ClinVar Miner

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

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Gene type:
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Total variants: 97
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HGVS dbSNP
NM_001127464.2(ZNF469):c.11290_11291delGGinsT (p.Gly3764Cysfs) rs1555520574
NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=) rs273585633
NM_001367624.1(ZNF469):c.10328G>C (p.Gly3443Ala) rs140056980
NM_001367624.1(ZNF469):c.10328G>T (p.Gly3443Val) rs140056980
NM_001367624.1(ZNF469):c.10361G>A (p.Arg3454Gln) rs75288466
NM_001367624.1(ZNF469):c.10582G>A (p.Glu3528Lys) rs758708056
NM_001367624.1(ZNF469):c.10683C>T (p.Ala3561=) rs794727258
NM_001367624.1(ZNF469):c.10700G>A (p.Gly3567Glu) rs199610834
NM_001367624.1(ZNF469):c.1088C>T (p.Ser363Leu) rs771000169
NM_001367624.1(ZNF469):c.11107G>A (p.Val3703Met) rs151127652
NM_001367624.1(ZNF469):c.11277C>T (p.Ser3759=) rs372634401
NM_001367624.1(ZNF469):c.11278G>A (p.Glu3760Lys) rs547014159
NM_001367624.1(ZNF469):c.11425G>A (p.Glu3809Lys) rs201834513
NM_001367624.1(ZNF469):c.11771C>T (p.Thr3924Met) rs139259830
NM_001367624.1(ZNF469):c.1346C>T (p.Pro449Leu) rs1388799029
NM_001367624.1(ZNF469):c.1471G>A (p.Ala491Thr) rs117555121
NM_001367624.1(ZNF469):c.1483C>T (p.Pro495Ser) rs202205643
NM_001367624.1(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001367624.1(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001367624.1(ZNF469):c.2017G>A (p.Ala673Thr) rs770623245
NM_001367624.1(ZNF469):c.2270T>G (p.Leu757Arg) rs753664726
NM_001367624.1(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145
NM_001367624.1(ZNF469):c.248C>T (p.Pro83Leu) rs775103017
NM_001367624.1(ZNF469):c.2671G>T (p.Val891Leu) rs753481187
NM_001367624.1(ZNF469):c.2699C>T (p.Pro900Leu) rs273585618
NM_001367624.1(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481
NM_001367624.1(ZNF469):c.2841G>A (p.Arg947=) rs150435442
NM_001367624.1(ZNF469):c.3055C>T (p.Pro1019Ser) rs937180195
NM_001367624.1(ZNF469):c.362T>C (p.Ile121Thr) rs1555518437
NM_001367624.1(ZNF469):c.3759G>A (p.Ala1253=) rs543669472
NM_001367624.1(ZNF469):c.3931C>T (p.Pro1311Ser) rs187453092
NM_001367624.1(ZNF469):c.4422G>A (p.Ala1474=) rs368877287
NM_001367624.1(ZNF469):c.4427G>A (p.Arg1476Lys) rs763632522
NM_001367624.1(ZNF469):c.4472C>T (p.Thr1491Met) rs375045076
NM_001367624.1(ZNF469):c.4556C>T (p.Ser1519Leu) rs767278971
NM_001367624.1(ZNF469):c.457C>A (p.Pro153Thr) rs532620482
NM_001367624.1(ZNF469):c.457C>G (p.Pro153Ala) rs532620482
NM_001367624.1(ZNF469):c.4829G>A (p.Arg1610His) rs567038987
NM_001367624.1(ZNF469):c.4910G>A (p.Arg1637Gln) rs273585621
NM_001367624.1(ZNF469):c.4952A>G (p.Gln1651Arg) rs773925755
NM_001367624.1(ZNF469):c.5114C>T (p.Thr1705Ile) rs768667107
NM_001367624.1(ZNF469):c.5162G>T (p.Cys1721Phe) rs568197988
NM_001367624.1(ZNF469):c.5340C>G (p.Pro1780=) rs184374078
NM_001367624.1(ZNF469):c.5414C>A (p.Pro1805His) rs78446958
