ClinVar Miner

List of variants in gene TET2 studied for not specified

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001127208.3(TET2):c.5284A>G (p.Ile1762Val) rs2454206 0.26430
NM_001127208.3(TET2):c.5162T>G (p.Leu1721Trp) rs34402524 0.11691
NM_001127208.3(TET2):c.652G>A (p.Val218Met) rs6843141 0.10516
NM_001127208.3(TET2):c.5333A>G (p.His1778Arg) rs62621450 0.08307
NM_001127208.3(TET2):c.1088C>T (p.Pro363Leu) rs17253672 0.04445
NM_001127208.3(TET2):c.86C>G (p.Pro29Arg) rs12498609 0.03467
NM_001127208.3(TET2):c.1064G>A (p.Gly355Asp) rs61744960 0.02834
NM_001127208.3(TET2):c.100C>T (p.Leu34Phe) rs111948941 0.01368
NM_001127208.3(TET2):c.2771A>G (p.His924Arg) rs34485921 0.00733
NM_001127208.3(TET2):c.2599T>C (p.Tyr867His) rs144386291 0.00675
NM_001127208.3(TET2):c.5167C>T (p.Pro1723Ser) rs146348065 0.00671
NM_001127208.3(TET2):c.5152G>T (p.Val1718Leu) rs142312318 0.00448
NM_001127208.3(TET2):c.5103G>A (p.Met1701Ile) rs62623390 0.00397
NM_001127208.3(TET2):c.3251A>C (p.Gln1084Pro) rs75056899 0.00305
NM_001127208.3(TET2):c.434G>A (p.Ser145Asn) rs114619974 0.00223
NM_001127208.3(TET2):c.5449C>A (p.His1817Asn) rs141442603 0.00218
NM_001127208.3(TET2):c.3409+18A>G rs144467609 0.00188
NM_001127208.3(TET2):c.521C>A (p.Pro174His) rs146031219 0.00144
NM_001127208.3(TET2):c.2604T>G (p.Phe868Leu) rs147836249 0.00125
NM_001127208.3(TET2):c.1285G>A (p.Gly429Arg) rs201642693 0.00056
NM_001127208.3(TET2):c.3116C>T (p.Ser1039Leu) rs111678678 0.00046
NM_001127208.3(TET2):c.3409+70G>A rs367758008 0.00045
NM_001127208.3(TET2):c.2385C>T (p.Ser795=) rs112576862 0.00043
NM_001127208.3(TET2):c.5885C>T (p.Pro1962Leu) rs200971953 0.00039
NM_001127208.3(TET2):c.3409+15T>A rs192879693 0.00031
NM_001127208.3(TET2):c.2440C>T (p.Arg814Cys) rs192553789 0.00020
NM_001127208.3(TET2):c.1379C>T (p.Ser460Phe) rs376570662 0.00018
NM_001127208.3(TET2):c.3409+42G>T rs141975400 0.00018
NM_001127208.3(TET2):c.2199C>T (p.Ser733=) rs145194380 0.00011
NM_001127208.3(TET2):c.4715G>A (p.Arg1572Gln) rs201570239 0.00011
NM_001127208.3(TET2):c.1724C>T (p.Ala575Val) rs199640757 0.00009
NM_001127208.3(TET2):c.3035C>T (p.Pro1012Leu) rs587778707 0.00007
NM_001127208.3(TET2):c.3387T>C (p.Asp1129=) rs367980467 0.00006
NM_001127208.3(TET2):c.5305G>C (p.Ala1769Pro) rs539389221 0.00006
NM_001127208.3(TET2):c.920T>G (p.Leu307Arg) rs145125867 0.00005
NM_001127208.3(TET2):c.3028G>A (p.Glu1010Lys) rs1173700891 0.00004
NM_001127208.3(TET2):c.2549A>G (p.His850Arg) rs369370690 0.00003
NM_001127208.3(TET2):c.4965G>A (p.Pro1655=) rs755125847 0.00003
NM_001127208.3(TET2):c.5413A>T (p.Asn1805Tyr) rs970128585 0.00003
NM_001127208.3(TET2):c.5484G>A (p.Gln1828=) rs752744962 0.00003
NM_001127208.3(TET2):c.6004A>G (p.Ile2002Val) rs587778701 0.00003
NM_001127208.3(TET2):c.3825G>T (p.Gly1275=) rs372281360 0.00002
NM_001127208.3(TET2):c.1745A>G (p.Asn582Ser) rs587778705 0.00001
NM_001127208.3(TET2):c.1819G>A (p.Gly607Arg) rs587778708 0.00001
NM_001127208.3(TET2):c.3109G>A (p.Ala1037Thr) rs748334095 0.00001
NM_001127208.3(TET2):c.5453A>T (p.Lys1818Ile) rs587778700 0.00001
NM_001127208.3(TET2):c.5599A>G (p.Thr1867Ala) rs1731208938 0.00001
NM_001127208.3(TET2):c.-46-63ATAG[4] rs58201766
NM_001127208.3(TET2):c.1386T>C (p.Ser462=)
NM_001127208.3(TET2):c.1900T>C (p.Tyr634His)
NM_001127208.3(TET2):c.197T>C (p.Met66Thr) rs587778709
NM_001127208.3(TET2):c.2290dup (p.Gln764fs)
NM_001127208.3(TET2):c.2299A>G (p.Asn767Asp)
NM_001127208.3(TET2):c.2429A>G (p.Gln810Arg) rs28555446
NM_001127208.3(TET2):c.2633T>G (p.Leu878Arg) rs753055492
NM_001127208.3(TET2):c.3409+1136T>A
NM_001127208.3(TET2):c.3803+5G>A
NM_001127208.3(TET2):c.3887A>T (p.Asn1296Ile)
NM_001127208.3(TET2):c.4817G>C (p.Gly1606Ala) rs587778702
NM_001127208.3(TET2):c.4975T>C (p.Tyr1659His) rs2110313413
NM_001127208.3(TET2):c.5284A>T (p.Ile1762Leu) rs2454206
NM_001127208.3(TET2):c.528T>A (p.Asn176Lys)
NM_001127208.3(TET2):c.5914G>C (p.Ala1972Pro) rs587778703
NM_001127208.3(TET2):c.723G>T (p.Ala241=) rs534182742
NM_001127208.3(TET2):c.899A>G (p.Asp300Gly) rs587778706
NM_001127208.3(TET2):c.959AAC[1] (p.Gln321del) rs587778704

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