ClinVar Miner

List of variants in gene TCF4 reported as uncertain significance for not provided

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Gene type:
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Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.341G>A (p.Arg114Lys) rs139876825 0.00043
NM_001083962.2(TCF4):c.504A>G (p.Val168=) rs370160994 0.00037
NM_001083962.2(TCF4):c.1245T>C (p.His415=) rs148909575 0.00006
NM_001083962.2(TCF4):c.991-6T>G rs201721676 0.00005
NM_001083962.2(TCF4):c.1283G>T (p.Gly428Val) rs186508321 0.00004
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_001083962.2(TCF4):c.550-22803C>T rs891060887 0.00002
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.573T>C (p.Thr191=) rs1434749460 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.946G>A (p.Gly316Ser) rs993457884 0.00001
NM_001243230.2(TCF4):c.13A>G (p.Lys5Glu) rs1373298140 0.00001
GRCh37/hg19 18q21.2(chr18:52640139-53090100)x3
GRCh37/hg19 18q21.2(chr18:53144168-53366573)x3
NM_001083962.2(TCF4):c.*1A>G rs794727223
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.1057C>A (p.Pro353Thr)
NM_001083962.2(TCF4):c.1145T>C (p.Leu382Ser)
NM_001083962.2(TCF4):c.1196T>C (p.Val399Ala) rs2145502188
NM_001083962.2(TCF4):c.1207_1208delinsAT (p.His403Ile)
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.146-46442G>T rs1164726138
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.1774G>A (p.Gly592Ser) rs751190049
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.2000A>G (p.His667Arg) rs1555707461
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.305-102G>A
NM_001083962.2(TCF4):c.322T>G (p.Ser108Ala) rs112222111
NM_001083962.2(TCF4):c.337G>T (p.Gly113Trp) rs1556050492
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.549+28682G>A
NM_001083962.2(TCF4):c.577G>A (p.Asp193Asn) rs1044163650
NM_001083962.2(TCF4):c.594G>T (p.Ser198=) rs368553922
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.655+54C>T
NM_001083962.2(TCF4):c.699G>C (p.Met233Ile) rs1233945994
NM_001083962.2(TCF4):c.715G>C (p.Ala239Pro) rs747361615
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.959C>T (p.Thr320Ile)
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
NM_001243226.3(TCF4):c.187C>T (p.Pro63Ser)
NM_001243226.3(TCF4):c.59T>G (p.Phe20Cys) rs2148012111
NM_001243226.3(TCF4):c.74del (p.Asn25fs) rs752700752
NM_003199.2(TCF4):c.-458A>C rs1603624952

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