ClinVar Miner

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

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Total variants: 64
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HGVS dbSNP
NM_001127464.2(ZNF469):c.7554del (p.Ser2519Alafs) rs886039575
NM_001367624.1(ZNF469):c.10326G>C (p.Arg3442Ser) rs56236932
NM_001367624.1(ZNF469):c.10361G>A (p.Arg3454Gln) rs75288466
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.1069T>C (p.Ser357Pro) rs11648572
NM_001367624.1(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834
NM_001367624.1(ZNF469):c.10795G>T (p.Ala3599Ser) rs199760004
NM_001367624.1(ZNF469):c.1088C>T (p.Ser363Leu) rs771000169
NM_001367624.1(ZNF469):c.10975G>A (p.Gly3659Arg) rs3812951
NM_001367624.1(ZNF469):c.1098A>C (p.Arg366Ser) rs11640794
NM_001367624.1(ZNF469):c.10990= (p.Ala3664=) rs904783
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.1143C>A (p.Pro381=) rs74032864
NM_001367624.1(ZNF469):c.11496_11505del (p.Ser3833fs) rs1567517877
NM_001367624.1(ZNF469):c.11771C>T (p.Thr3924Met) rs139259830
NM_001367624.1(ZNF469):c.1285G>A (p.Ala429Thr) rs113937803
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.1697C>T (p.Ala566Val) rs181785233
NM_001367624.1(ZNF469):c.1827G>A (p.Ser609=) rs148616993
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.2814G>A (p.Ala938=) rs140480823
NM_001367624.1(ZNF469):c.2841G>A (p.Arg947=) rs150435442
NM_001367624.1(ZNF469):c.3153T>C (p.Ile1051=) rs9924504
NM_001367624.1(ZNF469):c.3516T>C (p.Arg1172=) rs111557381
NM_001367624.1(ZNF469):c.3522G>A (p.Pro1174=) rs9938800
NM_001367624.1(ZNF469):c.3568A>G (p.Lys1190Glu) rs7197071
NM_001367624.1(ZNF469):c.4343C>T (p.Pro1448Leu) rs4782300
NM_001367624.1(ZNF469):c.4419T>G (p.Ser1473=) rs12445417
NM_001367624.1(ZNF469):c.4421C>T (p.Ala1474Val) rs199897247
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.6444del (p.Gln2149fs) rs886044697
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.7675A>G (p.Lys2559Glu) rs146789160
NM_001367624.1(ZNF469):c.7981G>A (p.Gly2661Ser) rs138259179
NM_001367624.1(ZNF469):c.8076G>A (p.Pro2692=) rs149200506
NM_001367624.1(ZNF469):c.8093T>A (p.Leu2698Gln) rs3812956
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.8604C>T (p.Arg2868=) rs3812953
NM_001367624.1(ZNF469):c.8627A>G (p.His2876Arg) rs1983014
NM_001367624.1(ZNF469):c.8788G>T (p.Asp2930Tyr) rs76792613
NM_001367624.1(ZNF469):c.9125G>A (p.Arg3042His) rs150598363
NM_001367624.1(ZNF469):c.9131C>T (p.Thr3044Met) rs273585626
NM_001367624.1(ZNF469):c.9268C>T (p.Arg3090Ter) rs764139968
NM_001367624.1(ZNF469):c.946G>A (p.Glu316Lys) rs368772806
NM_001367624.1(ZNF469):c.9516C>T (p.Ala3172=) rs577913880
NM_001367624.1(ZNF469):c.9663C>T (p.Ser3221=) rs1555520265

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