ClinVar for Gene (Select 147658) - ClinVar

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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 (intron 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

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Links from Gene

Items: 57