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: 87
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HGVS dbSNP
NM_001127464.2(ZNF469):c.4448_4450delTGC (p.Leu1483del) rs555544144
NM_001127464.2(ZNF469):c.5576_5577delCCinsAG (p.Thr1859Lys) rs1555519640
NM_001367624.1(ZNF469):c.10079G>T (p.Ser3360Ile) rs929128705
NM_001367624.1(ZNF469):c.10184A>G (p.Glu3395Gly) rs900191925
NM_001367624.1(ZNF469):c.10294C>T (p.Gln3432Ter) rs1085307609
NM_001367624.1(ZNF469):c.10325G>A (p.Arg3442Lys) rs199528724
NM_001367624.1(ZNF469):c.10328G>A (p.Gly3443Glu) rs140056980
NM_001367624.1(ZNF469):c.10330G>C (p.Gly3444Arg) rs569602115
NM_001367624.1(ZNF469):c.1072C>T (p.Pro358Ser) rs1064796784
NM_001367624.1(ZNF469):c.10762G>A (p.Gly3588Arg) rs750481489
NM_001367624.1(ZNF469):c.10888C>T (p.Arg3630Cys) rs200668806
NM_001367624.1(ZNF469):c.10984C>T (p.Arg3662Ter) rs1171824548
NM_001367624.1(ZNF469):c.11107G>A (p.Val3703Met) rs151127652
NM_001367624.1(ZNF469):c.11203A>G (p.Ser3735Gly) rs536054902
NM_001367624.1(ZNF469):c.11221G>A (p.Gly3741Ser) rs745385522
NM_001367624.1(ZNF469):c.11344G>A (p.Ala3782Thr) rs1327878609
NM_001367624.1(ZNF469):c.11425G>A (p.Glu3809Lys) rs201834513
NM_001367624.1(ZNF469):c.11444C>T (p.Thr3815Met) rs1057518368
NM_001367624.1(ZNF469):c.11697A>C (p.Arg3899Ser) rs561879014
NM_001367624.1(ZNF469):c.11714C>G (p.Pro3905Arg) rs529322092
NM_001367624.1(ZNF469):c.11752G>A (p.Glu3918Lys) rs1085307510
NM_001367624.1(ZNF469):c.11809G>A (p.Gly3937Arg) rs886052421
NM_001367624.1(ZNF469):c.139G>A (p.Gly47Ser) rs138954293
NM_001367624.1(ZNF469):c.1483C>T (p.Pro495Ser) rs202205643
NM_001367624.1(ZNF469):c.1543G>A (p.Gly515Arg) rs1131691990
NM_001367624.1(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001367624.1(ZNF469):c.1654G>A (p.Gly552Arg) rs769955501
NM_001367624.1(ZNF469):c.1663G>A (p.Asp555Asn) rs749179728
NM_001367624.1(ZNF469):c.1781C>T (p.Pro594Leu) rs757534069
NM_001367624.1(ZNF469):c.1856G>T (p.Ser619Ile) rs1187845779
NM_001367624.1(ZNF469):c.186G>T (p.Glu62Asp) rs770775791
NM_001367624.1(ZNF469):c.2126C>T (p.Pro709Leu) rs1017679214
NM_001367624.1(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145
NM_001367624.1(ZNF469):c.2308C>T (p.Pro770Ser) rs1039078920
NM_001367624.1(ZNF469):c.2309C>T (p.Pro770Leu) rs1425767356
NM_001367624.1(ZNF469):c.2653C>G (p.Leu885Val) rs139653501
NM_001367624.1(ZNF469):c.2789G>T (p.Gly930Val) rs564654481
NM_001367624.1(ZNF469):c.3079C>A (p.Arg1027Ser) rs1057524853
NM_001367624.1(ZNF469):c.3109A>T (p.Arg1037Trp) rs753720576
NM_001367624.1(ZNF469):c.334G>A (p.Ala112Thr) rs766853024
NM_001367624.1(ZNF469):c.3452C>T (p.Ala1151Val) rs755348435
NM_001367624.1(ZNF469):c.3550G>A (p.Ala1184Thr) rs553460850
NM_001367624.1(ZNF469):c.3950A>G (p.Lys1317Arg) rs772817384
