ClinVar Miner

List of variants in gene ZNF469 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_001367624.2(ZNF469):c.1489G>A (p.Gly497Arg) rs28723506 0.09509
NM_001367624.2(ZNF469):c.6470G>A (p.Arg2157Lys) rs13334190 0.09442
NM_001367624.2(ZNF469):c.1697C>T (p.Ala566Val) rs181785233 0.00939
NM_001367624.2(ZNF469):c.7079C>T (p.Pro2360Leu) rs76389306 0.00188
NM_001367624.2(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834 0.00185
NM_001367624.2(ZNF469):c.5644G>A (p.Ala1882Thr) rs74032866 0.00185
NM_001367624.2(ZNF469):c.946G>A (p.Glu316Lys) rs368772806 0.00085
NM_001367624.2(ZNF469):c.11425G>A (p.Glu3809Lys) rs201834513 0.00081
NM_001367624.2(ZNF469):c.2035G>A (p.Glu679Lys) rs551591362 0.00080
NM_001367624.2(ZNF469):c.19C>T (p.Arg7Ter) rs1004428835 0.00037
NM_001367624.2(ZNF469):c.8996G>T (p.Gly2999Val) rs273585625 0.00034
NM_001367624.2(ZNF469):c.845G>A (p.Gly282Glu) rs757999676 0.00029
NM_001367624.2(ZNF469):c.9214G>A (p.Gly3072Ser) rs557364171 0.00019
NM_001367624.2(ZNF469):c.10889G>A (p.Arg3630His) rs758123475 0.00013
NM_001367624.2(ZNF469):c.6809C>A (p.Ser2270Tyr) rs273585624 0.00010
NM_001367624.2(ZNF469):c.8426C>T (p.Pro2809Leu) rs1054270904 0.00009
NM_001367624.2(ZNF469):c.992C>T (p.Ala331Val) rs149485731 0.00006
NM_001367624.2(ZNF469):c.6880G>A (p.Gly2294Arg) rs773187176 0.00005
NM_001367624.2(ZNF469):c.9050G>A (p.Ser3017Asn) rs1383712865 0.00005
NM_001367624.2(ZNF469):c.10324del (p.Arg3442fs) rs756543273 0.00004
NM_001367624.2(ZNF469):c.2063C>A (p.Thr688Asn) rs281865146 0.00004
NM_001367624.2(ZNF469):c.290C>T (p.Pro97Leu) rs273585617 0.00004
NM_001367624.2(ZNF469):c.4276G>A (p.Glu1426Lys) rs868174994 0.00004
NM_001367624.2(ZNF469):c.3119A>C (p.Lys1040Thr) rs273585619 0.00002
NM_001367624.2(ZNF469):c.99G>A (p.Pro33=) rs273585631 0.00002
NM_001367624.2(ZNF469):c.10707C>A (p.Cys3569Ter) rs760186083 0.00001
NM_001367624.2(ZNF469):c.4271C>A (p.Ser1424Tyr) rs1022664528 0.00001
NM_001367624.2(ZNF469):c.5384C>A (p.Ala1795Asp) rs1013562167 0.00001
NM_001367624.2(ZNF469):c.6073G>C (p.Ala2025Pro) rs1318556892 0.00001
NM_001367624.2(ZNF469):c.9131C>T (p.Thr3044Met) rs273585626 0.00001
NM_001367624.2(ZNF469):c.10325G>C (p.Arg3442Thr) rs199528724
NM_001367624.2(ZNF469):c.10332del (p.Arg3445fs) rs764470052
NM_001367624.2(ZNF469):c.10794G>A (p.Gly3598=)
NM_001367624.2(ZNF469):c.11536dup (p.Arg3846fs) rs1192814702
NM_001367624.2(ZNF469):c.11671C>G (p.Leu3891Val) rs1419259989
NM_001367624.2(ZNF469):c.1534G>A (p.Glu512Lys) rs953454298
NM_001367624.2(ZNF469):c.2059G>A (p.Glu687Lys)
NM_001367624.2(ZNF469):c.2130_2132delinsCCG (p.Pro711Arg)
NM_001367624.2(ZNF469):c.2477C>G (p.Pro826Arg) rs772056680
NM_001367624.2(ZNF469):c.2898GTCGGG[1] (p.967SG[1]) rs281865147
NM_001367624.2(ZNF469):c.3003C>T (p.Ala1001=) rs993032767
NM_001367624.2(ZNF469):c.4112dup (p.Pro1373fs)
NM_001367624.2(ZNF469):c.4516G>A (p.Glu1506Lys) rs2142306246
NM_001367624.2(ZNF469):c.5402del (p.Val1801fs)
NM_001367624.2(ZNF469):c.5613_5622del (p.Arg1871fs)
NM_001367624.2(ZNF469):c.7874_7877dup (p.His2626fs)
NM_001367624.2(ZNF469):c.8035C>T (p.Leu2679Phe) rs1304525923
NM_001367624.2(ZNF469):c.8350C>T (p.Arg2784Ter) rs1172315984
NM_001367624.2(ZNF469):c.8428del (p.Ala2810fs) rs2142312393
NM_001367624.2(ZNF469):c.9268C>T (p.Arg3090Ter) rs764139968

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