ClinVar for Gene (Select 463) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3236590	NM_006885.4(ZFHX3):c.76G>T (p.Glu26Ter)	ZFHX3 (E26*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 3234463	NM_006885.4(ZFHX3):c.9582A>G (p.Gln3194=)	ZFHX3-AS1, ZFHX3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3233763	NM_006885.4(ZFHX3):c.2815G>A (p.Asp939Asn)	ZFHX3 (D25N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193021	NM_006885.4(ZFHX3):c.9590A>C (p.Gln3197Pro)	ZFHX3, ZFHX3-AS1 (Q2283P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193020	NM_006885.4(ZFHX3):c.9350C>T (p.Ala3117Val)	ZFHX3, ZFHX3-AS1 (A3117V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193019	NM_006885.4(ZFHX3):c.923C>T (p.Thr308Ile)	ZFHX3 (T308I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193017	NM_006885.4(ZFHX3):c.8645C>T (p.Ala2882Val)	ZFHX3, ZFHX3-AS1 (A1968V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193016	NM_006885.4(ZFHX3):c.8474T>G (p.Phe2825Cys)	ZFHX3, ZFHX3-AS1 (F2825C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193015	NM_006885.4(ZFHX3):c.8372C>G (p.Thr2791Ser)	ZFHX3, ZFHX3-AS1 (T1877S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193014	NM_006885.4(ZFHX3):c.8248A>G (p.Met2750Val)	ZFHX3, ZFHX3-AS1 (M1836V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193012	NM_006885.4(ZFHX3):c.7915C>G (p.Gln2639Glu)	ZFHX3-AS1, ZFHX3 (Q1725E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193011	NM_006885.4(ZFHX3):c.7913C>T (p.Pro2638Leu)	ZFHX3, ZFHX3-AS1 (P1724L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193010	NM_006885.4(ZFHX3):c.788A>G (p.Asn263Ser)	ZFHX3 (N263S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193009	NM_006885.4(ZFHX3):c.6974A>C (p.Asn2325Thr)	ZFHX3, ZFHX3-AS1 (N2325T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193008	NM_006885.4(ZFHX3):c.6787G>A (p.Ala2263Thr)	ZFHX3, ZFHX3-AS1 (A1349T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193006	NM_006885.4(ZFHX3):c.6646A>G (p.Ile2216Val)	ZFHX3, ZFHX3-AS1 (I1302V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193005	NM_006885.4(ZFHX3):c.643T>C (p.Phe215Leu)	ZFHX3 (F215L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193004	NM_006885.4(ZFHX3):c.6247G>A (p.Val2083Met)	ZFHX3, ZFHX3-AS1 (V1169M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193000	NM_006885.4(ZFHX3):c.5760G>C (p.Glu1920Asp)	ZFHX3, ZFHX3-AS1 (E1006D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192999	NM_006885.4(ZFHX3):c.5565G>T (p.Gln1855His)	ZFHX3, ZFHX3-AS1 (Q1855H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192998	NM_006885.4(ZFHX3):c.5532G>C (p.Gln1844His)	ZFHX3, ZFHX3-AS1 (Q1844H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192997	NM_006885.4(ZFHX3):c.5434G>A (p.Glu1812Lys)	ZFHX3, ZFHX3-AS1 (E1812K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192995	NM_006885.4(ZFHX3):c.4645G>C (p.Val1549Leu)	ZFHX3, ZFHX3-AS1 (V1549L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192994	NM_006885.4(ZFHX3):c.4072T>G (p.Ser1358Ala)	ZFHX3, ZFHX3-AS1 (S1358A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192993	NM_006885.4(ZFHX3):c.3889C>A (p.Pro1297Thr)	ZFHX3, ZFHX3-AS1 (P383T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192992	NM_006885.4(ZFHX3):c.371G>A (p.Ser124Asn)	ZFHX3 (S124N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192991	NM_006885.4(ZFHX3):c.3640G>A (p.Ala1214Thr)	ZFHX3, ZFHX3-AS1 (A1214T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192990	NM_006885.4(ZFHX3):c.3584G>A (p.Arg1195His)	ZFHX3, ZFHX3-AS1 (R281H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192989	NM_006885.4(ZFHX3):c.3526G>A (p.Gly1176Arg)	ZFHX3 (G1176R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192987	NM_006885.4(ZFHX3):c.2944G>T (p.Asp982Tyr)	ZFHX3 (D68Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192985	NM_006885.4(ZFHX3):c.2668G>A (p.Gly890Arg)	ZFHX3 (G890R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192984	NM_006885.4(ZFHX3):c.2384C>T (p.Pro795Leu)	ZFHX3 (P795L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192983	NM_006885.4(ZFHX3):c.2282G>C (p.Gly761Ala)	ZFHX3 (G761A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192982	NM_006885.4(ZFHX3):c.2164G>A (p.Gly722Ser)	ZFHX3 (G722S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192981	NM_006885.4(ZFHX3):c.2091G>A (p.Pro697=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3192980	NM_006885.4(ZFHX3):c.2024A>G (p.Lys675Arg)	ZFHX3 (K675R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192979	NM_006885.4(ZFHX3):c.1610C>T (p.Pro537Leu)	ZFHX3 (P537L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192978	NM_006885.4(ZFHX3):c.1346G>C (p.Gly449Ala)	ZFHX3 (G449A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192976	NM_006885.4(ZFHX3):c.1145G>C (p.Gly382Ala)	ZFHX3 (G382A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192975	NM_006885.4(ZFHX3):c.10975G>A (p.Asp3659Asn)	ZFHX3, ZFHX3-AS1 (D2745N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3192973	NM_006885.4(ZFHX3):c.10841G>C (p.Arg3614Thr)	ZFHX3, ZFHX3-AS1 (R3614T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3192972	NM_006885.4(ZFHX3):c.10649C>T (p.Ser3550Leu)	ZFHX3, ZFHX3-AS1 (S2636L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192971	NM_006885.4(ZFHX3):c.10457C>T (p.Ser3486Phe)	ZFHX3, ZFHX3-AS1 (S3486F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192970	NM_006885.4(ZFHX3):c.10402C>T (p.Arg3468Cys)	ZFHX3, ZFHX3-AS1 (R2554C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192969	NM_006885.4(ZFHX3):c.10286G>A (p.Arg3429His)	ZFHX3, ZFHX3-AS1 (R2515H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192968	NM_006885.4(ZFHX3):c.10241C>A (p.Pro3414His)	ZFHX3, ZFHX3-AS1 (P3414H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063460	GRCh37/hg19 16q22.2-22.3(chr16:72515938-72912134)x1	ZFHX3	Copy number loss	not specified	GUncertain significance
Select item 3060785	NM_006885.4(ZFHX3):c.4929C>T (p.Ser1643=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3060596	NM_006885.4(ZFHX3):c.214T>G (p.Ser72Ala)	ZFHX3 (S72A)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3060370	NM_006885.4(ZFHX3):c.10542CGG[4] (p.Gly3527del)	ZFHX3, ZFHX3-AS1 (G2613del +1 more)	Microsatellite (inframe_deletion)	ZFHX3-related disorder	GBenign
Select item 3060173	NM_006885.4(ZFHX3):c.9879C>T (p.Ala3293=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3059894	NM_006885.4(ZFHX3):c.7155G>A (p.Pro2385=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3059882	NM_006885.4(ZFHX3):c.3968-7_3968-6dup	ZFHX3, ZFHX3-AS1	Duplication (intron variant)	ZFHX3-related disorder	GBenign
Select item 3059820	NM_006885.4(ZFHX3):c.8178T>C (p.Leu2726=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3059393	NM_006885.4(ZFHX3):c.1282A>C (p.Thr428Pro)	ZFHX3 (T428P)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3059241	NM_006885.4(ZFHX3):c.8823A>G (p.Gly2941=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3058928	NM_006885.4(ZFHX3):c.10558GGC[5] (p.Gly3525_Gly3527del)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe deletion)	ZFHX3-related disorder	GBenign
Select item 3058868	NM_006885.4(ZFHX3):c.185C>T (p.Ala62Val)	ZFHX3 (A62V)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3057238	NM_006885.4(ZFHX3):c.1848C>T (p.Phe616=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3057232	NM_006885.4(ZFHX3):c.1378G>C (p.Glu460Gln)	ZFHX3 (E460Q)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3057168	NM_006885.4(ZFHX3):c.5194CAA[9] (p.Gln1741del)	ZFHX3, ZFHX3-AS1 (Q1741del +1 more)	Microsatellite (inframe_deletion)	ZFHX3-related disorder	GBenign
Select item 3057090	NM_006885.4(ZFHX3):c.10558GGC[7] (p.Gly3527del)	ZFHX3, ZFHX3-AS1 (G2613del +1 more)	Microsatellite (inframe_deletion)	ZFHX3-related disorder	GBenign
Select item 3056905	NM_006885.4(ZFHX3):c.120G>A (p.Glu40=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3056902	NM_006885.4(ZFHX3):c.2916G>A (p.Ser972=)	ZFHX3	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3056720	NM_006885.4(ZFHX3):c.10558GGC[9] (p.Gly3527_Ser3528insGly)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe_insertion)	ZFHX3-related disorder	GBenign
Select item 3056706	NM_006885.4(ZFHX3):c.423G>A (p.Ala141=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3056548	NM_006885.4(ZFHX3):c.1135C>G (p.Leu379Val)	ZFHX3 (L379V)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3056525	NM_006885.4(ZFHX3):c.8316C>T (p.His2772=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3056424	NM_006885.4(ZFHX3):c.1776C>T (p.Asp592=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3056006	NM_006885.4(ZFHX3):c.320C>T (p.Pro107Leu)	ZFHX3 (P107L)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3055809	NM_006885.4(ZFHX3):c.339C>T (p.Ala113=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3055710	NM_006885.4(ZFHX3):c.3345C>T (p.Ser1115=)	ZFHX3	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GBenign
