G (p.Lys1066Glu)	ZNF292 (K1066E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194965	NM_015021.3(ZNF292):c.2782C>A (p.Pro928Thr)	ZNF292 (P928T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194964	NM_015021.3(ZNF292):c.2593A>T (p.Ile865Phe)	ZNF292 (I865F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194962	NM_015021.3(ZNF292):c.2083T>C (p.Phe695Leu)	ZNF292 (F555L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194961	NM_015021.3(ZNF292):c.2023C>T (p.Pro675Ser)	ZNF292 (P675S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3194960	NM_015021.3(ZNF292):c.1511A>G (p.Asn504Ser)	ZNF292 (N364S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3194959	NM_015021.3(ZNF292):c.1139C>T (p.Pro380Leu)	ZNF292 (P240L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3068522	NM_015021.3(ZNF292):c.5233C>T (p.Gln1745Ter)	ZNF292 (Q1605* +1 more)	Single nucleotide variant (nonsense)	Intellectual developmental disorder, autosomal dominant 64	GPathogenic
Select item 3067823	NM_015021.3(ZNF292):c.6239G>T (p.Arg2080Leu)	ZNF292 (R1940L +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3067654	NM_015021.3(ZNF292):c.4917T>C (p.Ile1639=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3067543	NM_015021.3(ZNF292):c.7797T>C (p.Leu2599=)	ZNF292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3067312	NM_015021.3(ZNF292):c.5422G>A (p.Asp1808Asn)	ZNF292 (D1668N +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3065419	NM_015021.3(ZNF292):c.5845T>C (p.Cys1949Arg)	ZNF292 (C1809R +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3064908	NM_015021.3(ZNF292):c.4153A>T (p.Thr1385Ser)	ZNF292 (T1245S +1 more)	Single nucleotide variant (missense variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 3061707	NM_015021.3(ZNF292):c.3441A>G (p.Thr1147=)	ZNF292	Single nucleotide variant (synonymous variant)	ZNF292-related disorder	GLikely benign
Select item 3061135	NM_015021.3(ZNF292):c.407C>T (p.Ala136Val)	ZNF292 (A136V)	Single nucleotide variant (5 prime UTR variant +1 more)	ZNF292-related disorder	GUncertain significance
Select item 3060625	NM_015021.3(ZNF292):c.5994G>A (p.Pro1998=)	ZNF292	Single nucleotide variant (synonymous variant)	ZNF292-related disorder	GBenign
Select item 3060017	NM_015021.3(ZNF292):c.6453A>G (p.Glu2151=)	ZNF292	Single nucleotide variant (synonymous variant)	ZNF292-related disorder	GLikely benign

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