ZNF419[gene] - ClinVar

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Items: 61

	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 3335711	NM_024691.4(ZNF419):c.14C>T (p.Ala5Val)	ZNF419 (A5V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335886	NM_024691.4(ZNF419):c.19A>G (p.Arg7Gly)	ZNF419 (R7G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161512	NM_024691.4(ZNF419):c.73G>T (p.Gly25Cys)	ZNF419 (G26C +3 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 2301782	NM_024691.4(ZNF419):c.88G>C (p.Glu30Gln)	ZNF419 (E17Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527827	NM_024691.4(ZNF419):c.91G>T (p.Asp31Tyr)	ZNF419 (D31Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335709	NM_024691.4(ZNF419):c.129G>T (p.Leu43Phe)	ZNF419 (L43F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335707	NM_024691.4(ZNF419):c.139G>A (p.Ala47Thr)	ZNF419 (A47T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2236967	NM_024691.4(ZNF419):c.155A>C (p.Tyr52Ser)	ZNF419 (Y39S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195643	NM_024691.4(ZNF419):c.166A>G (p.Met56Val)	ZNF419 (M56V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357887	NM_024691.4(ZNF419):c.221A>G (p.His74Arg)	ZNF419 (H61R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517186	NM_024691.4(ZNF419):c.293C>T (p.Pro98Leu)	ZNF419 (P86L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195644	NM_024691.4(ZNF419):c.331C>T (p.Pro111Ser)	ZNF419 (P99S +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286046	NM_024691.4(ZNF419):c.455T>A (p.Val152Asp)	ZNF419 (V120D +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486751	NM_024691.4(ZNF419):c.464C>T (p.Ser155Leu)	ZNF419 (S110L +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300536	NM_024691.4(ZNF419):c.494G>A (p.Gly165Glu)	ZNF419 (G119E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335710	NM_024691.4(ZNF419):c.584C>T (p.Ala195Val)	ZNF419 (A149V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195645	NM_024691.4(ZNF419):c.674A>G (p.His225Arg)	ZNF419 (H180R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784883	NM_024691.4(ZNF419):c.696A>G (p.Glu232=)	ZNF419	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2365959	NM_024691.4(ZNF419):c.725A>G (p.Asp242Gly)	ZNF419 (D210G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276498	NM_024691.4(ZNF419):c.726T>G (p.Asp242Glu)	ZNF419 (D209E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195646	NM_024691.4(ZNF419):c.787A>G (p.Asn263Asp)	ZNF419 (N230D +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2358464	NM_024691.4(ZNF419):c.808C>T (p.Arg270Cys)	ZNF419 (R238C +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195647	NM_024691.4(ZNF419):c.856C>G (p.Pro286Ala)	ZNF419 (P198A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393476	NM_024691.4(ZNF419):c.880A>G (p.Lys294Glu)	ZNF419 (K281E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489301	NM_024691.4(ZNF419):c.908T>C (p.Val303Ala)	ZNF419 (V304A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392202	NM_024691.4(ZNF419):c.911A>G (p.Gln304Arg)	ZNF419 (Q258R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195648	NM_024691.4(ZNF419):c.940C>A (p.Pro314Thr)	ZNF419 (P268T +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278056	NM_024691.4(ZNF419):c.991A>G (p.Met331Val)	ZNF419 (M285V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610783	NM_024691.4(ZNF419):c.998A>G (p.His333Arg)	ZNF419 (H334R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 769059	NM_024691.4(ZNF419):c.1006A>G (p.Ile336Val)	ZNF419 (I304V +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2239494	NM_024691.4(ZNF419):c.1025C>A (p.Pro342His)	ZNF419 (P254H +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335708	NM_024691.4(ZNF419):c.1105A>G (p.Arg369Gly)	ZNF419 (R281G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195641	NM_024691.4(ZNF419):c.1114A>G (p.Lys372Glu)	ZNF419 (K327E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2376302	NM_024691.4(ZNF419):c.1123G>A (p.Asp375Asn)	ZNF419 (D330N +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241959	NM_024691.4(ZNF419):c.1178A>G (p.His393Arg)	ZNF419 (H361R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456524	NM_024691.4(ZNF419):c.1199A>C (p.Lys400Thr)	ZNF419 (K312T +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329370	NM_024691.4(ZNF419):c.1220T>A (p.Phe407Tyr)	ZNF419 (F362Y +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598270	NM_024691.4(ZNF419):c.1285T>C (p.Cys429Arg)	ZNF419 (C417R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195642	NM_024691.4(ZNF419):c.1462T>C (p.Cys488Arg)	ZNF419 (C400R +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370135	NM_024691.4(ZNF419):c.1478G>A (p.Arg493His)	ZNF419 (R405H +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 685397	GRCh37/hg19 19q13.43(chr19:57952073-58661581)x3	C19orf18, VN1R1 +29 more	Copy number gain	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 564595	GRCh37/hg19 19q13.43(chr19:57891243-58536930)x3	ZNF814, ZSCAN4 +27 more	Copy number gain	not provided	GLikely benign
Select item 564590	GRCh37/hg19 19q13.43(chr19:57718739-58058739)x1	VN1R1, AURKC +14 more	Copy number loss	not provided	GUncertain significance
Select item 560059	Single allele	VN1R1, ZIK1 +12 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 394524	GRCh37/hg19 19q13.43(chr19:57988849-58015974)x3	ZNF419, ZNF772 +1 more	Copy number gain	See cases	Gconflicting data from submitters
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: 61