ClinVar for Gene (Select 147658) - ClinVar

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

Links from Gene

Items: 57

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258582	NM_001143938.3(ZNF534):c.1234T>C (p.Cys412Arg)	ZNF534 (C425R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258581	NM_001143938.3(ZNF534):c.1802C>A (p.Thr601Asn)	ZNF534 (T573N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258580	NM_001143938.3(ZNF534):c.578A>G (p.Lys193Arg)	ZNF534 (K193R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258579	NM_001143938.3(ZNF534):c.1057C>T (p.Pro353Ser)	ZNF534 (P366S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258578	NM_001143938.3(ZNF534):c.217G>A (p.Val73Met)	ZNF534 (V45M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196530	NM_001143938.3(ZNF534):c.934A>G (p.Ser312Gly)	ZNF534 (S325G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196529	NM_001143938.3(ZNF534):c.1964T>C (p.Ile655Thr)	ZNF534 (I655T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196528	NM_001143938.3(ZNF534):c.1957T>G (p.Cys653Gly)	ZNF534 (C653G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196527	NM_001143938.3(ZNF534):c.1859G>A (p.Arg620His)	ZNF534 (R633H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3196526	NM_001143938.3(ZNF534):c.1678A>C (p.Ser560Arg)	ZNF534 (S573R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196524	NM_001143938.3(ZNF534):c.1223G>A (p.Arg408Lys)	ZNF534 (R421K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3196523	NM_001143938.3(ZNF534):c.1135G>A (p.Glu379Lys)	ZNF534 (E379K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196522	NM_001143938.3(ZNF534):c.1120A>G (p.Lys374Glu)	ZNF534 (K387E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196521	NM_001143938.3(ZNF534):c.999G>C (p.Lys333Asn)	ZNF534 (K333N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	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 2681674	NM_001143938.3(ZNF534):c.785A>G (p.Lys262Arg)	ZNF534 (K234R +2 more)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2650394	NM_001143938.3(ZNF534):c.1698G>A (p.Ala566=)	ZNF534	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650393	NM_001143938.3(ZNF534):c.1497T>C (p.Cys499=)	ZNF534	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2608388	NM_001143938.3(ZNF534):c.1438A>G (p.Asn480Asp)	ZNF534 (N493D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595735	NM_001143938.3(ZNF534):c.1846A>C (p.Ser616Arg)	ZNF534 (S588R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551818	NM_001143938.3(ZNF534):c.1475A>C (p.Lys492Thr)	ZNF534 (K464T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546364	NM_001143938.3(ZNF534):c.1511G>A (p.Arg504His)	ZNF534 (R476H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540845	NM_001143938.3(ZNF534):c.649A>G (p.Ser217Gly)	ZNF534 (S230G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535833	NM_001143938.3(ZNF534):c.1898C>T (p.Pro633Leu)	ZNF534 (P605L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533879	NM_001143938.3(ZNF534):c.56A>C (p.Gln19Pro)	ZNF534 (Q19P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487193	NM_001143938.3(ZNF534):c.1721G>A (p.Gly574Glu)	ZNF534 (G546E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486523	NM_001143938.3(ZNF534):c.142+15C>A	ZNF534 (R53S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480319	NM_001143938.3(ZNF534):c.342G>T (p.Gln114His)	ZNF534 (Q114H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402895	NM_001143938.3(ZNF534):c.1697C>T (p.Ala566Val)	ZNF534 (A538V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390945	NM_001143938.3(ZNF534):c.907T>C (p.Cys303Arg)	ZNF534 (C303R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350326	NM_001143938.3(ZNF534):c.1648T>C (p.Tyr550His)	ZNF534 (Y522H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344350	NM_001143938.3(ZNF534):c.565A>C (p.Asn189His)	ZNF534 (N189H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319709	NM_001143938.3(ZNF534):c.1316A>G (p.Glu439Gly)	ZNF534 (E411G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295342	NM_001143938.3(ZNF534):c.142G>C (p.Gly48Arg)	ZNF534 (D48H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294703	NM_001143938.3(ZNF534):c.806C>G (p.Pro269Arg)	ZNF534 (P282R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242647	NM_001143938.3(ZNF534):c.37G>A (p.Val13Met)	ZNF534 (V13M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229466	NM_001143938.3(ZNF534):c.553C>G (p.Pro185Ala)	ZNF534 (P157A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217173	NM_001143938.3(ZNF534):c.1961G>A (p.Ser654Asn)	ZNF534 (S626N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214962	NM_001143938.3(ZNF534):c.310T>C (p.Ser104Pro)	ZNF534 (S117P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2214961	NM_001143938.3(ZNF534):c.1159T>A (p.Cys387Ser)	ZNF534 (C387S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208084	NM_001143938.3(ZNF534):c.239A>G (p.Asp80Gly)	ZNF534 (D52G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1526670	GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	FPR3, ZNF577 +115 more	Copy number gain	not specified	GLikely pathogenic
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 972980	GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	GRIN2D, GRWD1 +228 more	Copy number gain	not provided	Gnot provided
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	C5AR1, C5AR2 +293 more	Copy number gain	not provided	GPathogenic
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 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 253924	GRCh37/hg19 19q13.41(chr19:52825019-53017595)x1	ZNF480, ZNF528 +5 more	Copy number loss	See cases	GUncertain significance
Select item 161531	NM_001143938.3(ZNF534):c.13C>A (p.Gln5Lys)	ZNF534 (Q5K +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
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 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 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 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 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 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 57