ClinVar Miner

List of variants in gene ZNF469 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_001367624.2(ZNF469):c.1471G>A (p.Ala491Thr) rs117555121 0.00632
NM_001367624.2(ZNF469):c.9919A>G (p.Thr3307Ala) rs273585627 0.00072
NM_001367624.2(ZNF469):c.11318G>A (p.Arg3773Gln) rs571622809 0.00056
NM_001367624.2(ZNF469):c.8344C>T (p.His2782Tyr) rs553227769 0.00051
NM_001367624.2(ZNF469):c.216G>T (p.Glu72Asp) rs543285355 0.00032
NM_001367624.2(ZNF469):c.6629T>C (p.Leu2210Pro) rs564413710 0.00029
NM_001367624.2(ZNF469):c.10717G>A (p.Gly3573Arg) rs183149417 0.00026
NM_001367624.2(ZNF469):c.1020C>T (p.Gly340=) rs273585633 0.00022
NM_001367624.2(ZNF469):c.1522G>A (p.Ala508Thr) rs750005577 0.00022
NM_001367624.2(ZNF469):c.5162G>T (p.Cys1721Phe) rs568197988 0.00021
NM_001367624.2(ZNF469):c.5915G>T (p.Gly1972Val) rs573931575 0.00021
NM_001367624.2(ZNF469):c.3931C>T (p.Pro1311Ser) rs187453092 0.00016
NM_001367624.2(ZNF469):c.11107G>A (p.Val3703Met) rs151127652 0.00013
NM_001367624.2(ZNF469):c.941C>T (p.Pro314Leu) rs777666112 0.00013
NM_001367624.2(ZNF469):c.10354G>A (p.Gly3452Ser) rs548646578 0.00012
NM_001367624.2(ZNF469):c.5266G>A (p.Ala1756Thr) rs371328036 0.00012
NM_001367624.2(ZNF469):c.11185G>A (p.Gly3729Ser) rs273585629 0.00009
NM_001367624.2(ZNF469):c.11545C>T (p.Arg3849Trp) rs770109867 0.00009
NM_001367624.2(ZNF469):c.1430C>T (p.Pro477Leu) rs1336355924 0.00008
NM_001367624.2(ZNF469):c.7195C>T (p.Pro2399Ser) rs759032227 0.00008
NM_001367624.2(ZNF469):c.8387C>G (p.Pro2796Arg) rs886052412 0.00008
NM_001367624.2(ZNF469):c.8931C>G (p.His2977Gln) rs758398877 0.00008
NM_001367624.2(ZNF469):c.3919G>A (p.Gly1307Ser) rs568553875 0.00007
NM_001367624.2(ZNF469):c.4829G>A (p.Arg1610His) rs567038987 0.00007
NM_001367624.2(ZNF469):c.4910G>A (p.Arg1637Gln) rs273585621 0.00006
NM_001367624.2(ZNF469):c.7090G>A (p.Ala2364Thr) rs957383204 0.00006
NM_001367624.2(ZNF469):c.7831G>A (p.Glu2611Lys) rs281865151 0.00006
NM_001367624.2(ZNF469):c.992C>T (p.Ala331Val) rs149485731 0.00006
NM_001367624.2(ZNF469):c.356G>A (p.Arg119His) rs759962057 0.00005
NM_001367624.2(ZNF469):c.5332C>A (p.Pro1778Thr) rs528985816 0.00005
NM_001367624.2(ZNF469):c.7645G>A (p.Val2549Ile) rs759325304 0.00005
NM_001367624.2(ZNF469):c.98C>T (p.Pro33Leu) rs752770883 0.00005
NM_001367624.2(ZNF469):c.10324del (p.Arg3442fs) rs756543273 0.00004
NM_001367624.2(ZNF469):c.11530C>T (p.Pro3844Ser) rs866162306 0.00004
NM_001367624.2(ZNF469):c.5967C>T (p.Ala1989=) rs955767732 0.00004
NM_001367624.2(ZNF469):c.8080C>T (p.Arg2694Cys) rs540443650 0.00004
NM_001367624.2(ZNF469):c.-2C>T rs1048563743 0.00003
NM_001367624.2(ZNF469):c.10480C>T (p.Arg3494Trp) rs921811959 0.00003
NM_001367624.2(ZNF469):c.11278G>A (p.Glu3760Lys) rs547014159 0.00003
NM_001367624.2(ZNF469):c.1418G>A (p.Arg473Gln) rs775578805 0.00003
