ClinVar for Gene (Select 79776) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3236585	NM_024721.5(ZFHX4):c.7492T>C (p.Cys2498Arg)	ZFHX4 (C2472R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3234392	NM_024721.5(ZFHX4):c.9906A>C (p.Thr3302=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3234335	NM_024721.5(ZFHX4):c.9912C>A (p.Pro3304=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3193078	NM_024721.5(ZFHX4):c.9989T>C (p.Leu3330Pro)	ZFHX4 (L3330P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193077	NM_024721.5(ZFHX4):c.986A>G (p.Lys329Arg)	ZFHX4 (K329R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193076	NM_024721.5(ZFHX4):c.9644A>C (p.His3215Pro)	ZFHX4 (H3215P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193074	NM_024721.5(ZFHX4):c.9485C>T (p.Pro3162Leu)	ZFHX4 (P3136L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193073	NM_024721.5(ZFHX4):c.9295C>G (p.Pro3099Ala)	ZFHX4 (P3099A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193072	NM_024721.5(ZFHX4):c.9175A>G (p.Met3059Val)	ZFHX4 (M3059V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193071	NM_024721.5(ZFHX4):c.9031C>T (p.Leu3011Phe)	ZFHX4 (L3011F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193070	NM_024721.5(ZFHX4):c.8777G>A (p.Arg2926Gln)	ZFHX4 (R2900Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193069	NM_024721.5(ZFHX4):c.8693G>A (p.Arg2898His)	ZFHX4 (R2898H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193067	NM_024721.5(ZFHX4):c.8491G>A (p.Gly2831Arg)	ZFHX4 (G2805R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193066	NM_024721.5(ZFHX4):c.8423C>T (p.Thr2808Met)	ZFHX4 (T2808M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193064	NM_024721.5(ZFHX4):c.8150C>T (p.Thr2717Ile)	ZFHX4 (T2717I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193063	NM_024721.5(ZFHX4):c.7727C>T (p.Ala2576Val)	ZFHX4 (A2550V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193062	NM_024721.5(ZFHX4):c.7679C>T (p.Pro2560Leu)	ZFHX4 (P2560L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193061	NM_024721.5(ZFHX4):c.7577C>T (p.Ser2526Phe)	ZFHX4 (S2500F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193060	NM_024721.5(ZFHX4):c.6977A>G (p.Asp2326Gly)	ZFHX4 (D2326G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193059	NM_024721.5(ZFHX4):c.64T>C (p.Cys22Arg)	ZFHX4 (C22R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193058	NM_024721.5(ZFHX4):c.6253C>T (p.Pro2085Ser)	ZFHX4 (P2059S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193057	NM_024721.5(ZFHX4):c.6167C>T (p.Pro2056Leu)	ZFHX4 (P2056L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193056	NM_024721.5(ZFHX4):c.6140C>T (p.Pro2047Leu)	ZFHX4 (P2047L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193055	NM_024721.5(ZFHX4):c.5989C>G (p.Pro1997Ala)	ZFHX4 (P1971A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193054	NM_024721.5(ZFHX4):c.5831A>G (p.Asp1944Gly)	ZFHX4 (D1918G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193053	NM_024721.5(ZFHX4):c.5804G>A (p.Gly1935Asp)	ZFHX4 (G1935D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193052	NM_024721.5(ZFHX4):c.5716G>A (p.Gly1906Arg)	ZFHX4 (G1880R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193051	NM_024721.5(ZFHX4):c.568C>G (p.Gln190Glu)	ZFHX4 (Q190E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193050	NM_024721.5(ZFHX4):c.5651A>G (p.Asp1884Gly)	ZFHX4 (D1884G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193049	NM_024721.5(ZFHX4):c.5563T>C (p.Tyr1855His)	ZFHX4 (Y1855H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193047	NM_024721.5(ZFHX4):c.5101G>A (p.Glu1701Lys)	ZFHX4 (E1701K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193045	NM_024721.5(ZFHX4):c.5048C>T (p.Pro1683Leu)	ZFHX4 (P1683L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193044	NM_024721.5(ZFHX4):c.478C>T (p.Leu160Phe)	ZFHX4 (L160F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193043	NM_024721.5(ZFHX4):c.4049C>T (p.Pro1350Leu)	ZFHX4 (P1350L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193042	NM_024721.5(ZFHX4):c.4024G>A (p.Glu1342Lys)	ZFHX4 (E1316K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193041	NM_024721.5(ZFHX4):c.3976A>G (p.Met1326Val)	ZFHX4 (M1300V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3193040	NM_024721.5(ZFHX4):c.3760G>A (p.Val1254Ile)	ZFHX4 (V1228I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193039	NM_024721.5(ZFHX4):c.3737T>C (p.Ile1246Thr)	ZFHX4 (I1220T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193038	NM_024721.5(ZFHX4):c.3622G>A (p.Asp1208Asn)	ZFHX4 (D1208N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193037	NM_024721.5(ZFHX4):c.3200G>A (p.Arg1067His)	ZFHX4 (R1041H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193036	NM_024721.5(ZFHX4):c.2855C>G (p.Thr952Ser)	ZFHX4 (T926S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193035	NM_024721.5(ZFHX4):c.2671G>C (p.Glu891Gln)	ZFHX4 (E891Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193033	NM_024721.5(ZFHX4):c.241C>A (p.Pro81Thr)	ZFHX4 (P81T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193032	NM_024721.5(ZFHX4):c.2408A>G (p.Lys803Arg)	ZFHX4 (K803R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193031	NM_024721.5(ZFHX4):c.2266C>T (p.Pro756Ser)	ZFHX4 (P756S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193030	NM_024721.5(ZFHX4):c.2039G>A (p.Gly680Glu)	ZFHX4 (G680E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193029	NM_024721.5(ZFHX4):c.1603A>G (p.Lys535Glu)	ZFHX4 (K535E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193028	NM_024721.5(ZFHX4):c.1459G>C (p.Val487Leu)	ZFHX4 (V487L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193027	NM_024721.5(ZFHX4):c.1129G>A (p.Ala377Thr)	ZFHX4 (A377T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193025	NM_024721.5(ZFHX4):c.10544A>G (p.Tyr3515Cys)	ZFHX4 (Y3515C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193024	NM_024721.5(ZFHX4):c.10351G>T (p.Ala3451Ser)	ZFHX4 (A3425S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193023	NM_024721.5(ZFHX4):c.10252G>A (p.Ala3418Thr)	ZFHX4 (A3392T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3067694	NM_024721.5(ZFHX4):c.7517_7524dup (p.Gln2509fs)	ZFHX4 (Q2483fs +1 more)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 3063049	GRCh37/hg19 8q21.11(chr8:77361439-77694902)x3	ZFHX4	Copy number gain	not specified	GUncertain significance
Select item 3063025	GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	ADAM18, ADAM2 +240 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3060954	NM_024721.5(ZFHX4):c.6708C>T (p.Tyr2236=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3058764	NM_024721.5(ZFHX4):c.159G>C (p.Thr53=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3058442	NM_024721.5(ZFHX4):c.3174C>T (p.Val1058=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3058384	NM_024721.5(ZFHX4):c.10200G>A (p.Lys3400=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3057594	NM_024721.5(ZFHX4):c.447G>A (p.Gly149=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3057284	NM_024721.5(ZFHX4):c.10182C>T (p.Tyr3394=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3056977	NM_024721.5(ZFHX4):c.8772T>C (p.Asn2924=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3056770	NM_024721.5(ZFHX4):c.6793C>T (p.Leu2265=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3056218	NM_024721.5(ZFHX4):c.9355C>A (p.Pro3119Thr)	ZFHX4 (P3093T +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3053820	NM_024721.5(ZFHX4):c.4700A>G (p.His1567Arg)	ZFHX4 (H1541R +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3053805	NM_024721.5(ZFHX4):c.6147T>A (p.Pro2049=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3053194	