ClinVar Miner

List of variants in gene TET3 studied for not provided

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Gene type:
ClinVar version:
Total variants: 211
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HGVS dbSNP gnomAD frequency
NM_001287491.2(TET3):c.2536T>C (p.Leu846=) rs7560668 0.39767
NM_001287491.2(TET3):c.4524G>C (p.Leu1508=) rs60481444 0.05465
NM_001287491.2(TET3):c.1285C>T (p.Pro429Ser) rs61741171 0.04165
NM_001287491.2(TET3):c.5172G>A (p.Gln1724=) rs79170439 0.02799
NM_001287491.2(TET3):c.4959C>T (p.Gly1653=) rs116688476 0.01923
NM_001287491.2(TET3):c.1371C>T (p.Pro457=) rs61742889 0.01009
NM_001287491.2(TET3):c.1700T>C (p.Val567Ala) rs148646838 0.00702
NM_001287491.2(TET3):c.360+47G>A rs185515634 0.00469
NM_001287491.2(TET3):c.1934C>T (p.Pro645Leu) rs201583228 0.00447
NM_001287491.2(TET3):c.2805C>T (p.Leu935=) rs115293949 0.00329
NM_001287491.2(TET3):c.2135G>A (p.Arg712Gln) rs57955681 0.00188
NM_001287491.2(TET3):c.4483G>A (p.Gly1495Ser) rs201927778 0.00156
NM_001287491.2(TET3):c.1020C>G (p.Ser340=) rs201715061 0.00062
NM_001287491.2(TET3):c.79G>A (p.Val27Ile) rs142623499 0.00047
NM_001287491.2(TET3):c.1307C>T (p.Ala436Val) rs201500476 0.00028
NM_001287491.2(TET3):c.2254C>T (p.Arg752Cys) rs534089911 0.00008
NM_001287491.2(TET3):c.1395G>T (p.Gln465His) rs747719049 0.00001
NM_001287491.2(TET3):c.1690A>T (p.Ser564Cys) rs751119029 0.00001
NM_001287491.2(TET3):c.2597A>G (p.Lys866Arg) rs957551558 0.00001
NM_001287491.2(TET3):c.5030C>T (p.Pro1677Leu) rs1691236972 0.00001
NC_000002.11:g.(?_74307117)_(74307868_?)del
NM_001287491.2(TET3):c.1101C>T (p.Ser367=)
NM_001287491.2(TET3):c.1113G>A (p.Pro371=)
NM_001287491.2(TET3):c.1117_1122delinsTTC (p.Pro373_Ser374delinsPhe)
NM_001287491.2(TET3):c.1128C>T (p.Ser376=)
NM_001287491.2(TET3):c.1183A>G (p.Arg395Gly)
NM_001287491.2(TET3):c.1189C>G (p.Pro397Ala) rs375606763
NM_001287491.2(TET3):c.1228C>T (p.Pro410Ser)
NM_001287491.2(TET3):c.1242C>T (p.His414=)
NM_001287491.2(TET3):c.1252G>C (p.Ala418Pro)
NM_001287491.2(TET3):c.1255C>A (p.Pro419Thr)
NM_001287491.2(TET3):c.1255C>T (p.Pro419Ser)
NM_001287491.2(TET3):c.1339C>T (p.Arg447Trp)
NM_001287491.2(TET3):c.139_140dup (p.Gly48fs)
NM_001287491.2(TET3):c.1496C>T (p.Pro499Leu) rs200362611
NM_001287491.2(TET3):c.1497GGCCCC[3] (p.Pro503_Ser504insAlaPro)
NM_001287491.2(TET3):c.1503G>C (p.Pro501=)
NM_001287491.2(TET3):c.1536C>T (p.Pro512=)
NM_001287491.2(TET3):c.1542A>C (p.Pro514=)
NM_001287491.2(TET3):c.1553C>T (p.Pro518Leu)
NM_001287491.2(TET3):c.1565A>G (p.Gln522Arg)
NM_001287491.2(TET3):c.15G>C (p.Gln5His) rs2105056319
NM_001287491.2(TET3):c.1637C>T (p.Thr546Ile)
