ClinVar Miner

List of variants in gene ZNF469 reported as uncertain significance for not specified

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001367624.2(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076 0.00255
NM_001367624.2(ZNF469):c.10330G>C (p.Gly3444Arg) rs569602115 0.00135
NM_001367624.2(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145 0.00111
NM_001367624.2(ZNF469):c.11425G>A (p.Glu3809Lys) rs201834513 0.00081
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.4855G>A (p.Glu1619Lys) rs759327672 0.00026
NM_001367624.2(ZNF469):c.5914G>A (p.Gly1972Arg) rs766410344 0.00019
NM_001367624.2(ZNF469):c.9214G>A (p.Gly3072Ser) rs557364171 0.00019
NM_001367624.2(ZNF469):c.7523C>T (p.Ala2508Val) rs570690992 0.00018
NM_001367624.2(ZNF469):c.334G>A (p.Ala112Thr) rs766853024 0.00016
NM_001367624.2(ZNF469):c.10889G>A (p.Arg3630His) rs758123475 0.00013
NM_001367624.2(ZNF469):c.11107G>A (p.Val3703Met) rs151127652 0.00013
NM_001367624.2(ZNF469):c.5266G>A (p.Ala1756Thr) rs371328036 0.00012
NM_001367624.2(ZNF469):c.6809C>A (p.Ser2270Tyr) rs273585624 0.00010
NM_001367624.2(ZNF469):c.3452C>T (p.Ala1151Val) rs755348435 0.00009
NM_001367624.2(ZNF469):c.4001C>T (p.Pro1334Leu) rs1016116935 0.00009
NM_001367624.2(ZNF469):c.80C>T (p.Pro27Leu) rs1009769670 0.00009
NM_001367624.2(ZNF469):c.8426C>T (p.Pro2809Leu) rs1054270904 0.00009
NM_001367624.2(ZNF469):c.11221G>A (p.Gly3741Ser) rs745385522 0.00006
NM_001367624.2(ZNF469):c.1663G>A (p.Asp555Asn) rs749179728 0.00006
NM_001367624.2(ZNF469):c.749T>A (p.Val250Asp) rs764273631 0.00006
NM_001367624.2(ZNF469):c.7574C>T (p.Pro2525Leu) rs756003807 0.00006
NM_001367624.2(ZNF469):c.992C>T (p.Ala331Val) rs149485731 0.00006
NM_001367624.2(ZNF469):c.186G>T (p.Glu62Asp) rs770775791 0.00005
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.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.536G>C (p.Gly179Ala) rs760014906 0.00004
NM_001367624.2(ZNF469):c.10184A>G (p.Glu3395Gly) rs900191925 0.00003
NM_001367624.2(ZNF469):c.10984C>T (p.Arg3662Ter) rs1171824548 0.00003
NM_001367624.2(ZNF469):c.11444C>T (p.Thr3815Met) rs1057518368 0.00003
NM_001367624.2(ZNF469):c.3550G>A (p.Ala1184Thr) rs553460850 0.00003
NM_001367624.2(ZNF469):c.4609G>A (p.Gly1537Ser) rs528560466 0.00003
NM_001367624.2(ZNF469):c.523G>A (p.Ala175Thr) rs1085307628 0.00003
NM_001367624.2(ZNF469):c.8438C>G (p.Thr2813Ser) rs985304000 0.00003
NM_001367624.2(ZNF469):c.8762G>A (p.Cys2921Tyr) rs1029645463 0.00003
NM_001367624.2(ZNF469):c.1543G>A (p.Gly515Arg) rs1131691990 0.00002
NM_001367624.2(ZNF469):c.3119A>C (p.Lys1040Thr) rs273585619 0.00002
NM_001367624.2(ZNF469):c.1072C>T (p.Pro358Ser) rs1064796784 0.00001
NM_001367624.2(ZNF469):c.10811C>T (p.Pro3604Leu) rs957402222 0.00001
NM_001367624.2(ZNF469):c.11344G>A (p.Ala3782Thr) rs1327878609 0.00001
NM_001367624.2(ZNF469):c.2126C>T (p.Pro709Leu) rs1017679214 0.00001
NM_001367624.2(ZNF469):c.2308C>T (p.Pro770Ser) rs1039078920 0.00001
NM_001367624.2(ZNF469):c.2309C>T (p.Pro770Leu) rs1425767356 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.578C>A (p.Ser193Tyr) rs1369047197 0.00001
NM_001367624.2(ZNF469):c.6073G>C (p.Ala2025Pro) rs1318556892 0.00001
NM_001367624.2(ZNF469):c.8984C>T (p.Ala2995Val) rs759398721 0.00001
NM_001367624.2(ZNF469):c.9131C>T (p.Thr3044Met) rs273585626 0.00001
NM_001367624.2(ZNF469):c.9335G>A (p.Arg3112Gln) rs942909542 0.00001
NM_001367624.2(ZNF469):c.9448G>A (p.Glu3150Lys) rs777096338 0.00001
NM_001367624.2(ZNF469):c.9622C>T (p.Arg3208Trp) rs936945500 0.00001
NM_001127464.2(ZNF469):c.5576_5577delCCinsAG (p.Thr1859Lys) rs1555519640
NM_001367624.2(ZNF469):c.10199C>T (p.Pro3400Leu) rs281165933
NM_001367624.2(ZNF469):c.10294C>T (p.Gln3432Ter) rs1085307609
NM_001367624.2(ZNF469):c.10325G>A (p.Arg3442Lys) rs199528724
NM_001367624.2(ZNF469):c.11536dup (p.Arg3846fs) rs1192814702
NM_001367624.2(ZNF469):c.11671C>G (p.Leu3891Val) rs1419259989
NM_001367624.2(ZNF469):c.11714C>G (p.Pro3905Arg) rs529322092
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.2789G>T (p.Gly930Val) rs564654481
NM_001367624.2(ZNF469):c.2898GTCGGG[1] (p.967SG[1]) rs281865147
NM_001367624.2(ZNF469):c.3079C>A (p.Arg1027Ser) rs1057524853
NM_001367624.2(ZNF469):c.4516G>A (p.Glu1506Lys) rs2142306246
NM_001367624.2(ZNF469):c.5158G>A (p.Val1720Ile) rs1131691303
NM_001367624.2(ZNF469):c.7628G>A (p.Arg2543Gln) rs771550262
NM_001367624.2(ZNF469):c.8035C>T (p.Leu2679Phe) rs1304525923
NM_001367624.2(ZNF469):c.9245C>T (p.Ala3082Val) rs1015869921
NM_001367624.2(ZNF469):c.9368G>A (p.Arg3123His) rs536601676

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