ClinVar Miner

List of variants in gene ZNF469 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 34
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HGVS dbSNP
NM_001367624.1(ZNF469):c.10582G>A (p.Glu3528Lys) rs758708056
NM_001367624.1(ZNF469):c.10683C>T (p.Ala3561=) rs794727258
NM_001367624.1(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834
NM_001367624.1(ZNF469):c.1088C>T (p.Ser363Leu) rs771000169
NM_001367624.1(ZNF469):c.11277C>T (p.Ser3759=) rs372634401
NM_001367624.1(ZNF469):c.11278G>A (p.Glu3760Lys) rs547014159
NM_001367624.1(ZNF469):c.11771C>T (p.Thr3924Met) rs139259830
NM_001367624.1(ZNF469):c.1483C>T (p.Pro495Ser) rs202205643
NM_001367624.1(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001367624.1(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001367624.1(ZNF469):c.2017G>A (p.Ala673Thr) rs770623245
NM_001367624.1(ZNF469):c.2270T>G (p.Leu757Arg) rs753664726
NM_001367624.1(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145
NM_001367624.1(ZNF469):c.248C>T (p.Pro83Leu) rs775103017
NM_001367624.1(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481
NM_001367624.1(ZNF469):c.2841G>A (p.Arg947=) rs150435442
NM_001367624.1(ZNF469):c.4422G>A (p.Ala1474=) rs368877287
NM_001367624.1(ZNF469):c.4427G>A (p.Arg1476Lys) rs763632522
NM_001367624.1(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076
NM_001367624.1(ZNF469):c.4556C>T (p.Ser1519Leu) rs767278971
NM_001367624.1(ZNF469):c.457C>G (p.Pro153Ala) rs532620482
NM_001367624.1(ZNF469):c.4829G>A (p.Arg1610His) rs567038987
NM_001367624.1(ZNF469):c.4952A>G (p.Gln1651Arg) rs773925755
NM_001367624.1(ZNF469):c.5340C>G (p.Pro1780=) rs184374078
NM_001367624.1(ZNF469):c.725_726delinsTT (p.Ser242Ile) rs886043704
NM_001367624.1(ZNF469):c.7267C>A (p.Pro2423Thr) rs199727372
NM_001367624.1(ZNF469):c.7981G>A (p.Gly2661Ser) rs138259179
NM_001367624.1(ZNF469):c.8425C>G (p.Pro2809Ala) rs794727257
NM_001367624.1(ZNF469):c.8477A>G (p.Asp2826Gly) rs886043475
NM_001367624.1(ZNF469):c.8489G>C (p.Gly2830Ala) rs541325052
NM_001367624.1(ZNF469):c.8788G>T (p.Asp2930Tyr) rs76792613
NM_001367624.1(ZNF469):c.9131C>T (p.Thr3044Met) rs273585626
NM_001367624.1(ZNF469):c.9516C>T (p.Ala3172=) rs577913880
NM_001367624.1(ZNF469):c.9663C>T (p.Ser3221=) rs1555520265

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