NM_001287491.2(TET3):c.1677G>T (p.Trp559Cys)
NM_001287491.2(TET3):c.1706G>A (p.Arg569Gln)
NM_001287491.2(TET3):c.1719A>G (p.Arg573=)
NM_001287491.2(TET3):c.1721C>T (p.Pro574Leu)
NM_001287491.2(TET3):c.1724C>A (p.Pro575His)
NM_001287491.2(TET3):c.1736A>G (p.Lys579Arg)
NM_001287491.2(TET3):c.174dup (p.Thr59fs)
NM_001287491.2(TET3):c.1811G>A (p.Arg604Gln)
NM_001287491.2(TET3):c.1858C>G (p.Leu620Val)
NM_001287491.2(TET3):c.190C>T (p.Arg64Trp)
NM_001287491.2(TET3):c.1942C>T (p.Leu648=)
NM_001287491.2(TET3):c.1994C>T (p.Ala665Val)
NM_001287491.2(TET3):c.2003C>T (p.Ala668Val)
NM_001287491.2(TET3):c.2034C>T (p.Pro678=)
NM_001287491.2(TET3):c.207_208del (p.Cys69fs)
NM_001287491.2(TET3):c.2089A>G (p.Thr697Ala)
NM_001287491.2(TET3):c.2115C>G (p.Asp705Glu)
NM_001287491.2(TET3):c.2135G>C (p.Arg712Pro)
NM_001287491.2(TET3):c.2196T>A (p.Ile732=)
NM_001287491.2(TET3):c.2321A>G (p.His774Arg)
NM_001287491.2(TET3):c.2437C>G (p.Leu813Val)
NM_001287491.2(TET3):c.2462C>A (p.Ala821Asp)
NM_001287491.2(TET3):c.2533C>T (p.His845Tyr)
NM_001287491.2(TET3):c.2543C>T (p.Ser848Phe)
NM_001287491.2(TET3):c.2549C>T (p.Pro850Leu) rs2103939816
NM_001287491.2(TET3):c.254A>T (p.Lys85Ile)
NM_001287491.2(TET3):c.2576T>C (p.Met859Thr)
NM_001287491.2(TET3):c.2611C>T (p.Arg871Trp)
NM_001287491.2(TET3):c.2612G>A (p.Arg871Gln)
NM_001287491.2(TET3):c.2612G>T (p.Arg871Leu) rs1188197678
NM_001287491.2(TET3):c.2616C>G (p.Ile872Met)
NM_001287491.2(TET3):c.2652C>A (p.Ser884Arg)
NM_001287491.2(TET3):c.2716T>G (p.Cys906Gly)
NM_001287491.2(TET3):c.2725C>T (p.Arg909Trp)
NM_001287491.2(TET3):c.2731C>G (p.Arg911Gly) rs1690250283
NM_001287491.2(TET3):c.2732G>A (p.Arg911Gln) rs2104065629
NM_001287491.2(TET3):c.2754C>T (p.Asn918=)
NM_001287491.2(TET3):c.2855A>G (p.Asn952Ser) rs1573892799
NM_001287491.2(TET3):c.285A>G (p.Lys95=)
NM_001287491.2(TET3):c.2876G>T (p.Gly959Val)
NM_001287491.2(TET3):c.2878C>T (p.Leu960Phe)
NM_001287491.2(TET3):c.2912A>C (p.Lys971Thr)
NM_001287491.2(TET3):c.3001C>T (p.Pro1001Ser)
NM_001287491.2(TET3):c.3004C>A (p.Arg1002Ser) rs1690385290
NM_001287491.2(TET3):c.3004C>T (p.Arg1002Cys)
NM_001287491.2(TET3):c.303G>A (p.Glu101=) rs1573616190
NM_001287491.2(TET3):c.3084C>T (p.Val1028=)
NM_001287491.2(TET3):c.3100C>T (p.Arg1034Ter) rs2104122592
NM_001287491.2(TET3):c.3117C>T (p.Ala1039=)
NM_001287491.2(TET3):c.3139G>A (p.Glu1047Lys)
NM_001287491.2(TET3):c.3161G>A (p.Arg1054His)
NM_001287491.2(TET3):c.3167G>A (p.Gly1056Glu)
NM_001287491.2(TET3):c.3200C>T (p.Thr1067Met)
NM_001287491.2(TET3):c.3225C>T (p.His1075=)
NM_001287491.2(TET3):c.3234_3235delinsC (p.Lys1078fs)
NM_001287491.2(TET3):c.3267+1G>A
NM_001287491.2(TET3):c.3300C>T (p.Cys1100=)
