ZNF264[gene] - ClinVar

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

Search results

Items: 80

	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 151461	GRCh38/hg38 19q13.43(chr19:57167550-57236826)x1	AURKC, LOC130065162 +6 more	Copy number loss	See cases	GUncertain significance
Select item 3194756	NM_003417.5(ZNF264):c.26G>C (p.Arg9Pro)	LOC130065167, ZNF264 (R9P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391343	NM_003417.5(ZNF264):c.55G>A (p.Val19Met)	ZNF264 (V19M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194760	NM_003417.5(ZNF264):c.71C>G (p.Thr24Ser)	ZNF264 (T24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194763	NM_003417.5(ZNF264):c.78G>T (p.Glu26Asp)	ZNF264 (E26D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283799	NM_003417.5(ZNF264):c.85G>A (p.Gly29Arg)	ZNF264 (G29R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194751	NM_003417.5(ZNF264):c.107G>A (p.Arg36Gln)	ZNF264 (R36Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539537	NM_003417.5(ZNF264):c.195C>A (p.His65Gln)	ZNF264 (H65Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3335288	NM_003417.5(ZNF264):c.205G>A (p.Gly69Arg)	ZNF264 (G69R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549300	NM_003417.5(ZNF264):c.304G>A (p.Ala102Thr)	ZNF264 (A102T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335290	NM_003417.5(ZNF264):c.305C>A (p.Ala102Asp)	ZNF264 (A102D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488562	NM_003417.5(ZNF264):c.305C>T (p.Ala102Val)	ZNF264 (A102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389353	NM_003417.5(ZNF264):c.420C>G (p.Phe140Leu)	ZNF264 (F140L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2209609	NM_003417.5(ZNF264):c.470A>G (p.Glu157Gly)	ZNF264 (E157G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618829	NM_003417.5(ZNF264):c.562T>G (p.Cys188Gly)	ZNF264 (C188G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194757	NM_003417.5(ZNF264):c.598G>A (p.Glu200Lys)	ZNF264 (E200K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194758	NM_003417.5(ZNF264):c.661C>T (p.His221Tyr)	ZNF264 (H221Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335291	NM_003417.5(ZNF264):c.671T>C (p.Ile224Thr)	ZNF264 (I224T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335287	NM_003417.5(ZNF264):c.697T>G (p.Cys233Gly)	ZNF264 (C233G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483222	NM_003417.5(ZNF264):c.722T>G (p.Ile241Ser)	ZNF264 (I241S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194761	NM_003417.5(ZNF264):c.736C>G (p.Leu246Val)	ZNF264 (L246V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194762	NM_003417.5(ZNF264):c.784A>T (p.Met262Leu)	ZNF264 (M262L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194764	NM_003417.5(ZNF264):c.856C>G (p.Pro286Ala)	ZNF264 (P286A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335289	NM_003417.5(ZNF264):c.877G>A (p.Gly293Arg)	ZNF264 (G293R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391241	NM_003417.5(ZNF264):c.908T>A (p.Val303Asp)	ZNF264 (V303D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386858	NM_003417.5(ZNF264):c.974G>A (p.Arg325Gln)	ZNF264 (R325Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194749	NM_003417.5(ZNF264):c.1016G>C (p.Gly339Ala)	ZNF264 (G339A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194750	NM_003417.5(ZNF264):c.1022A>C (p.Asn341Thr)	ZNF264 (N341T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382203	NM_003417.5(ZNF264):c.1028A>G (p.Tyr343Cys)	ZNF264 (Y343C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524640	NM_003417.5(ZNF264):c.1102G>A (p.Glu368Lys)	ZNF264 (E368K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399700	NM_003417.5(ZNF264):c.1112A>G (p.Tyr371Cys)	ZNF264 (Y371C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524796	NM_003417.5(ZNF264):c.1120A>G (p.Ser374Gly)	ZNF264 (S374G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479011	NM_003417.5(ZNF264):c.1138T>G (p.Phe380Val)	ZNF264 (F380V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335286	NM_003417.5(ZNF264):c.1148G>C (p.Ser383Thr)	ZNF264 (S383T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589889	NM_003417.5(ZNF264):c.1160T>A (p.Ile387Asn)	ZNF264 (I387N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194752	NM_003417.5(ZNF264):c.1231C>G (p.Arg411Gly)	ZNF264 (R411G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269589	NM_003417.5(ZNF264):c.1232G>A (p.Arg411Gln)	ZNF264 (R411Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520731	NM_003417.5(ZNF264):c.1336A>G (p.Lys446Glu)	ZNF264 (K446E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242292	NM_003417.5(ZNF264):c.1340G>A (p.Arg447Lys)	ZNF264 (R447K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543484	NM_003417.5(ZNF264):c.1360C>G (p.Pro454Ala)	ZNF264 (P454A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250373	NM_003417.5(ZNF264):c.1400G>A (p.Arg467Gln)	ZNF264 (R467Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344635	NM_003417.5(ZNF264):c.1414C>T (p.Arg472Cys)	ZNF264 (R472C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355985	NM_003417.5(ZNF264):c.1427T>C (p.Ile476Thr)	ZNF264 (I476T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472576	NM_003417.5(ZNF264):c.1451A>T (p.Glu484Val)	ZNF264 (E484V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3039214	NM_003417.5(ZNF264):c.1456G>A (p.Val486Met)	ZNF264 (V486M)	Single nucleotide variant (missense variant)	ZNF264-related disorder	GLikely benign
Select item 2364097	NM_003417.5(ZNF264):c.1487C>T (p.Ser496Leu)	ZNF264 (S496L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372689	NM_003417.5(ZNF264):c.1496C>T (p.Thr499Met)	ZNF264 (T499M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518616	NM_003417.5(ZNF264):c.1504A>C (p.Lys502Gln)	ZNF264 (K502Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3194755	NM_003417.5(ZNF264):c.1517G>A (p.Ser506Asn)	ZNF264 (S506N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243137	NM_003417.5(ZNF264):c.1522G>C (p.Glu508Gln)	ZNF264 (E508Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529365	NM_003417.5(ZNF264):c.1567A>T (p.Ser523Cys)	ZNF264 (S523C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343139	NM_003417.5(ZNF264):c.1616A>G (p.Tyr539Cys)	ZNF264 (Y539C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589568	NM_003417.5(ZNF264):c.1664C>T (p.Thr555Ile)	ZNF264 (T555I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304274	NM_003417.5(ZNF264):c.1673A>G (p.Gln558Arg)	ZNF264 (Q558R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370323	NM_003417.5(ZNF264):c.1739A>G (p.Gln580Arg)	ZNF264 (Q580R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274485	NM_003417.5(ZNF264):c.1759G>C (p.Glu587Gln)	ZNF264 (E587Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335285	NM_003417.5(ZNF264):c.1780T>A (p.Phe594Ile)	ZNF264 (F594I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225253	NM_003417.5(ZNF264):c.1804A>G (p.Asn602Asp)	ZNF264 (N602D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335292	NM_003417.5(ZNF264):c.1868A>G (p.Gln623Arg)	ZNF264 (Q623R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 816097	GRCh37/hg19 19q13.43(chr19:57671695-57745390)x1	ZNF264, DUXA +1 more	Copy number loss	not provided	GUncertain significance
Select item 685831	GRCh37/hg19 19q13.43(chr19:57590808-57745390)x3	AURKC, DUXA +3 more	Copy number gain	not provided	GUncertain significance
Select item 685408	GRCh37/hg19 19q13.43(chr19:57718739-57760953)x1	AURKC, ZNF264 +1 more	Copy number loss	not provided	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 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: 80