ClinVar Miner

List of variants in gene ZNF142 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_001379659.1(ZNF142):c.1556G>A (p.Arg519His) rs146514201 0.00531
NM_001379659.1(ZNF142):c.1284G>A (p.Ala428=) rs61733647 0.00476
NM_001379659.1(ZNF142):c.5116C>T (p.Arg1706Trp) rs72962069 0.00200
NM_001379659.1(ZNF142):c.2554T>G (p.Leu852Val) rs143333715 0.00143
NM_001379659.1(ZNF142):c.945G>A (p.Gln315=) rs186337382 0.00077
NM_001379659.1(ZNF142):c.1287G>T (p.Val429=)
NM_001379659.1(ZNF142):c.1590C>T (p.Ala530=)
NM_001379659.1(ZNF142):c.1848C>T (p.Leu616=) rs2106242230
NM_001379659.1(ZNF142):c.1874-4_1874-3del
NM_001379659.1(ZNF142):c.210A>G (p.Pro70=)
NM_001379659.1(ZNF142):c.2220G>A (p.Pro740=)
NM_001379659.1(ZNF142):c.2286T>C (p.His762=)
NM_001379659.1(ZNF142):c.2526C>T (p.His842=)
NM_001379659.1(ZNF142):c.2784G>A (p.Leu928=)
NM_001379659.1(ZNF142):c.3105C>T (p.Ala1035=)
NM_001379659.1(ZNF142):c.336C>T (p.Phe112=)
NM_001379659.1(ZNF142):c.3573A>T (p.Ser1191=)
NM_001379659.1(ZNF142):c.3579G>A (p.Thr1193=)
NM_001379659.1(ZNF142):c.3762C>T (p.Gly1254=)
NM_001379659.1(ZNF142):c.3837G>A (p.Pro1279=)
NM_001379659.1(ZNF142):c.4188G>C (p.Gly1396=)
NM_001379659.1(ZNF142):c.4191G>A (p.Val1397=)
NM_001379659.1(ZNF142):c.4308G>A (p.Thr1436=)
NM_001379659.1(ZNF142):c.43G>A (p.Gly15Arg)
NM_001379659.1(ZNF142):c.4962C>T (p.Cys1654=)
NM_001379659.1(ZNF142):c.504G>T (p.Val168=)
NM_001379659.1(ZNF142):c.510A>G (p.Arg170=)
NM_001379659.1(ZNF142):c.5398C>T (p.Arg1800Cys)
NM_001379659.1(ZNF142):c.5448C>T (p.Thr1816=)
NM_001379659.1(ZNF142):c.702C>T (p.Phe234=)

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