ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
Download table as spreadsheet
HGVS dbSNP
NM_001127464.2(ZNF469):c.1020C>T (p.Gly340=) rs273585633
NM_001127464.2(ZNF469):c.10277G>A (p.Arg3426Gln) rs75288466
NM_001127464.2(ZNF469):c.10498G>A (p.Glu3500Lys) rs758708056
NM_001127464.2(ZNF469):c.10599C>T (p.Ala3533=) rs794727258
NM_001127464.2(ZNF469):c.10616G>A (p.Gly3539Glu) rs199610834
NM_001127464.2(ZNF469):c.1088C>T (p.Ser363Leu) rs771000169
NM_001127464.2(ZNF469):c.11023G>A (p.Val3675Met) rs151127652
NM_001127464.2(ZNF469):c.11193C>T (p.Ser3731=) rs372634401
NM_001127464.2(ZNF469):c.11194G>A (p.Glu3732Lys) rs547014159
NM_001127464.2(ZNF469):c.11290_11291delGGinsT (p.Gly3764Cysfs) rs1555520574
NM_001127464.2(ZNF469):c.11687C>T (p.Thr3896Met) rs139259830
NM_001127464.2(ZNF469):c.1346C>T (p.Pro449Leu) rs1388799029
NM_001127464.2(ZNF469):c.1471G>A (p.Ala491Thr) rs117555121
NM_001127464.2(ZNF469):c.1483C>T (p.Pro495Ser) rs202205643
NM_001127464.2(ZNF469):c.1609G>A (p.Val537Met) rs184458982
NM_001127464.2(ZNF469):c.1615A>T (p.Ser539Cys) rs189476639
NM_001127464.2(ZNF469):c.1994C>T (p.Pro665Leu) rs184583062
NM_001127464.2(ZNF469):c.2017G>A (p.Ala673Thr) rs770623245
NM_001127464.2(ZNF469):c.2270T>G (p.Leu757Arg) rs753664726
NM_001127464.2(ZNF469):c.2297G>A (p.Arg766Gln) rs144492145
NM_001127464.2(ZNF469):c.248C>T (p.Pro83Leu) rs775103017
NM_001127464.2(ZNF469):c.2671G>T (p.Val891Leu) rs753481187
NM_001127464.2(ZNF469):c.2699C>T (p.Pro900Leu) rs273585618
NM_001127464.2(ZNF469):c.2717C>T (p.Pro906Leu) rs77951481
NM_001127464.2(ZNF469):c.2841G>A (p.Arg947=) rs150435442
NM_001127464.2(ZNF469):c.3055C>T (p.Pro1019Ser) rs937180195
NM_001127464.2(ZNF469):c.362T>C (p.Ile121Thr) rs1555518437
NM_001127464.2(ZNF469):c.3675G>A (p.Ala1225=) rs543669472
NM_001127464.2(ZNF469):c.3847C>T (p.Pro1283Ser) rs187453092
NM_001127464.2(ZNF469):c.4338G>A (p.Ala1446=) rs368877287
NM_001127464.2(ZNF469):c.4343G>A (p.Arg1448Lys) rs763632522
NM_001127464.2(ZNF469):c.4388C>T (p.Thr1463Met) rs375045076
NM_001127464.2(ZNF469):c.4472C>T (p.Ser1491Leu) rs767278971
NM_001127464.2(ZNF469):c.457C>A (p.Pro153Thr) rs532620482
NM_001127464.2(ZNF469):c.457C>G (p.Pro153Ala) rs532620482
NM_001127464.2(ZNF469):c.4745G>A (p.Arg1582His) rs567038987
NM_001127464.2(ZNF469):c.4868A>G (p.Gln1623Arg) rs773925755
NM_001127464.2(ZNF469):c.5078G>T (p.Cys1693Phe) rs568197988
NM_001127464.2(ZNF469):c.5256C>G (p.Pro1752=) rs184374078
NM_001127464.2(ZNF469):c.5330C>A (p.Pro1777His) rs78446958
NM_001127464.2(ZNF469):c.5591G>A (p.Arg1864Lys) rs528085780
NM_001127464.2(ZNF469):c.6545T>C (p.Leu2182Pro) rs564413710
NM_001127464.2(ZNF469):c.7183C>A (p.Pro2395Thr) rs199727372
NM_001127464.2(ZNF469):c.725G>T (p.Ser242Ile) rs536586591
NM_001127464.2(ZNF469):c.725_726delGCinsTT (p.Ser242Ile) rs886043704
NM_001127464.2(ZNF469):c.7403G>A (p.Arg2468Gln) rs878852985
NM_001127464.2(ZNF469):c.7469C>A (p.Pro2490His) rs201943633
NM_001127464.2(ZNF469):c.7747G>A (p.Glu2583Lys) rs281865151
NM_001127464.2(ZNF469):c.7897G>A (p.Gly2633Ser) rs138259179
NM_001127464.2(ZNF469):c.8260C>T (p.His2754Tyr) rs553227769
NM_001127464.2(ZNF469):c.8341C>G (p.Pro2781Ala) rs794727257
NM_001127464.2(ZNF469):c.8393A>G (p.Asp2798Gly) rs886043475
NM_001127464.2(ZNF469):c.8405G>C (p.Gly2802Ala) rs541325052
NM_001127464.2(ZNF469):c.8621C>T (p.Thr2874Met) rs536725615
NM_001127464.2(ZNF469):c.8704G>T (p.Asp2902Tyr) rs76792613
NM_001127464.2(ZNF469):c.8857G>T (p.Asp2953Tyr) rs1343847655
NM_001127464.2(ZNF469):c.9047C>T (p.Thr3016Met) rs273585626
NM_001127464.2(ZNF469):c.9432C>T (p.Ala3144=) rs577913880
NM_001127464.2(ZNF469):c.9579C>T (p.Ser3193=) rs1555520265
NM_001127464.2(ZNF469):c.9835A>G (p.Thr3279Ala) rs273585627
NM_001127464.2(ZNF469):c.98C>T (p.Pro33Leu) rs752770883
NM_001367624.1(ZNF469):c.4910G>A (p.Arg1637Gln)
NM_001367624.1(ZNF469):c.9055G>A (p.Glu3019Lys)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.