ClinVar Miner

List of variants in gene ZNF423 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001379286.1(ZNF423):c.1655G>T (p.Gly552Val) rs34425379 0.00158
NM_001379286.1(ZNF423):c.807C>T (p.Asp269=) rs145503941 0.00101
NM_001379286.1(ZNF423):c.819C>T (p.Cys273=) rs201499268 0.00084
NM_001379286.1(ZNF423):c.1168T>C (p.Ser390Pro) rs142835239 0.00063
NM_001379286.1(ZNF423):c.2312C>T (p.Ala771Val) rs150234048 0.00041
NM_001379286.1(ZNF423):c.2400C>T (p.Thr800=) rs151102991 0.00035
NM_001379286.1(ZNF423):c.1132G>A (p.Ala378Thr) rs199760788 0.00011
NM_001379286.1(ZNF423):c.2649C>T (p.Ser883=) rs781131703 0.00008
NM_001379286.1(ZNF423):c.1176G>A (p.Pro392=) rs748728165 0.00005
NM_001379286.1(ZNF423):c.3245G>A (p.Arg1082His) rs370797524 0.00004
NM_001379286.1(ZNF423):c.166G>A (p.Val56Met) rs772307020 0.00003
NM_001379286.1(ZNF423):c.2846C>T (p.Ser949Leu) rs778403528 0.00002
NM_001379286.1(ZNF423):c.410A>T (p.Glu137Val) rs886043664 0.00001
NM_001379286.1(ZNF423):c.2933C>T (p.Ser978Leu) rs794727731
NM_001379286.1(ZNF423):c.3556G>A (p.Glu1186Lys) rs771530800

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