ZFP28[gene] - ClinVar

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Items: 85

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 more	Copy number gain	See cases	GPathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065034, LOC130065035 +761 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 153721	GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	A1BG, A1BG-AS1 +547 more	Copy number gain	See cases	GPathogenic
Select item 144762	GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	SSC5D, SYT5 +553 more	Copy number gain	See cases	GPathogenic
Select item 144709	GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	TMC4, TMEM150B +537 more	Copy number gain	See cases	GPathogenic
Select item 154108	GRCh38/hg38 19q13.42-13.43(chr19:55037146-56982033)x3	BRSK1, C19orf85 +196 more	Copy number gain	See cases	GUncertain significance
Select item 149081	GRCh38/hg38 19q13.42-13.43(chr19:55048514-56972458)x3	BRSK1, C19orf85 +194 more	Copy number gain	See cases	GLikely pathogenic
Select item 145961	GRCh38/hg38 19q13.42-13.43(chr19:55550939-57031576)x1	CCDC106, EDDM13 +106 more	Copy number loss	See cases	GLikely pathogenic
Select item 153557	GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3	A1BG, A1BG-AS1 +179 more	Copy number gain	See cases	GUncertain significance
Select item 59128	GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3	A1BG, A1BG-AS1 +215 more	Copy number gain	See cases	GPathogenic
Select item 3334447	NM_020828.2(ZFP28):c.5G>C (p.Arg2Pro)	ZFP28 (R2P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286970	NM_020828.2(ZFP28):c.8G>T (p.Gly3Val)	ZFP28 (G3V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521478	NM_020828.2(ZFP28):c.14C>A (p.Ala5Glu)	ZFP28 (A5E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299049	NM_020828.2(ZFP28):c.14C>T (p.Ala5Val)	ZFP28 (A5V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411375	NM_020828.2(ZFP28):c.35C>G (p.Pro12Arg)	ZFP28 (P12R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314536	NM_020828.2(ZFP28):c.40C>A (p.Pro14Thr)	ZFP28 (P14T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612935	NM_020828.2(ZFP28):c.41C>A (p.Pro14Gln)	ZFP28 (P14Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375876	NM_020828.2(ZFP28):c.58G>A (p.Ala20Thr)	ZFP28 (A20T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334446	NM_020828.2(ZFP28):c.62C>T (p.Pro21Leu)	ZFP28 (P21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334453	NM_020828.2(ZFP28):c.65G>A (p.Arg22His)	ZFP28 (R22H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193102	NM_020828.2(ZFP28):c.68C>T (p.Thr23Ile)	ZFP28 (T23I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408737	NM_020828.2(ZFP28):c.68C>G (p.Thr23Arg)	ZFP28 (T23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3338593	NM_020828.2(ZFP28):c.74C>G (p.Pro25Arg)	ZFP28 (P25R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2518905	NM_020828.2(ZFP28):c.143G>C (p.Arg48Pro)	ZFP28 (R48P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334452	NM_020828.2(ZFP28):c.157C>T (p.Leu53Phe)	ZFP28 (L53F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309586	NM_020828.2(ZFP28):c.191C>A (p.Thr64Lys)	ZFP28 (T64K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377890	NM_020828.2(ZFP28):c.196C>T (p.Pro66Ser)	ZFP28 (P66S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597253	NM_020828.2(ZFP28):c.214C>T (p.Pro72Ser)	ZFP28 (P72S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278913	NM_020828.2(ZFP28):c.226A>G (p.Thr76Ala)	ZFP28 (T76A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354113	NM_020828.2(ZFP28):c.487A>T (p.Thr163Ser)	LOC126862942, ZFP28 +1 more (T163S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343480	NM_020828.2(ZFP28):c.577G>A (p.Glu193Lys)	ZFP28, ZNF470-DT (E193K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314590	NM_020828.2(ZFP28):c.611G>C (p.Arg204Thr)	ZFP28, ZNF470-DT (R204T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247643	NM_020828.2(ZFP28):c.660T>G (p.Asp220Glu)	ZFP28, ZNF470-DT (D220E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193101	NM_020828.2(ZFP28):c.670C>G (p.Leu224Val)	ZFP28, ZNF470-DT (L224V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334449	NM_020828.2(ZFP28):c.686C>T (p.Pro229Leu)	ZFP28, ZNF470-DT (P229L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193103	NM_020828.2(ZFP28):c.693G>C (p.Leu231Phe)	ZFP28, ZNF470-DT (L231F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398999	NM_020828.2(ZFP28):c.724C>T (p.Arg242Cys)	ZFP28, ZNF470-DT (R242C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193104	NM_020828.2(ZFP28):c.738C>G (p.His246Gln)	ZFP28, ZNF470-DT (H246Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350499	NM_020828.2(ZFP28):c.914A>T (p.His305Leu)	ZFP28, ZNF470-DT (H305L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333062	NM_020828.2(ZFP28):c.917A>G (p.Glu306Gly)	ZFP28, ZNF470-DT (E306G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334451	NM_020828.2(ZFP28):c.931T>C (p.Phe311Leu)	ZFP28, ZNF470-DT (F311L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334454	NM_020828.2(ZFP28):c.961G>C (p.Val321Leu)	ZFP28, ZNF470-DT (V321L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321352	NM_020828.2(ZFP28):c.1013A>G (p.Asn338Ser)	ZFP28, ZNF470-DT (N338S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621872	NM_020828.2(ZFP28):c.1018G>A (p.Asp340Asn)	ZFP28, ZNF470-DT (D340N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232218	NM_020828.2(ZFP28):c.1028A>C (p.Tyr343Ser)	ZFP28, ZNF470-DT (Y343S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376536	NM_020828.2(ZFP28):c.1100C>T (p.Thr367Ile)	ZFP28, ZNF470-DT (T367I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214111	NM_020828.2(ZFP28):c.1162T>G (p.Ser388Ala)	ZFP28, ZNF470-DT (S388A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334448	NM_020828.2(ZFP28):c.1211G>A (p.Ser404Asn)	ZFP28, ZNF470-DT (S404N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3334450	NM_020828.2(ZFP28):c.1355A>G (p.Glu452Gly)	ZFP28, ZNF470-DT (E452G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389147	NM_020828.2(ZFP28):c.1430A>G (p.Glu477Gly)	ZFP28, ZNF470-DT (E477G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467228	NM_020828.2(ZFP28):c.1493A>G (p.Tyr498Cys)	LOC126862943, ZFP28 +1 more (Y498C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296788	NM_020828.2(ZFP28):c.1669G>A (p.Gly557Arg)	LOC126862943, ZFP28 +1 more (G557R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234521	NM_020828.2(ZFP28):c.1693G>A (p.Val565Ile)	LOC126862943, ZFP28 +1 more (V565I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334455	NM_020828.2(ZFP28):c.1831C>A (p.His611Asn)	LOC126862943, ZFP28 +1 more (H611N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238781	NM_020828.2(ZFP28):c.1840G>A (p.Glu614Lys)	LOC126862943, ZFP28 +1 more (E614K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193097	NM_020828.2(ZFP28):c.1909A>G (p.Arg637Gly)	LOC126862943, ZFP28 +1 more (R637G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519698	NM_020828.2(ZFP28):c.1936G>A (p.Glu646Lys)	LOC126862943, ZFP28 +1 more (E646K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214112	NM_020828.2(ZFP28):c.2112G>C (p.Met704Ile)	LOC126862943, ZFP28 +1 more (M704I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2392906	NM_020828.2(ZFP28):c.2228C>T (p.Ser743Phe)	LOC126862943, ZFP28 +1 more (S743F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333467	NM_020828.2(ZFP28):c.2267C>G (p.Pro756Arg)	LOC126862943, ZFP28 +1 more (P756R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193098	NM_020828.2(ZFP28):c.2527C>T (p.Pro843Ser)	LOC126862943, ZFP28 +1 more (P843S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193099	NM_020828.2(ZFP28):c.2566C>T (p.Pro856Ser)	LOC126862943, ZFP28 +1 more (P856S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062375	GRCh37/hg19 19q13.42-13.43(chr19:56080158-57672397)x1	CCDC106, DUXA +36 more	Copy number loss	not specified	GUncertain significance
Select item 2684894	GRCh37/hg19 19q13.43(chr19:56949121-57419586)x3	PEG3, SMIM17 +8 more	Copy number gain	not provided	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 1526672	GRCh37/hg19 19q13.43(chr19:56332200-57126728)	GALP, NLRP11 +15 more	Copy number gain	not specified	GUncertain significance
Select item 980775	GRCh37/hg19 19q13.43(chr19:56792817-57074724)x3	ZFP28, ZNF471 +3 more	Copy number gain	not provided	GUncertain significance
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	PPP1R15A, PPP2R1A +308 more	Copy number gain	not provided	GPathogenic
Select item 816096	GRCh37/hg19 19q13.43(chr19:56788816-57277655)x3	SMIM17, ZNF71 +8 more	Copy number gain	not provided	GLikely benign
Select item 564606	GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	ZNF548, ZNF549 +157 more	Copy number gain	not provided	GPathogenic
Select item 564598	GRCh37/hg19 19q13.43(chr19:56565455-57401997)x1	ZNF667, ZNF471 +16 more	Copy number loss	not provided	GUncertain significance
Select item 443658	GRCh37/hg19 19q13.42-13.43(chr19:55844155-57408007)x3	CCDC106, COX6B2 +47 more	Copy number gain	See cases	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443202	GRCh37/hg19 19q13.42-13.43(chr19:55549385-57489784)x3	BRSK1, CCDC106 +61 more	Copy number gain	See cases	GUncertain significance
Select item 442403	GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3	A1BG, AURKC +64 more	Copy number gain	See cases	GUncertain significance
Select item 442366	GRCh37/hg19 19q13.42-13.43(chr19:56212463-57191708)x3	GALP, NLRP11 +21 more	Copy number gain	See cases	GUncertain significance
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 394098	GRCh37/hg19 19q13.43(chr19:56874577-57183789)x3	SMIM17, ZFP28 +8 more	Copy number gain	See cases	GUncertain significance
Select item 221405	GRCh37/hg19 19q13.42-13.43(chr19:56200298-57654005)x1	NLRP5, NLRP8 +26 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221354	chr19:56133299..57648277 complex variant	NLRP4, CCDC106 +31 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 85