NM_024721.5(ZFHX4):c.234G>A (p.Lys78=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3052499	NM_024721.5(ZFHX4):c.7749C>T (p.Asp2583=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3051212	NM_024721.5(ZFHX4):c.9783G>A (p.Gln3261=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3050099	NM_024721.5(ZFHX4):c.9133C>A (p.Arg3045=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3050059	NM_024721.5(ZFHX4):c.1475C>T (p.Thr492Ile)	ZFHX4 (T492I)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3050045	NM_024721.5(ZFHX4):c.1413T>C (p.Asp471=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3049996	NM_024721.5(ZFHX4):c.1119C>T (p.Asp373=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3048203	NM_024721.5(ZFHX4):c.9636C>T (p.Pro3212=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3045955	NM_024721.5(ZFHX4):c.9400G>A (p.Gly3134Ser)	ZFHX4 (G3108S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign
Select item 3045184	NM_024721.5(ZFHX4):c.10623C>G (p.Pro3541=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3044841	NM_024721.5(ZFHX4):c.6089C>T (p.Thr2030Met)	ZFHX4 (T2004M +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3043988	NM_024721.5(ZFHX4):c.609A>G (p.Lys203=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3043520	NM_024721.5(ZFHX4):c.4945A>T (p.Met1649Leu)	ZFHX4 (M1623L +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign
Select item 3043459	NM_024721.5(ZFHX4):c.3964+6C>A	ZFHX4	Single nucleotide variant (intron variant)	ZFHX4-related disorder	GLikely benign
Select item 3043055	NM_024721.5(ZFHX4):c.4419C>T (p.Ser1473=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3042716	NM_024721.5(ZFHX4):c.7581G>A (p.Pro2527=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3042101	NM_024721.5(ZFHX4):c.10461T>C (p.Val3487=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3042013	NM_024721.5(ZFHX4):c.4393G>A (p.Val1465Met)	ZFHX4 (V1439M +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign
Select item 3041672	NM_024721.5(ZFHX4):c.10162G>T (p.Ala3388Ser)	ZFHX4 (A3362S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign
Select item 3041492	NM_024721.5(ZFHX4):c.4471T>C (p.Tyr1491His)	ZFHX4 (Y1465H +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign
Select item 3041201	NM_024721.5(ZFHX4):c.1032T>C (p.Val344=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3040704	NM_024721.5(ZFHX4):c.6103C>T (p.Leu2035=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3040344	NM_024721.5(ZFHX4):c.3069C>T (p.His1023=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3039261	NM_024721.5(ZFHX4):c.5582T>G (p.Ile1861Ser)	ZFHX4 (I1835S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3038793	NM_024721.5(ZFHX4):c.3550G>C (p.Ala1184Pro)	ZFHX4 (A1158P +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3038664	NM_024721.5(ZFHX4):c.5820C>T (p.Gly1940=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3038466	NM_024721.5(ZFHX4):c.6141A>C (p.Pro2047=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3038346	NM_024721.5(ZFHX4):c.7179A>G (p.Pro2393=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GBenign
Select item 3037425	NM_024721.5(ZFHX4):c.196G>C (p.Val66Leu)	ZFHX4 (V66L)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3037269	NM_024721.5(ZFHX4):c.3817C>T (p.Pro1273Ser)	ZFHX4 (P1247S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GBenign
Select item 3035213	NM_024721.5(ZFHX4):c.3075G>A (p.Ala1025=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3034731	NM_024721.5(ZFHX4):c.5682C>A (p.Ser1894=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related disorder	GLikely benign
Select item 3031806	NM_024721.5(ZFHX4):c.6964C>T (p.Pro2322Ser)	ZFHX4 (P2296S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related disorder	GLikely benign

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