NM_001287491.2(TET3):c.3341C>T (p.Pro1114Leu)
NM_001287491.2(TET3):c.3378C>T (p.Ser1126=)
NM_001287491.2(TET3):c.3409G>A (p.Gly1137Arg)
NM_001287491.2(TET3):c.3423G>A (p.Val1141=)
NM_001287491.2(TET3):c.3423G>T (p.Val1141=)
NM_001287491.2(TET3):c.3429C>T (p.Thr1143=)
NM_001287491.2(TET3):c.3448C>T (p.Arg1150Ter)
NM_001287491.2(TET3):c.3473C>T (p.Ser1158Phe)
NM_001287491.2(TET3):c.3484C>T (p.Arg1162Trp)
NM_001287491.2(TET3):c.3574C>G (p.Leu1192Val)
NM_001287491.2(TET3):c.3597G>A (p.Ser1199=)
NM_001287491.2(TET3):c.3624A>G (p.Gly1208=)
NM_001287491.2(TET3):c.3638G>A (p.Gly1213Asp)
NM_001287491.2(TET3):c.3657G>C (p.Lys1219Asn)
NM_001287491.2(TET3):c.3713A>C (p.Glu1238Ala)
NM_001287491.2(TET3):c.3723G>A (p.Ser1241=)
NM_001287491.2(TET3):c.372G>C (p.Glu124Asp)
NM_001287491.2(TET3):c.3741G>A (p.Arg1247=)
NM_001287491.2(TET3):c.3760A>G (p.Met1254Val)
NM_001287491.2(TET3):c.3814G>C (p.Val1272Leu)
NM_001287491.2(TET3):c.3833A>G (p.Lys1278Arg)
NM_001287491.2(TET3):c.3847T>A (p.Ser1283Thr)
NM_001287491.2(TET3):c.3879C>A (p.Asn1293Lys)
NM_001287491.2(TET3):c.3883G>A (p.Val1295Ile)
NM_001287491.2(TET3):c.3904G>A (p.Gly1302Ser)
NM_001287491.2(TET3):c.3967G>T (p.Ala1323Ser)
NM_001287491.2(TET3):c.3977A>G (p.Asn1326Ser)
NM_001287491.2(TET3):c.4001G>T (p.Gly1334Val)
NM_001287491.2(TET3):c.4014C>T (p.Ala1338=)
NM_001287491.2(TET3):c.4017G>C (p.Glu1339Asp)
NM_001287491.2(TET3):c.4090C>T (p.Pro1364Ser) rs1691163236
NM_001287491.2(TET3):c.4116C>T (p.Ala1372=)
NM_001287491.2(TET3):c.4117C>G (p.Pro1373Ala)
NM_001287491.2(TET3):c.4144C>A (p.Pro1382Thr)
NM_001287491.2(TET3):c.4195G>A (p.Glu1399Lys)
NM_001287491.2(TET3):c.4214C>A (p.Thr1405Asn)
NM_001287491.2(TET3):c.4219G>C (p.Ala1407Pro)
NM_001287491.2(TET3):c.4229T>C (p.Val1410Ala)
NM_001287491.2(TET3):c.4241C>T (p.Ala1414Val)
NM_001287491.2(TET3):c.4262C>T (p.Pro1421Leu)
NM_001287491.2(TET3):c.4266G>C (p.Leu1422=)
NM_001287491.2(TET3):c.4269C>A (p.Ser1423=)
NM_001287491.2(TET3):c.4288G>A (p.Gly1430Arg)
NM_001287491.2(TET3):c.4349A>C (p.Asn1450Thr)
NM_001287491.2(TET3):c.4357G>A (p.Gly1453Ser)
NM_001287491.2(TET3):c.439C>A (p.Arg147=)
NM_001287491.2(TET3):c.4402G>A (p.Val1468Ile)
NM_001287491.2(TET3):c.4414C>T (p.Leu1472Phe) rs1691188315
NM_001287491.2(TET3):c.4421C>T (p.Ser1474Phe)
NM_001287491.2(TET3):c.4439T>G (p.Leu1480Arg)
NM_001287491.2(TET3):c.4441G>T (p.Ala1481Ser)
NM_001287491.2(TET3):c.4463G>T (p.Gly1488Val)
NM_001287491.2(TET3):c.4472G>T (p.Gly1491Val)
NM_001287491.2(TET3):c.4475T>C (p.Leu1492Pro)
NM_001287491.2(TET3):c.4492_4497del (p.Gln1498_Gln1499del)
NM_001287491.2(TET3):c.4510T>C (p.Ser1504Pro)
NM_001287491.2(TET3):c.4580G>A (p.Gly1527Glu)
