ZNF304[gene] - ClinVar

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Items: 59

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	ZBTB45, ZFP28 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064933, LOC130064934 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	MIR10394, MIR125A +806 more	Copy number gain	See cases	GPathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	A1BG, A1BG-AS1 +782 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LILRA4, LILRA5 +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 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 2377254	NM_020657.4(ZNF304):c.49G>A (p.Glu17Lys)	ZNF304 (E17K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335952	NM_020657.4(ZNF304):c.73C>T (p.Arg25Trp)	ZNF304 (R25W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327264	NM_020657.4(ZNF304):c.97G>C (p.Glu33Gln)	ZNF304 (E33Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249030	NM_020657.4(ZNF304):c.154A>T (p.Thr52Ser)	ZNF304 (T52S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2273954	NM_020657.4(ZNF304):c.182A>G (p.His61Arg)	ZNF304 (H108R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195050	NM_020657.4(ZNF304):c.206T>C (p.Val69Ala)	ZNF304 (V27A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343837	NM_020657.4(ZNF304):c.208T>G (p.Ser70Ala)	ZNF304 (S70A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251176	NM_020657.4(ZNF304):c.389C>T (p.Ala130Val)	ZNF304 (A38V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608315	NM_020657.4(ZNF304):c.442G>A (p.Asp148Asn)	ZNF304 (D106N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195052	NM_020657.4(ZNF304):c.503C>T (p.Thr168Met)	ZNF304 (T76M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195051	NM_020657.4(ZNF304):c.503C>A (p.Thr168Lys)	ZNF304 (T126K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358386	NM_020657.4(ZNF304):c.529C>A (p.Pro177Thr)	ZNF304 (P224T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195053	NM_020657.4(ZNF304):c.536G>T (p.Ser179Ile)	ZNF304 (S226I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319063	NM_020657.4(ZNF304):c.558G>C (p.Gln186His)	ZNF304 (Q94H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204960	NM_020657.4(ZNF304):c.572G>A (p.Arg191Lys)	ZNF304 (R99K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287898	NM_020657.4(ZNF304):c.574G>A (p.Val192Met)	ZNF304 (V192M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351080	NM_020657.4(ZNF304):c.593C>T (p.Thr198Ile)	ZNF304 (T198I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195054	NM_020657.4(ZNF304):c.650A>G (p.Tyr217Cys)	ZNF304 (Y264C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271998	NM_020657.4(ZNF304):c.676G>A (p.Gly226Ser)	ZNF304 (G184S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2517311	NM_020657.4(ZNF304):c.767G>T (p.Cys256Phe)	ZNF304 (C164F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195055	NM_020657.4(ZNF304):c.776T>C (p.Val259Ala)	ZNF304 (V217A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326118	NM_020657.4(ZNF304):c.780C>A (p.Phe260Leu)	ZNF304 (F218L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477561	NM_020657.4(ZNF304):c.805C>T (p.His269Tyr)	ZNF304 (H269Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490178	NM_020657.4(ZNF304):c.809G>A (p.Arg270Lys)	ZNF304 (R270K +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2232408	NM_020657.4(ZNF304):c.925T>G (p.Cys309Gly)	ZNF304 (C217G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458321	NM_020657.4(ZNF304):c.950G>C (p.Ser317Thr)	ZNF304 (S364T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195041	NM_020657.4(ZNF304):c.1016A>C (p.Glu339Ala)	ZNF304 (E247A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650569	NM_020657.4(ZNF304):c.1119C>T (p.Ser373=)	ZNF304	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3195042	NM_020657.4(ZNF304):c.1342G>A (p.Val448Met)	ZNF304 (V448M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161734	NM_020657.4(ZNF304):c.1400T>A (p.Ile467Lys)	ZNF304 (I467K +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 3195043	NM_020657.4(ZNF304):c.1434T>G (p.Ser478Arg)	ZNF304 (S386R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195044	NM_020657.4(ZNF304):c.1447G>T (p.Ala483Ser)	ZNF304 (A441S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195045	NM_020657.4(ZNF304):c.1568G>T (p.Arg523Ile)	ZNF304 (R481I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195046	NM_020657.4(ZNF304):c.1600A>G (p.Asn534Asp)	ZNF304 (N442D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213236	NM_020657.4(ZNF304):c.1601A>G (p.Asn534Ser)	ZNF304 (N581S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3195047	NM_020657.4(ZNF304):c.1629C>G (p.Asn543Lys)	ZNF304 (N451K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195048	NM_020657.4(ZNF304):c.1793G>T (p.Arg598Leu)	ZNF304 (R506L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539189	NM_020657.4(ZNF304):c.1822G>T (p.Val608Phe)	ZNF304 (V516F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381699	NM_020657.4(ZNF304):c.1940G>C (p.Ser647Thr)	ZNF304 (S555T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195049	NM_020657.4(ZNF304):c.1961C>A (p.Ala654Glu)	ZNF304 (A562E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 564590	GRCh37/hg19 19q13.43(chr19:57718739-58058739)x1	VN1R1, AURKC +14 more	Copy number loss	not provided	GUncertain significance
Select item 560105	Single allele	ZNF805, ZNF17 +11 more	Duplication	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 442403	GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3	A1BG, AURKC +64 more	Copy number gain	See cases	GUncertain significance
Select item 395251	GRCh37/hg19 19q13.43(chr19:57831925-57862899)x3	ZNF304, ZNF543	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

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Items: 59