ClinVar Miner

List of variants in gene TET3 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
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.1020C>G (p.Ser340=) rs201715061 0.00062
NM_001287491.2(TET3):c.1307C>T (p.Ala436Val) rs201500476 0.00028
NM_001287491.2(TET3):c.5030C>T (p.Pro1677Leu) rs1691236972 0.00001
NM_001287491.2(TET3):c.1101C>T (p.Ser367=)
NM_001287491.2(TET3):c.1113G>A (p.Pro371=)
NM_001287491.2(TET3):c.1128C>T (p.Ser376=)
NM_001287491.2(TET3):c.1242C>T (p.His414=)
NM_001287491.2(TET3):c.1255C>A (p.Pro419Thr)
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.15G>C (p.Gln5His) rs2105056319
NM_001287491.2(TET3):c.1637C>T (p.Thr546Ile)
NM_001287491.2(TET3):c.1706G>A (p.Arg569Gln)
NM_001287491.2(TET3):c.1719A>G (p.Arg573=)
NM_001287491.2(TET3):c.1811G>A (p.Arg604Gln)
NM_001287491.2(TET3):c.1942C>T (p.Leu648=)
NM_001287491.2(TET3):c.2034C>T (p.Pro678=)
NM_001287491.2(TET3):c.2196T>A (p.Ile732=)
NM_001287491.2(TET3):c.254A>T (p.Lys85Ile)
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.2878C>T (p.Leu960Phe)
NM_001287491.2(TET3):c.2912A>C (p.Lys971Thr)
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.3225C>T (p.His1075=)
NM_001287491.2(TET3):c.3234_3235delinsC (p.Lys1078fs)
NM_001287491.2(TET3):c.3300C>T (p.Cys1100=)
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.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.3723G>A (p.Ser1241=)
NM_001287491.2(TET3):c.3741G>A (p.Arg1247=)
NM_001287491.2(TET3):c.3760A>G (p.Met1254Val)
NM_001287491.2(TET3):c.3847T>A (p.Ser1283Thr)
NM_001287491.2(TET3):c.3883G>A (p.Val1295Ile)
NM_001287491.2(TET3):c.4014C>T (p.Ala1338=)
NM_001287491.2(TET3):c.4116C>T (p.Ala1372=)
NM_001287491.2(TET3):c.4117C>G (p.Pro1373Ala)
NM_001287491.2(TET3):c.4219G>C (p.Ala1407Pro)
NM_001287491.2(TET3):c.4266G>C (p.Leu1422=)
NM_001287491.2(TET3):c.4269C>A (p.Ser1423=)
NM_001287491.2(TET3):c.4349A>C (p.Asn1450Thr)
NM_001287491.2(TET3):c.439C>A (p.Arg147=)
NM_001287491.2(TET3):c.4402G>A (p.Val1468Ile)
NM_001287491.2(TET3):c.4510T>C (p.Ser1504Pro)
NM_001287491.2(TET3):c.4602G>T (p.Pro1534=) rs371898753
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.4708G>A (p.Ala1570Thr)
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.5019C>T (p.His1673=)
NM_001287491.2(TET3):c.513G>C (p.Gly171=)
NM_001287491.2(TET3):c.5151G>A (p.Ala1717=)
NM_001287491.2(TET3):c.5206G>A (p.Glu1736Lys) rs2104235676
NM_001287491.2(TET3):c.5228A>G (p.Lys1743Arg)
NM_001287491.2(TET3):c.5325G>A (p.Ser1775=)
NM_001287491.2(TET3):c.5353A>C (p.Thr1785Pro)
NM_001287491.2(TET3):c.648T>C (p.Leu216=)
NM_001287491.2(TET3):c.818A>G (p.Asn273Ser) rs2103678064
NM_001287491.2(TET3):c.879G>A (p.Val293=)
NM_001287491.2(TET3):c.948A>G (p.Pro316=)

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