ClinVar Miner

List of variants in gene ZNF469 reported as likely benign for not provided

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Total variants: 22
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HGVS dbSNP
NM_001127464.2(ZNF469):c.10434G>A (p.Pro3478=) rs376379111
NM_001127464.2(ZNF469):c.10572G>A (p.Pro3524=) rs191234581
NM_001127464.2(ZNF469):c.10616G>A (p.Gly3539Glu) rs199610834
NM_001127464.2(ZNF469):c.10711G>T (p.Ala3571Ser) rs199760004
NM_001127464.2(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001127464.2(ZNF469):c.2666C>T (p.Ala889Val) rs145186655
NM_001127464.2(ZNF469):c.3257G>T (p.Arg1086Leu) rs568046708
NM_001127464.2(ZNF469):c.3689C>A (p.Ala1230Glu) rs141255631
NM_001127464.2(ZNF469):c.3866A>G (p.Lys1289Arg) rs772817384
NM_001127464.2(ZNF469):c.4279C>G (p.Leu1427Val) rs116532825
NM_001127464.2(ZNF469):c.4388C>T (p.Thr1463Met) rs375045076
NM_001127464.2(ZNF469):c.4694C>T (p.Ser1565Leu) rs768864900
NM_001127464.2(ZNF469):c.498C>G (p.Leu166=) rs1555518472
NM_001127464.2(ZNF469):c.5003C>T (p.Pro1668Leu) rs115487796
NM_001127464.2(ZNF469):c.5464C>A (p.Pro1822Thr) rs199932922
NM_001127464.2(ZNF469):c.6249C>T (p.Ala2083=) rs1039243677
NM_001127464.2(ZNF469):c.6515C>T (p.Thr2172Ile) rs1465493306
NM_001127464.2(ZNF469):c.7591A>G (p.Lys2531Glu) rs146789160
NM_001127464.2(ZNF469):c.9011_9025delTTCCCGGGAACACCC (p.Leu3004_Thr3008del) rs281865162
NM_001127464.2(ZNF469):c.9589G>A (p.Ala3197Thr) rs1046436333
NM_001127464.2(ZNF469):c.9612G>A (p.Thr3204=) rs573582117
NM_001367624.1(ZNF469):c.9018C>T (p.Ala3006=)

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