ClinVar Miner

List of variants in gene TCF4 reported as uncertain significance by GeneDx

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.991-6T>G rs201721676 0.00005
NM_001083962.2(TCF4):c.1348A>G (p.Met450Val) rs1466719628 0.00002
NM_001083962.2(TCF4):c.245G>A (p.Ser82Asn) rs773462232 0.00002
NM_001083962.1(TCF4):c.-511G>A rs1057518280 0.00001
NM_001083962.2(TCF4):c.1106C>A (p.Ala369Asp) rs1016959427 0.00001
NM_001083962.2(TCF4):c.1307G>C (p.Gly436Ala) rs758564063 0.00001
NM_001083962.2(TCF4):c.1318G>A (p.Gly440Ser) rs759754956 0.00001
NM_001083962.2(TCF4):c.1586C>T (p.Ser529Leu) rs796053419 0.00001
NM_001083962.2(TCF4):c.200C>T (p.Pro67Leu) rs763329139 0.00001
NM_001083962.2(TCF4):c.212A>G (p.Tyr71Cys) rs763349461 0.00001
NM_001083962.2(TCF4):c.446A>G (p.Tyr149Cys) rs1603286090 0.00001
NM_001083962.2(TCF4):c.549A>T (p.Ser183=) rs919002190 0.00001
NM_001083962.2(TCF4):c.593C>T (p.Ser198Leu) rs1313604252 0.00001
NM_001083962.2(TCF4):c.649A>T (p.Met217Leu) rs768573052 0.00001
NM_001083962.2(TCF4):c.706C>G (p.Pro236Ala) rs139859596 0.00001
NM_001083962.2(TCF4):c.*4+1G>A rs2144361580
NM_001083962.2(TCF4):c.*5-1G>A rs796053421
NM_001083962.2(TCF4):c.-21+2T>A rs1568471128
NM_001083962.2(TCF4):c.1007A>G (p.His336Arg)
NM_001083962.2(TCF4):c.1145T>C (p.Leu382Ser)
NM_001083962.2(TCF4):c.124A>G (p.Ser42Gly) rs796053423
NM_001083962.2(TCF4):c.1379C>T (p.Ala460Val) rs2144678680
NM_001083962.2(TCF4):c.1440G>C (p.Gln480His) rs1555722153
NM_001083962.2(TCF4):c.146-6C>T
NM_001083962.2(TCF4):c.1474G>C (p.Asp492His)
NM_001083962.2(TCF4):c.1489A>G (p.Met497Val) rs946579858
NM_001083962.2(TCF4):c.1608C>G (p.Asp536Glu)
NM_001083962.2(TCF4):c.1789C>G (p.Leu597Val)
NM_001083962.2(TCF4):c.1907G>A (p.Cys636Tyr) rs1057524669
NM_001083962.2(TCF4):c.1912A>G (p.Lys638Glu)
NM_001083962.2(TCF4):c.1929G>C (p.Glu643Asp) rs796053412
NM_001083962.2(TCF4):c.235C>G (p.His79Asp) rs957698131
NM_001083962.2(TCF4):c.280C>T (p.Pro94Ser) rs779916094
NM_001083962.2(TCF4):c.322T>G (p.Ser108Ala) rs112222111
NM_001083962.2(TCF4):c.345A>T (p.Glu115Asp)
NM_001083962.2(TCF4):c.368A>G (p.Gln123Arg) rs2146490226
NM_001083962.2(TCF4):c.389A>G (p.Asp130Gly) rs796053414
NM_001083962.2(TCF4):c.404A>G (p.Asn135Ser) rs2144787307
NM_001083962.2(TCF4):c.410G>A (p.Gly137Glu) rs796053415
NM_001083962.2(TCF4):c.421C>T (p.Pro141Ser) rs2144786748
NM_001083962.2(TCF4):c.443A>T (p.Tyr148Phe)
NM_001083962.2(TCF4):c.497T>C (p.Met166Thr)
NM_001083962.2(TCF4):c.498G>A (p.Met166Ile)
NM_001083962.2(TCF4):c.508A>G (p.Thr170Ala) rs796053417
NM_001083962.2(TCF4):c.529C>T (p.Pro177Ser) rs2144766710
NM_001083962.2(TCF4):c.577G>A (p.Asp193Asn) rs1044163650
NM_001083962.2(TCF4):c.635C>G (p.Pro212Arg) rs2146264091
NM_001083962.2(TCF4):c.650T>C (p.Met217Thr) rs2146263735
NM_001083962.2(TCF4):c.733TCT[1] (p.Ser246del) rs796053426
NM_001083962.2(TCF4):c.83C>T (p.Pro28Leu)
NM_001083962.2(TCF4):c.923-11del
NM_001083962.2(TCF4):c.935G>A (p.Ser312Asn)
NM_001083962.2(TCF4):c.979G>C (p.Ala327Pro)
NM_001083962.2(TCF4):c.988T>G (p.Ser330Ala) rs2145729351
NM_001083962.2(TCF4):c.990+3G>T
NM_001083962.2(TCF4):c.991-8_991-4del rs766726309

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