NM_001367624.1(ZNF469):c.5675G>A (p.Arg1892Lys) rs528085780
NM_001367624.1(ZNF469):c.6629T>C (p.Leu2210Pro) rs564413710
NM_001367624.1(ZNF469):c.7195C>T (p.Pro2399Ser) rs759032227
NM_001367624.1(ZNF469):c.725G>T (p.Ser242Ile) rs536586591
NM_001367624.1(ZNF469):c.725_726delinsTT (p.Ser242Ile) rs886043704
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.7487G>A (p.Arg2496Gln) rs878852985
NM_001367624.1(ZNF469):c.7553C>A (p.Pro2518His) rs201943633
NM_001367624.1(ZNF469):c.7831G>A (p.Glu2611Lys) rs281865151
NM_001367624.1(ZNF469):c.7981G>A (p.Gly2661Ser) rs138259179
NM_001367624.1(ZNF469):c.8344C>T (p.His2782Tyr) rs553227769
NM_001367624.1(ZNF469):c.8425C>G (p.Pro2809Ala) rs794727257
NM_001367624.1(ZNF469):c.8477A>G (p.Asp2826Gly) rs886043475
NM_001367624.1(ZNF469):c.8489G>C (p.Gly2830Ala) rs541325052
NM_001367624.1(ZNF469):c.8705C>T (p.Thr2902Met) rs536725615
NM_001367624.1(ZNF469):c.8788G>T (p.Asp2930Tyr) rs76792613
NM_001367624.1(ZNF469):c.8941G>T (p.Asp2981Tyr) rs1343847655
NM_001367624.1(ZNF469):c.9055G>A (p.Glu3019Lys) rs765339766
NM_001367624.1(ZNF469):c.9131C>T (p.Thr3044Met) rs273585626
NM_001367624.1(ZNF469):c.9373C>T (p.Arg3125Cys) rs543370102
NM_001367624.1(ZNF469):c.9516C>T (p.Ala3172=) rs577913880
NM_001367624.1(ZNF469):c.9663C>T (p.Ser3221=) rs1555520265
NM_001367624.1(ZNF469):c.98C>T (p.Pro33Leu) rs752770883
NM_001367624.1(ZNF469):c.9919A>G (p.Thr3307Ala) rs273585627
NM_001367624.2(ZNF469):c.10324del (p.Arg3442fs)
NM_001367624.2(ZNF469):c.10352G>A (p.Arg3451His) rs972190166
NM_001367624.2(ZNF469):c.11318G>A (p.Arg3773Gln)
NM_001367624.2(ZNF469):c.11545C>T (p.Arg3849Trp) rs770109867
NM_001367624.2(ZNF469):c.1339C>T (p.Pro447Ser) rs931930346
NM_001367624.2(ZNF469):c.1418G>A (p.Arg473Gln)
NM_001367624.2(ZNF469):c.1475G>A (p.Arg492Gln) rs919081661
NM_001367624.2(ZNF469):c.1522G>A (p.Ala508Thr) rs750005577
NM_001367624.2(ZNF469):c.1750G>A (p.Val584Met)
NM_001367624.2(ZNF469):c.216G>T (p.Glu72Asp)
NM_001367624.2(ZNF469):c.2332G>A (p.Ala778Thr) rs761152033
NM_001367624.2(ZNF469):c.3179G>T (p.Arg1060Met) rs1597208477
NM_001367624.2(ZNF469):c.4731G>C (p.Arg1577Ser)
NM_001367624.2(ZNF469):c.5332C>A (p.Pro1778Thr)
NM_001367624.2(ZNF469):c.5706A>G (p.Ile1902Met) rs1597210698
NM_001367624.2(ZNF469):c.5915G>T (p.Gly1972Val)
NM_001367624.2(ZNF469):c.5967C>T (p.Ala1989=) rs955767732
NM_001367624.2(ZNF469):c.7013G>A (p.Gly2338Asp) rs1597211750
NM_001367624.2(ZNF469):c.7090G>A (p.Ala2364Thr)
NM_001367624.2(ZNF469):c.7444C>T (p.Arg2482Cys)
NM_001367624.2(ZNF469):c.7645G>A (p.Val2549Ile) rs759325304
NM_001367624.2(ZNF469):c.7838G>C (p.Arg2613Pro) rs370285147
NM_001367624.2(ZNF469):c.8931C>G (p.His2977Gln)
NM_001367624.2(ZNF469):c.9088G>A (p.Gly3030Ser) rs773580012
NM_001367624.2(ZNF469):c.9234C>G (p.Phe3078Leu)
NM_001367624.2(ZNF469):c.9387G>C (p.Glu3129Asp)
NM_001367624.2(ZNF469):c.9730T>C (p.Ser3244Pro) rs1597213923
NM_001367624.2(ZNF469):c.9977C>A (p.Thr3326Asn)

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