ClinVar Miner

List of variants in gene ZNF469 studied for not provided

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Gene type:
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Total variants: 97
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HGVS dbSNP
GRCh37/hg19 16q24.2(chr16:88376480-88510688)x1
NM_001127464.2(ZNF469):c.10248delG (p.Arg3417Glyfs) rs764470052
NM_001127464.2(ZNF469):c.11290_11291delGGinsT (p.Gly3764Cysfs) rs1555520574
NM_001127464.2(ZNF469):c.1673del (p.Ala558Valfs) rs1064795080
NM_001127464.2(ZNF469):c.3034delG (p.Val1012Serfs) rs1555519050
NM_001127464.2(ZNF469):c.7554del (p.Ser2519Alafs) rs886039575
NM_001127464.2(ZNF469):c.9011_9025delTTCCCGGGAACACCC (p.Leu3004_Thr3008del) rs281865162
NM_001367624.1(ZNF469):c.10067T>G (p.Leu3356Arg) rs1064796800
NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=) rs273585633
NM_001367624.1(ZNF469):c.10332dup (p.Arg3445fs) rs764470052
NM_001367624.1(ZNF469):c.10361G>A (p.Arg3454Gln) rs75288466
NM_001367624.1(ZNF469):c.10518G>A (p.Pro3506=) rs376379111
NM_001367624.1(ZNF469):c.10582G>A (p.Glu3528Lys) rs758708056
NM_001367624.1(ZNF469):c.10656G>A (p.Pro3552=) rs191234581
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.10795G>T (p.Ala3599Ser) rs199760004
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.11496_11505del (p.Ser3833fs) rs1567517877
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.1994C>T (p.Pro665Leu) rs184583062
NM_001367624.1(ZNF469):c.19C>T (p.Arg7Ter) rs1004428835
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.2407G>T (p.Ala803Ser) rs113484918
NM_001367624.1(ZNF469):c.248C>T (p.Pro83Leu) rs775103017
NM_001367624.1(ZNF469):c.2666C>T (p.Ala889Val) rs145186655
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.3341G>T (p.Arg1114Leu) rs568046708
NM_001367624.1(ZNF469):c.362T>C (p.Ile121Thr) rs1555518437
NM_001367624.1(ZNF469):c.3650C>T (p.Pro1217Leu) rs115183769
NM_001367624.1(ZNF469):c.3759G>A (p.Ala1253=) rs543669472
NM_001367624.1(ZNF469):c.3773C>A (p.Ala1258Glu) rs141255631
NM_001367624.1(ZNF469):c.3931C>T (p.Pro1311Ser) rs187453092
NM_001367624.1(ZNF469):c.3950A>G (p.Lys1317Arg) rs772817384
NM_001367624.1(ZNF469):c.4363C>G (p.Leu1455Val) rs116532825
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.4778C>T (p.Ser1593Leu) rs768864900
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.498C>G (p.Leu166=) rs1555518472
NM_001367624.1(ZNF469):c.5087C>T (p.Pro1696Leu) rs115487796
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.5548C>A (p.Pro1850Thr) rs199932922
NM_001367624.1(ZNF469):c.5675G>A (p.Arg1892Lys) rs528085780
NM_001367624.1(ZNF469):c.6333C>T (p.Ala2111=) rs1039243677
NM_001367624.1(ZNF469):c.6444del (p.Gln2149fs) rs886044697
NM_001367624.1(ZNF469):c.6599C>T (p.Thr2200Ile) rs1465493306
NM_001367624.1(ZNF469):c.6629T>C (p.Leu2210Pro) rs564413710
NM_001367624.1(ZNF469):c.6664dup (p.Leu2222fs) rs1361564558
NM_001367624.1(ZNF469):c.6944C>G (p.Pro2315Arg) rs77490207
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.7487G>A (p.Arg2496Gln) rs878852985
NM_001367624.1(ZNF469):c.7553C>A (p.Pro2518His) rs201943633
NM_001367624.1(ZNF469):c.7675A>G (p.Lys2559Glu) rs146789160
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.9018C>T (p.Ala3006=) rs1048591670
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.9268C>T (p.Arg3090Ter) rs764139968
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.9673G>A (p.Ala3225Thr) rs1046436333
NM_001367624.1(ZNF469):c.9696G>A (p.Thr3232=) rs573582117
NM_001367624.1(ZNF469):c.98C>T (p.Pro33Leu) rs752770883
NM_001367624.1(ZNF469):c.9919A>G (p.Thr3307Ala) rs273585627

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