Select item 3055699	NM_006885.4(ZFHX3):c.5194CAA[12] (p.Gln1741_Ala1742insGlnGln)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe_insertion)	ZFHX3-related disorder	GBenign
Select item 3055601	NM_006885.4(ZFHX3):c.3664-6C>T	ZFHX3, ZFHX3-AS1	Single nucleotide variant (intron variant)	ZFHX3-related disorder	GBenign
Select item 3055382	NM_006885.4(ZFHX3):c.5026A>G (p.Ser1676Gly)	ZFHX3, ZFHX3-AS1 (S1676G +1 more)	Single nucleotide variant (missense variant)	ZFHX3-related disorder	GBenign
Select item 3055302	NM_006885.4(ZFHX3):c.337G>A (p.Ala113Thr)	ZFHX3 (A113T)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3054141	NM_006885.4(ZFHX3):c.10553_10554insTGG (p.Gly3527_Ser3528insGly)	ZFHX3, ZFHX3-AS1	Insertion (inframe insertion)	ZFHX3-related disorder	GLikely benign
Select item 3053773	NM_006885.4(ZFHX3):c.10542CGG[7] (p.Gly3527_Ser3528insGlyGly)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe insertion)	ZFHX3-related disorder	GLikely benign
Select item 3053402	NM_006885.4(ZFHX3):c.311C>T (p.Pro104Leu)	ZFHX3 (P104L)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GLikely benign
Select item 3053390	NM_006885.4(ZFHX3):c.1434AGAGGAGGAGGAAGA[1] (p.Glu483_Glu487del)	ZFHX3	Microsatellite (inframe deletion +1 more)	ZFHX3-related disorder	GLikely benign
Select item 3053230	NM_006885.4(ZFHX3):c.5194CAA[6] (p.Gln1738_Gln1741del)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe deletion)	ZFHX3-related disorder	GBenign
Select item 3053186	NM_006885.4(ZFHX3):c.5196A>G (p.Gln1732=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3052476	NM_006885.4(ZFHX3):c.9241T>C (p.Leu3081=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3051253	NM_006885.4(ZFHX3):c.2934G>A (p.Ala978=)	ZFHX3	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3051169	NM_006885.4(ZFHX3):c.10542CGG[6] (p.Gly3527_Ser3528insGly)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe insertion)	ZFHX3-related disorder	GLikely benign
Select item 3051150	NM_006885.4(ZFHX3):c.8346T>G (p.Gly2782=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3050988	NM_006885.4(ZFHX3):c.9483C>T (p.Ser3161=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3050798	NM_006885.4(ZFHX3):c.10794T>G (p.Pro3598=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	ZFHX3-related disorder	GLikely benign
Select item 3050722	NM_006885.4(ZFHX3):c.10519G>C (p.Gly3507Arg)	ZFHX3, ZFHX3-AS1 (G3507R +1 more)	Single nucleotide variant (missense variant)	ZFHX3-related disorder	GBenign
Select item 3050651	NM_006885.4(ZFHX3):c.54C>T (p.Ile18=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GLikely benign
Select item 3050182	NM_006885.4(ZFHX3):c.216C>G (p.Ser72=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GLikely benign
Select item 3050044	NM_006885.4(ZFHX3):c.9591GCA[10] (p.Gln3204_Pro3205insGlnGlnGln)	ZFHX3, ZFHX3-AS1	Microsatellite (inframe insertion)	ZFHX3-related disorder	GBenign
Select item 3049870	NM_006885.4(ZFHX3):c.10557_10568del (p.Gly3524_Gly3527del)	ZFHX3, ZFHX3-AS1	Deletion (inframe deletion)	ZFHX3-related disorder	GLikely benign
Select item 3049676	NM_006885.4(ZFHX3):c.222C>T (p.Pro74=)	ZFHX3	Single nucleotide variant (synonymous variant +1 more)	ZFHX3-related disorder	GBenign
Select item 3049574	NM_006885.4(ZFHX3):c.10440G>A (p.Ala3480=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3049193	NM_006885.4(ZFHX3):c.5160A>C (p.Ala1720=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3049155	NM_006885.4(ZFHX3):c.5714C>T (p.Pro1905Leu)	ZFHX3, ZFHX3-AS1 (P1905L +1 more)	Single nucleotide variant (missense variant)	ZFHX3-related disorder	GLikely benign
Select item 3048716	NM_006885.4(ZFHX3):c.6297G>A (p.Pro2099=)	ZFHX3, ZFHX3-AS1	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3048675	NM_006885.4(ZFHX3):c.3024C>T (p.His1008=)	ZFHX3	Single nucleotide variant (synonymous variant)	ZFHX3-related disorder	GLikely benign
Select item 3045442	NM_006885.4(ZFHX3):c.436A>G (p.Ser146Gly)	ZFHX3 (S146G)	Single nucleotide variant (missense variant +1 more)	ZFHX3-related disorder	GBenign

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