"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZFHX4"[ge - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058764	NM_024721.5(ZFHX4):c.159G>C (p.Thr53=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3037425	NM_024721.5(ZFHX4):c.196G>C (p.Val66Leu)	ZFHX4 (V66L)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 2658657	NM_024721.5(ZFHX4):c.196G>A (p.Val66Ile)	ZFHX4 (V66I)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3053194	NM_024721.5(ZFHX4):c.234G>A (p.Lys78=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3057594	NM_024721.5(ZFHX4):c.447G>A (p.Gly149=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 734150	NM_024721.5(ZFHX4):c.597A>T (p.Ser199=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition +1 more	GBenign/Likely benign
Select item 3043988	NM_024721.5(ZFHX4):c.609A>G (p.Lys203=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3041201	NM_024721.5(ZFHX4):c.1032T>C (p.Val344=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3049996	NM_024721.5(ZFHX4):c.1119C>T (p.Asp373=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 724846	NM_024721.5(ZFHX4):c.1177G>C (p.Glu393Gln)	ZFHX4 (E393Q)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3050045	NM_024721.5(ZFHX4):c.1413T>C (p.Asp471=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3050059	NM_024721.5(ZFHX4):c.1475C>T (p.Thr492Ile)	ZFHX4 (T492I)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 2636222	NM_024721.5(ZFHX4):c.2883del (p.Cys962fs)	ZFHX4 (C936fs +1 more)	Deletion (frameshift variant)	ZFHX4-related condition	GUncertain significance
Select item 2658661	NM_024721.5(ZFHX4):c.3006C>T (p.Asn1002=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3040344	NM_024721.5(ZFHX4):c.3069C>T (p.His1023=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3035213	NM_024721.5(ZFHX4):c.3075G>A (p.Ala1025=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 715619	NM_024721.5(ZFHX4):c.3150C>T (p.Ala1050=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3058442	NM_024721.5(ZFHX4):c.3174C>T (p.Val1058=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 2375459	NM_024721.5(ZFHX4):c.3445G>A (p.Glu1149Lys)	ZFHX4 (E1123K +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3038793	NM_024721.5(ZFHX4):c.3550G>C (p.Ala1184Pro)	ZFHX4 (A1158P +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 2369471	NM_024721.5(ZFHX4):c.3722C>T (p.Ser1241Leu)	ZFHX4 (S1241L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2658663	NM_024721.5(ZFHX4):c.3726G>T (p.Val1242=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3037269	NM_024721.5(ZFHX4):c.3817C>T (p.Pro1273Ser)	ZFHX4 (P1247S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 2636634	NM_024721.5(ZFHX4):c.3853G>C (p.Val1285Leu)	ZFHX4 (V1259L +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GUncertain significance
Select item 3043459	NM_024721.5(ZFHX4):c.3964+6C>A	ZFHX4	Single nucleotide variant (intron variant)	ZFHX4-related condition	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 condition	GLikely benign
Select item 3043055	NM_024721.5(ZFHX4):c.4419C>T (p.Ser1473=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	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 condition	GLikely benign
Select item 3053820	NM_024721.5(ZFHX4):c.4700A>G (p.His1567Arg)	ZFHX4 (H1541R +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 784131	NM_024721.5(ZFHX4):c.4916C>T (p.Ala1639Val)	ZFHX4 (A1639V)	Single nucleotide variant (missense variant)	ZFHX4-related condition +1 more	GBenign
Select item 3043520	NM_024721.5(ZFHX4):c.4945A>T (p.Met1649Leu)	ZFHX4 (M1623L +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GLikely benign
Select item 720428	NM_024721.5(ZFHX4):c.5316C>G (p.Gly1772=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition +1 more	GBenign/Likely benign
Select item 2658667	NM_024721.5(ZFHX4):c.5361C>T (p.His1787=)	ZFHX4	Single nucleotide variant (synonymous variant)	not provided +1 more	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 condition	GBenign
Select item 3034731	NM_024721.5(ZFHX4):c.5682C>A (p.Ser1894=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3038664	NM_024721.5(ZFHX4):c.5820C>T (p.Gly1940=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3044841	NM_024721.5(ZFHX4):c.6089C>T (p.Thr2030Met)	ZFHX4 (T2004M +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 3040704	NM_024721.5(ZFHX4):c.6103C>T (p.Leu2035=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3038466	NM_024721.5(ZFHX4):c.6141A>C (p.Pro2047=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3053805	NM_024721.5(ZFHX4):c.6147T>A (p.Pro2049=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3060954	NM_024721.5(ZFHX4):c.6708C>T (p.Tyr2236=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3056770	NM_024721.5(ZFHX4):c.6793C>T (p.Leu2265=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3031806	NM_024721.5(ZFHX4):c.6964C>T (p.Pro2322Ser)	ZFHX4 (P2296S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GLikely benign
Select item 3038346	NM_024721.5(ZFHX4):c.7179A>G (p.Pro2393=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3042716	NM_024721.5(ZFHX4):c.7581G>A (p.Pro2527=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3052499	NM_024721.5(ZFHX4):c.7749C>T (p.Asp2583=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 2631236	NM_024721.5(ZFHX4):c.7918C>G (p.Arg2640Gly)	ZFHX4 (R2614G +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GUncertain significance
Select item 3056977	NM_024721.5(ZFHX4):c.8772T>C (p.Asn2924=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3050099	NM_024721.5(ZFHX4):c.9133C>A (p.Arg3045=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GBenign
Select item 3056218	NM_024721.5(ZFHX4):c.9355C>A (p.Pro3119Thr)	ZFHX4 (P3093T +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GBenign
Select item 3045955	NM_024721.5(ZFHX4):c.9400G>A (p.Gly3134Ser)	ZFHX4 (G3108S +1 more)	Single nucleotide variant (missense variant)	ZFHX4-related condition	GLikely benign
Select item 3048203	NM_024721.5(ZFHX4):c.9636C>T (p.Pro3212=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3051212	NM_024721.5(ZFHX4):c.9783G>A (p.Gln3261=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	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 condition	GLikely benign
Select item 3057284	NM_024721.5(ZFHX4):c.10182C>T (p.Tyr3394=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3058384	NM_024721.5(ZFHX4):c.10200G>A (p.Lys3400=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3042101	NM_024721.5(ZFHX4):c.10461T>C (p.Val3487=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign
Select item 3045184	NM_024721.5(ZFHX4):c.10623C>G (p.Pro3541=)	ZFHX4	Single nucleotide variant (synonymous variant)	ZFHX4-related condition	GLikely benign

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Items: 58