NM_001367624.2(ZNF469):c.2123C>T (p.Ala708Val) rs1327795344 0.00003
NM_001367624.2(ZNF469):c.11567G>A (p.Arg3856His) rs187075195 0.00002
NM_001367624.2(ZNF469):c.1475G>A (p.Arg492Gln) rs919081661 0.00002
NM_001367624.2(ZNF469):c.7444C>T (p.Arg2482Cys) rs1002940022 0.00002
NM_001367624.2(ZNF469):c.10352G>A (p.Arg3451His) rs972190166 0.00001
NM_001367624.2(ZNF469):c.1339C>T (p.Pro447Ser) rs931930346 0.00001
NM_001367624.2(ZNF469):c.1346C>T (p.Pro449Leu) rs1388799029 0.00001
NM_001367624.2(ZNF469):c.1750G>A (p.Val584Met) rs1374471776 0.00001
NM_001367624.2(ZNF469):c.2332G>A (p.Ala778Thr) rs761152033 0.00001
NM_001367624.2(ZNF469):c.2695C>T (p.Pro899Ser) rs973845764 0.00001
NM_001367624.2(ZNF469):c.2953G>A (p.Gly985Ser) rs886052399 0.00001
NM_001367624.2(ZNF469):c.3055C>T (p.Pro1019Ser) rs937180195 0.00001
NM_001367624.2(ZNF469):c.3394G>A (p.Glu1132Lys) rs1310255108 0.00001
NM_001367624.2(ZNF469):c.5114C>T (p.Thr1705Ile) rs768667107 0.00001
NM_001367624.2(ZNF469):c.7298C>T (p.Thr2433Ile) rs1026835942 0.00001
NM_001367624.2(ZNF469):c.7595G>T (p.Arg2532Met) rs553909579 0.00001
NM_001367624.2(ZNF469):c.8908G>T (p.Gly2970Cys) rs1426809592 0.00001
NM_001367624.2(ZNF469):c.9055G>A (p.Glu3019Lys) rs765339766 0.00001
NM_001367624.2(ZNF469):c.9088G>A (p.Gly3030Ser) rs773580012 0.00001
NM_001367624.2(ZNF469):c.9977C>A (p.Thr3326Asn) rs1206417002 0.00001
NM_001367624.2(ZNF469):c.10328G>T (p.Gly3443Val) rs140056980
NM_001367624.2(ZNF469):c.11017C>T (p.Pro3673Ser) rs1275132253
NM_001367624.2(ZNF469):c.11632C>G (p.Arg3878Gly)
NM_001367624.2(ZNF469):c.11714_11715delinsAT (p.Pro3905His) rs2142318310
NM_001367624.2(ZNF469):c.1625G>A (p.Gly542Asp) rs2142299887
NM_001367624.2(ZNF469):c.1640T>C (p.Leu547Pro) rs1905926907
NM_001367624.2(ZNF469):c.2644G>A (p.Gly882Arg)
NM_001367624.2(ZNF469):c.362T>C (p.Ile121Thr) rs1555518437
NM_001367624.2(ZNF469):c.3759G>A (p.Ala1253=) rs543669472
NM_001367624.2(ZNF469):c.457C>A (p.Pro153Thr) rs532620482
NM_001367624.2(ZNF469):c.4731G>C (p.Arg1577Ser) rs1906243073
NM_001367624.2(ZNF469):c.5186C>T (p.Pro1729Leu)
NM_001367624.2(ZNF469):c.5618C>T (p.Ala1873Val)
NM_001367624.2(ZNF469):c.5706A>G (p.Ile1902Met) rs1597210698
NM_001367624.2(ZNF469):c.5798C>T (p.Pro1933Leu)
NM_001367624.2(ZNF469):c.7013G>A (p.Gly2338Asp) rs1597211750
NM_001367624.2(ZNF469):c.725_726delinsTT (p.Ser242Ile) rs886043704
NM_001367624.2(ZNF469):c.7838G>C (p.Arg2613Pro) rs370285147
NM_001367624.2(ZNF469):c.7931G>T (p.Arg2644Leu) rs281865152
NM_001367624.2(ZNF469):c.9234C>G (p.Phe3078Leu) rs576267702
NM_001367624.2(ZNF469):c.9245C>G (p.Ala3082Gly) rs1015869921
NM_001367624.2(ZNF469):c.9387G>C (p.Glu3129Asp) rs1906616801
NM_001367624.2(ZNF469):c.9730T>C (p.Ser3244Pro) rs1597213923

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