ClinVar Miner

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

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Total variants: 25
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HGVS dbSNP
NM_001127464.2(ZNF469):c.10242G>C (p.Arg3414Ser) rs56236932
NM_001127464.2(ZNF469):c.1069T>C (p.Ser357Pro) rs11648572
NM_001127464.2(ZNF469):c.10711G>T (p.Ala3571Ser) rs199760004
NM_001127464.2(ZNF469):c.10891G>A (p.Gly3631Arg) rs3812951
NM_001127464.2(ZNF469):c.10906G= (p.Ala3636=) rs904783
NM_001127464.2(ZNF469):c.1098A>C (p.Arg366Ser) rs11640794
NM_001127464.2(ZNF469):c.1143C>A (p.Pro381=) rs74032864
NM_001127464.2(ZNF469):c.1285G>A (p.Ala429Thr) rs113937803
NM_001127464.2(ZNF469):c.1697C>T (p.Ala566Val) rs181785233
NM_001127464.2(ZNF469):c.1827G>A (p.Ser609=) rs148616993
NM_001127464.2(ZNF469):c.2814G>A (p.Ala938=) rs140480823
NM_001127464.2(ZNF469):c.3153T>C (p.Ile1051=) rs9924504
NM_001127464.2(ZNF469):c.3432T>C (p.Arg1144=) rs111557381
NM_001127464.2(ZNF469):c.3438G>A (p.Pro1146=) rs9938800
NM_001127464.2(ZNF469):c.3484A>G (p.Lys1162Glu) rs7197071
NM_001127464.2(ZNF469):c.4259C>T (p.Pro1420Leu) rs4782300
NM_001127464.2(ZNF469):c.4335T>G (p.Ser1445=) rs12445417
NM_001127464.2(ZNF469):c.4337C>T (p.Ala1446Val) rs199897247
NM_001127464.2(ZNF469):c.7591A>G (p.Lys2531Glu) rs146789160
NM_001127464.2(ZNF469):c.7992G>A (p.Pro2664=) rs149200506
NM_001127464.2(ZNF469):c.8009T>A (p.Leu2670Gln) rs3812956
NM_001127464.2(ZNF469):c.8520C>T (p.Arg2840=) rs3812953
NM_001127464.2(ZNF469):c.8543A>G (p.His2848Arg) rs1983014
NM_001127464.2(ZNF469):c.9041G>A (p.Arg3014His) rs150598363
NM_001127464.2(ZNF469):c.946G>A (p.Glu316Lys) rs368772806

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