ClinVar Miner

List of variants in gene TCF4 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.1070-73G>A rs74849864 0.03500
NM_001083962.2(TCF4):c.500-88G>A rs147845905 0.02315
NM_001083962.2(TCF4):c.923-43G>A rs35918540 0.02297
NM_001083962.2(TCF4):c.*5-68T>A rs185507582 0.02264
NM_001083962.2(TCF4):c.207+128G>C rs766637597 0.01917
NM_001083962.2(TCF4):c.*53C>A rs111947783 0.01565
NM_001083962.2(TCF4):c.*5-62A>G rs115906079 0.01441
NM_001083962.2(TCF4):c.1880-132C>T rs144033370 0.01317
NM_001083962.2(TCF4):c.500-232A>G rs75329899 0.01192
NM_001083962.2(TCF4):c.207+94C>G rs549984245 0.00983
NM_001083962.2(TCF4):c.369+243C>T rs9965322 0.00953
NM_001083962.2(TCF4):c.370-243A>T rs115898885 0.00738
NM_001083962.2(TCF4):c.1069+122T>A rs74562156 0.00515
NM_001083962.2(TCF4):c.1070-202T>A rs112454654 0.00371
NM_001083962.2(TCF4):c.1879+32G>A rs114215910 0.00332
NM_001083962.2(TCF4):c.146-275A>T rs140065907 0.00309
NM_001083962.2(TCF4):c.1905G>A (p.Ala635=) rs151150677 0.00274
NM_001083962.2(TCF4):c.73-3T>C rs148658897 0.00182
NM_001083962.2(TCF4):c.1419G>C (p.Pro473=) rs143944746 0.00178
NM_001083962.2(TCF4):c.*3404G>C rs550785276 0.00153
NM_001083962.2(TCF4):c.923-27T>G rs368057502 0.00131
NM_001083962.2(TCF4):c.*452T>G rs541527476 0.00077
NM_001083962.2(TCF4):c.1923G>A (p.Glu641=) rs76956936 0.00067
NM_001083962.2(TCF4):c.269A>G (p.Asn90Ser) rs143244149 0.00067
NM_001083962.2(TCF4):c.944C>T (p.Ala315Val) rs147445499 0.00066
NM_001083962.2(TCF4):c.1577C>T (p.Thr526Met) rs202025804 0.00051
NM_001083962.2(TCF4):c.936C>T (p.Ser312=) rs368270265 0.00043
NM_001083962.2(TCF4):c.504A>G (p.Val168=) rs370160994 0.00037
NM_001083962.2(TCF4):c.966T>C (p.Asp322=) rs142998298 0.00034
NM_001083962.2(TCF4):c.1487-5G>A rs749176054 0.00016
NM_001083962.2(TCF4):c.1545C>T (p.Ser515=) rs777418647 0.00012
NM_001083962.2(TCF4):c.1551C>T (p.Asp517=) rs140862252 0.00012
NM_001083962.2(TCF4):c.1866G>A (p.Glu622=) rs140078086 0.00006
NM_001083962.2(TCF4):c.1283G>T (p.Gly428Val) rs186508321 0.00004
NM_001083962.2(TCF4):c.240G>A (p.Met80Ile) rs532294589 0.00004
NM_001083962.2(TCF4):c.594G>A (p.Ser198=) rs368553922 0.00004
NM_001243226.3(TCF4):c.239C>T (p.Thr80Met) rs918143909 0.00004
NM_001083962.2(TCF4):c.1317C>T (p.Thr439=) rs200112082 0.00003
NM_001083962.2(TCF4):c.1608C>T (p.Asp536=) rs370405835 0.00003
NM_001083962.2(TCF4):c.1965C>T (p.Ala655=) rs147289056 0.00003
NM_001083962.2(TCF4):c.466C>A (p.Pro156Thr) rs200889338 0.00003
NM_001083962.2(TCF4):c.550-8C>A rs748083315 0.00003
NM_001083962.2(TCF4):c.1032C>T (p.Asn344=) rs372738049 0.00001
NM_001083962.2(TCF4):c.1185T>C (p.Asp395=) rs1341306301 0.00001
NM_001083962.2(TCF4):c.1989C>T (p.Asp663=) rs752325141 0.00001
NM_001083962.2(TCF4):c.584A>G (p.Asn195Ser) rs148573556 0.00001
NM_001083962.2(TCF4):c.*266C>G
NM_001083962.2(TCF4):c.*3397T>A
NM_001083962.2(TCF4):c.-41G>A rs1603624917
NM_001083962.2(TCF4):c.1026A>G (p.Ser342=)
NM_001083962.2(TCF4):c.1056T>A (p.Pro352=)
NM_001083962.2(TCF4):c.1065C>G (p.Leu355=)
NM_001083962.2(TCF4):c.1069+30A>G rs143555588
NM_001083962.2(TCF4):c.1265T>C (p.Ile422Thr) rs1555764219
NM_001083962.2(TCF4):c.1299G>A (p.Leu433=) rs552340151
NM_001083962.2(TCF4):c.1395T>C (p.His465=) rs1599574599
NM_001083962.2(TCF4):c.146-136A>T rs144919408
NM_001083962.2(TCF4):c.1501C>T (p.Leu501=) rs781382144
NM_001083962.2(TCF4):c.1503A>G (p.Leu501=)
NM_001083962.2(TCF4):c.1593C>T (p.Asp531=)
NM_001083962.2(TCF4):c.1608C>G (p.Asp536Glu)
NM_001083962.2(TCF4):c.180G>T (p.Gly60=)
NM_001083962.2(TCF4):c.201G>A (p.Pro67=) rs775657966
NM_001083962.2(TCF4):c.207+129_207+130insAC rs1491179811
NM_001083962.2(TCF4):c.207+97_207+102del rs200413459
NM_001083962.2(TCF4):c.207+98CA[11] rs151196106
NM_001083962.2(TCF4):c.207+98CA[16] rs151196106
NM_001083962.2(TCF4):c.207+98_207+99insCTCACA rs867214369
NM_001083962.2(TCF4):c.207+98_207+99insCTCTCA rs867214369
NM_001083962.2(TCF4):c.305-150G>A
NM_001083962.2(TCF4):c.305-53dup rs551539799
NM_001083962.2(TCF4):c.305G>A (p.Ser102Asn) rs796053413
NM_001083962.2(TCF4):c.369+1672A>G
NM_001083962.2(TCF4):c.520C>A (p.Arg174=) rs878853149
NM_001083962.2(TCF4):c.550-22814A>G
NM_001083962.2(TCF4):c.576C>A (p.Ala192=) rs143993583
NM_001083962.2(TCF4):c.576C>T (p.Ala192=) rs143993583
NM_001083962.2(TCF4):c.789+327T>G rs184992628
NM_001083962.2(TCF4):c.8A>G (p.His3Arg) rs2097656766
NM_001243226.3(TCF4):c.102A>G (p.Glu34=)
NM_001243226.3(TCF4):c.114A>G (p.Ser38=)
NM_001243226.3(TCF4):c.258C>G (p.Thr86=)

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