ZNF429[gene] - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 59114	GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	ABHD8, ADGRE2 +695 more	Copy number gain	See cases	GPathogenic
Select item 147522	GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3	ABHD8, AKAP8 +574 more	Copy number gain	See cases	GPathogenic
Select item 57042	GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	LOC130064154, LOC130064155 +625 more	Copy number gain	See cases	GPathogenic
Select item 153725	GRCh38/hg38 19p12(chr19:20637987-21976216)x3	LINC00664, LOC105372321 +27 more	Copy number gain	See cases	GUncertain significance
Select item 3195695	NM_001001415.4(ZNF429):c.59G>A (p.Cys20Tyr)	ZNF429 (C18Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2303962	NM_001001415.4(ZNF429):c.122T>C (p.Val41Ala)	ZNF429 (V41A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335738	NM_001001415.4(ZNF429):c.185C>G (p.Pro62Arg)	ZNF429 (P30R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303764	NM_001001415.4(ZNF429):c.185C>A (p.Pro62His)	ZNF429 (P60H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335741	NM_001001415.4(ZNF429):c.291A>C (p.Lys97Asn)	ZNF429 (K95N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195693	NM_001001415.4(ZNF429):c.307T>C (p.Tyr103His)	ZNF429 (Y101H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491401	NM_001001415.4(ZNF429):c.316C>T (p.Arg106Cys)	ZNF429 (R106C +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537128	NM_001001415.4(ZNF429):c.376T>C (p.Tyr126His)	ZNF429 (Y124H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195694	NM_001001415.4(ZNF429):c.377A>G (p.Tyr126Cys)	ZNF429 (Y124C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525947	NM_001001415.4(ZNF429):c.434A>G (p.Tyr145Cys)	ZNF429 (Y81C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611260	NM_001001415.4(ZNF429):c.478G>A (p.Ala160Thr)	ZNF429 (A128T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369850	NM_001001415.4(ZNF429):c.493A>G (p.Thr165Ala)	ZNF429 (T101A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521397	NM_001001415.4(ZNF429):c.503C>T (p.Thr168Ile)	ZNF429 (T168I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326675	NM_001001415.4(ZNF429):c.650C>A (p.Thr217Asn)	ZNF429 (T153N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327568	NM_001001415.4(ZNF429):c.662G>C (p.Arg221Thr)	ZNF429 (R189T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195696	NM_001001415.4(ZNF429):c.739C>T (p.His247Tyr)	ZNF429 (H245Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2921055	NM_001001415.4(ZNF429):c.952del (p.Cys318fs)	ZNF429 (C286fs +3 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2213661	NM_001001415.4(ZNF429):c.971G>A (p.Arg324Gln)	ZNF429 (R324Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292520	NM_001001415.4(ZNF429):c.1004A>C (p.His335Pro)	ZNF429 (H303P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195686	NM_001001415.4(ZNF429):c.1033G>A (p.Glu345Lys)	ZNF429 (E313K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195687	NM_001001415.4(ZNF429):c.1054T>C (p.Trp352Arg)	ZNF429 (W320R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355259	NM_001001415.4(ZNF429):c.1106A>G (p.Tyr369Cys)	ZNF429 (Y305C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195688	NM_001001415.4(ZNF429):c.1115A>G (p.Glu372Gly)	ZNF429 (E308G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203957	NM_001001415.4(ZNF429):c.1160A>G (p.His387Arg)	ZNF429 (H323R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335742	NM_001001415.4(ZNF429):c.1178G>T (p.Gly393Val)	ZNF429 (G391V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335739	NM_001001415.4(ZNF429):c.1193A>C (p.Lys398Thr)	ZNF429 (K334T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554135	NM_001001415.4(ZNF429):c.1303A>G (p.Thr435Ala)	ZNF429 (T435A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217116	NM_001001415.4(ZNF429):c.1340A>G (p.His447Arg)	ZNF429 (H447R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522212	NM_001001415.4(ZNF429):c.1391G>A (p.Arg464Gln)	ZNF429 (R462Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266863	NM_001001415.4(ZNF429):c.1486C>T (p.Leu496Phe)	ZNF429 (L432F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195689	NM_001001415.4(ZNF429):c.1506T>G (p.Ile502Met)	ZNF429 (I438M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364522	NM_001001415.4(ZNF429):c.1643G>A (p.Arg548Gln)	ZNF429 (R548Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195690	NM_001001415.4(ZNF429):c.1691C>T (p.Pro564Leu)	ZNF429 (P500L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230496	NM_001001415.4(ZNF429):c.1726C>T (p.His576Tyr)	ZNF429 (H544Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195691	NM_001001415.4(ZNF429):c.1727A>C (p.His576Pro)	ZNF429 (H512P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388958	NM_001001415.4(ZNF429):c.1800A>C (p.Lys600Asn)	ZNF429 (K600N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554136	NM_001001415.4(ZNF429):c.1892C>A (p.Thr631Asn)	ZNF429 (T567N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195692	NM_001001415.4(ZNF429):c.1894C>T (p.Arg632Trp)	ZNF429 (R600W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222143	NM_001001415.4(ZNF429):c.1942G>C (p.Val648Leu)	ZNF429 (V584L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335743	NM_001001415.4(ZNF429):c.1952C>A (p.Ala651Asp)	ZNF429 (A587D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404709	NM_001001415.4(ZNF429):c.1960C>T (p.Pro654Ser)	ZNF429 (P590S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649623	NM_001001415.4(ZNF429):c.1978A>C (p.Arg660=)	ZNF429	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2405432	NM_001001415.4(ZNF429):c.1982G>A (p.Gly661Asp)	ZNF429 (G597D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649624	NM_001001415.4(ZNF429):c.1983T>C (p.Gly661=)	ZNF429	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2395689	NM_001001415.4(ZNF429):c.1987C>T (p.Arg663Trp)	ZNF429 (R631W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649625	NC_000019.10:g.21541807G>A	ZNF429	Single nucleotide variant	not provided	GLikely benign
Select item 2649626	NC_000019.10:g.21541813T>G	ZNF429	Single nucleotide variant	not provided	GLikely benign
Select item 1330177	GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	ACP7, ACTMAP +255 more	Copy number gain	Specific learning disability	GPathogenic
Select item 816071	GRCh37/hg19 19p12(chr19:21717186-23008275)x3	ZNF100, ZNF208 +8 more	Copy number gain	not provided	GLikely benign
Select item 816070	GRCh37/hg19 19p12(chr19:21683086-21777328)x1	ZNF429	Copy number loss	not provided	GUncertain significance
Select item 564603	GRCh37/hg19 19p13.11-12(chr19:19903805-21966609)x1	ZNF737, ZNF708 +14 more	Copy number loss	not provided	GUncertain significance
Select item 564592	GRCh37/hg19 19p12(chr19:21544570-21986301)x3	ZNF429, ZNF493 +1 more	Copy number gain	not provided	GLikely benign
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 221350	chr19:19230868-24115369 complex variant	ATP13A1, BORCS8 +49 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 60