NM_001287491.2(TET3):c.4602G>T (p.Pro1534=) rs371898753
NM_001287491.2(TET3):c.4607C>T (p.Ala1536Val)
NM_001287491.2(TET3):c.4608G>A (p.Ala1536=)
NM_001287491.2(TET3):c.4617A>C (p.Ala1539=)
NM_001287491.2(TET3):c.4686A>G (p.Gly1562=)
NM_001287491.2(TET3):c.4705G>C (p.Ala1569Pro)
NM_001287491.2(TET3):c.4708G>A (p.Ala1570Thr)
NM_001287491.2(TET3):c.4740G>C (p.Gln1580His)
NM_001287491.2(TET3):c.4742C>T (p.Ser1581Phe)
NM_001287491.2(TET3):c.4745T>A (p.Phe1582Tyr) rs1691216225
NM_001287491.2(TET3):c.4780G>A (p.Gly1594Arg)
NM_001287491.2(TET3):c.4818C>G (p.Phe1606Leu)
NM_001287491.2(TET3):c.4846C>T (p.Pro1616Ser)
NM_001287491.2(TET3):c.4881C>T (p.Gly1627=)
NM_001287491.2(TET3):c.4893G>A (p.Ala1631=)
NM_001287491.2(TET3):c.4980C>T (p.His1660=)
NM_001287491.2(TET3):c.5006G>A (p.Arg1669Gln)
NM_001287491.2(TET3):c.5019C>T (p.His1673=)
NM_001287491.2(TET3):c.5045A>G (p.Asn1682Ser)
NM_001287491.2(TET3):c.5048G>A (p.Arg1683His)
NM_001287491.2(TET3):c.5062C>G (p.Arg1688Gly) rs2104233612
NM_001287491.2(TET3):c.5065A>G (p.Ile1689Val)
NM_001287491.2(TET3):c.5069C>T (p.Ser1690Leu) rs2104233688
NM_001287491.2(TET3):c.5110C>T (p.His1704Tyr)
NM_001287491.2(TET3):c.5112C>G (p.His1704Gln)
NM_001287491.2(TET3):c.5121_5122dup (p.Leu1708fs) rs2104234030
NM_001287491.2(TET3):c.513G>C (p.Gly171=)
NM_001287491.2(TET3):c.5151G>A (p.Ala1717=)
NM_001287491.2(TET3):c.518C>T (p.Pro173Leu)
NM_001287491.2(TET3):c.5206G>A (p.Glu1736Lys) rs2104235676
NM_001287491.2(TET3):c.5214G>C (p.Lys1738Asn) rs1691249064
NM_001287491.2(TET3):c.5228A>G (p.Lys1743Arg)
NM_001287491.2(TET3):c.5237G>C (p.Trp1746Ser)
NM_001287491.2(TET3):c.5237G>T (p.Trp1746Leu) rs190925009
NM_001287491.2(TET3):c.5254G>C (p.Ala1752Pro)
NM_001287491.2(TET3):c.5264A>C (p.Gln1755Pro)
NM_001287491.2(TET3):c.5266C>G (p.Gln1756Glu) rs1389497450
NM_001287491.2(TET3):c.5325G>A (p.Ser1775=)
NM_001287491.2(TET3):c.5344T>C (p.Tyr1782His) rs1196419881
NM_001287491.2(TET3):c.5353A>C (p.Thr1785Pro)
NM_001287491.2(TET3):c.648T>C (p.Leu216=)
NM_001287491.2(TET3):c.655C>T (p.Arg219Trp)
NM_001287491.2(TET3):c.679G>A (p.Glu227Lys) rs2103675806
NM_001287491.2(TET3):c.72G>T (p.Gln24His)
NM_001287491.2(TET3):c.79G>C (p.Val27Leu)
NM_001287491.2(TET3):c.7C>T (p.Gln3Ter)
NM_001287491.2(TET3):c.806C>T (p.Pro269Leu)
NM_001287491.2(TET3):c.818A>G (p.Asn273Ser) rs2103678064
NM_001287491.2(TET3):c.879G>A (p.Val293=)
NM_001287491.2(TET3):c.881_882delinsCA (p.Val294Ala)
NM_001287491.2(TET3):c.905C>T (p.Pro302Leu)
NM_001287491.2(TET3):c.914C>T (p.Pro305Leu) rs2103679574
NM_001287491.2(TET3):c.946C>T (p.Pro316Ser)
NM_001287491.2(TET3):c.948A>G (p.Pro316=)

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