NM_001367624.1(ZNF469):c.4001C>T (p.Pro1334Leu) rs1016116935
NM_001367624.1(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076
NM_001367624.1(ZNF469):c.4609G>A (p.Gly1537Ser) rs528560466
NM_001367624.1(ZNF469):c.4771G>T (p.Ala1591Ser) rs755066385
NM_001367624.1(ZNF469):c.5158G>A (p.Val1720Ile) rs1131691303
NM_001367624.1(ZNF469):c.523G>A (p.Ala175Thr) rs1085307628
NM_001367624.1(ZNF469):c.5266G>A (p.Ala1756Thr) rs371328036
NM_001367624.1(ZNF469):c.5347G>A (p.Ala1783Thr) rs754873241
NM_001367624.1(ZNF469):c.536G>C (p.Gly179Ala) rs760014906
NM_001367624.1(ZNF469):c.5675G>A (p.Arg1892Lys) rs528085780
NM_001367624.1(ZNF469):c.578C>A (p.Ser193Tyr) rs1369047197
NM_001367624.1(ZNF469):c.585C>G (p.Asn195Lys) rs896312288
NM_001367624.1(ZNF469):c.5914G>A (p.Gly1972Arg) rs766410344
NM_001367624.1(ZNF469):c.6461C>T (p.Pro2154Leu) rs950986305
NM_001367624.1(ZNF469):c.6841G>A (p.Val2281Met) rs986749671
NM_001367624.1(ZNF469):c.6880G>A (p.Gly2294Arg) rs773187176
NM_001367624.1(ZNF469):c.6965T>C (p.Met2322Thr) rs531612776
NM_001367624.1(ZNF469):c.6978C>G (p.His2326Gln) rs185282301
NM_001367624.1(ZNF469):c.7267C>A (p.Pro2423Thr) rs199727372
NM_001367624.1(ZNF469):c.7466G>A (p.Arg2489Gln) rs547492890
NM_001367624.1(ZNF469):c.749T>A (p.Val250Asp) rs764273631
NM_001367624.1(ZNF469):c.7523C>T (p.Ala2508Val) rs570690992
NM_001367624.1(ZNF469):c.7574C>T (p.Pro2525Leu) rs756003807
NM_001367624.1(ZNF469):c.7611G>C (p.Glu2537Asp) rs199519673
NM_001367624.1(ZNF469):c.7628G>A (p.Arg2543Gln) rs771550262
NM_001367624.1(ZNF469):c.80C>T (p.Pro27Leu) rs1009769670
NM_001367624.1(ZNF469):c.8344C>T (p.His2782Tyr) rs553227769
NM_001367624.1(ZNF469):c.8381C>T (p.Thr2794Met) rs202188220
NM_001367624.1(ZNF469):c.8438C>G (p.Thr2813Ser) rs985304000
NM_001367624.1(ZNF469):c.8599G>A (p.Gly2867Ser) rs745468033
NM_001367624.1(ZNF469):c.8762G>A (p.Cys2921Tyr) rs1029645463
NM_001367624.1(ZNF469):c.8788G>T (p.Asp2930Tyr) rs76792613
NM_001367624.1(ZNF469):c.8984C>T (p.Ala2995Val) rs759398721
NM_001367624.1(ZNF469):c.9079C>T (p.Arg3027Cys) rs376513000
NM_001367624.1(ZNF469):c.9245C>T (p.Ala3082Val) rs1015869921
NM_001367624.1(ZNF469):c.9316C>T (p.Arg3106Trp) rs1292941352
NM_001367624.1(ZNF469):c.9335G>A (p.Arg3112Gln) rs942909542
NM_001367624.1(ZNF469):c.9368G>A (p.Arg3123His) rs536601676
NM_001367624.1(ZNF469):c.9448G>A (p.Glu3150Lys) rs777096338
NM_001367624.1(ZNF469):c.9622C>T (p.Arg3208Trp) rs936945500
NM_001367624.1(ZNF469):c.9676C>A (p.His3226Asn) rs867530230
NM_001367624.1(ZNF469):c.9833C>A (p.Thr3278Asn) rs571738263
NM_001367624.1(ZNF469):c.9850G>A (p.Gly3284Arg) rs773064083
NM_001367624.1(ZNF469):c.992C>T (p.Ala331Val) rs149485731

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