ZNF304[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 64

	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 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 3335429	NM_020657.4(ZNF304):c.672T>G (p.Ser224Arg)	ZNF304 (S132R +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 3335426	NM_020657.4(ZNF304):c.1183G>A (p.Glu395Lys)	ZNF304 (E395K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335423	NM_020657.4(ZNF304):c.1220T>C (p.Ile407Thr)	ZNF304 (I407T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335428	NM_020657.4(ZNF304):c.1312C>G (p.Arg438Gly)	ZNF304 (R346G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3335427	NM_020657.4(ZNF304):c.1448C>A (p.Ala483Asp)	ZNF304 (A391D +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)	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 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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 64