ClinVar Miner

List of variants in gene TCF4 reported as pathogenic for not provided

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 18q21.2(chr18:52956790-53108471)x1
GRCh37/hg19 18q21.2(chr18:53011022-53131802)x1
NM_001083962.2(TCF4):c.1031del (p.Asn344fs) rs886041910
NM_001083962.2(TCF4):c.1037C>G (p.Ser346Ter) rs1057518339
NM_001083962.2(TCF4):c.1069+1G>A rs797045072
NM_001083962.2(TCF4):c.1086G>A (p.Trp362Ter) rs398123560
NM_001083962.2(TCF4):c.1135_1136insGT (p.Leu379fs) rs1600404016
NM_001083962.2(TCF4):c.1139del (p.His380fs) rs2057097206
NM_001083962.2(TCF4):c.1144_1145del (p.Leu382fs)
NM_001083962.2(TCF4):c.1153C>T (p.Arg385Ter) rs121909122
NM_001083962.2(TCF4):c.1229_1232dup (p.Met411fs) rs2056308423
NM_001083962.2(TCF4):c.1239dup (p.Gly414fs) rs1555764460
NM_001083962.2(TCF4):c.1244del (p.His415fs) rs1600290109
NM_001083962.2(TCF4):c.1295_1296del (p.Gly432fs) rs2056279996
NM_001083962.2(TCF4):c.1304C>A (p.Ser435Ter)
NM_001083962.2(TCF4):c.1414del (p.Val472fs) rs727504174
NM_001083962.2(TCF4):c.1471C>T (p.Gln491Ter) rs886041578
NM_001083962.2(TCF4):c.1505_1518del (p.Gln502fs) rs796053427
NM_001083962.2(TCF4):c.1570C>T (p.Gln524Ter) rs796053418
NM_001083962.2(TCF4):c.1650-2A>G rs1555711245
NM_001083962.2(TCF4):c.1663G>T (p.Glu555Ter) rs1555711142
NM_001083962.2(TCF4):c.1711del (p.Met571fs) rs1555710866
NM_001083962.2(TCF4):c.1726C>T (p.Arg576Ter) rs1555710726
NM_001083962.2(TCF4):c.1727G>A (p.Arg576Gln) rs1057521070
NM_001083962.2(TCF4):c.1732C>T (p.Arg578Cys) rs2144406630
NM_001083962.2(TCF4):c.1733G>A (p.Arg578His) rs121909123
NM_001083962.2(TCF4):c.1738C>T (p.Arg580Trp) rs121909120
NM_001083962.2(TCF4):c.1739G>A (p.Arg580Gln) rs121909121
NM_001083962.2(TCF4):c.1831C>G (p.Leu611Val) rs1555710107
NM_001083962.2(TCF4):c.1832T>C (p.Leu611Pro)
NM_001083962.2(TCF4):c.1841C>T (p.Ala614Val) rs1568303352
NM_001083962.2(TCF4):c.1849G>A (p.Val617Ile) rs1568303086
NM_001083962.2(TCF4):c.1876C>T (p.Arg626Ter) rs1131691735
NM_001083962.2(TCF4):c.1879+1G>T
NM_001083962.2(TCF4):c.1899dup (p.Ala634fs) rs2046922813
NM_001083962.2(TCF4):c.1966_1969dup (p.Pro657fs) rs796053428
NM_001083962.2(TCF4):c.304+1G>A
NM_001083962.2(TCF4):c.469C>T (p.Arg157Ter) rs587784464
NM_001083962.2(TCF4):c.469del (p.Arg157fs) rs1569138023
NM_001083962.2(TCF4):c.514_517del (p.Lys172fs) rs398123561
NM_001083962.2(TCF4):c.516_517dup (p.Val173fs) rs796053424
NM_001083962.2(TCF4):c.520C>T (p.Arg174Ter) rs878853149
NM_001083962.2(TCF4):c.526del (p.Val176fs) rs2082085635
NM_001083962.2(TCF4):c.548C>G (p.Ser183Ter) rs2082083331
NM_001083962.2(TCF4):c.550-2A>C
NM_001083962.2(TCF4):c.652C>T (p.Gln218Ter) rs1064796853
NM_001083962.2(TCF4):c.655+1G>T rs587784465
NM_001083962.2(TCF4):c.655+2T>G
NM_001083962.2(TCF4):c.655G>A (p.Asp219Asn) rs886041248
NM_001083962.2(TCF4):c.665dup (p.His222fs) rs2061391242
NM_001083962.2(TCF4):c.680_682delinsT (p.Trp227fs) rs796053425
NM_001083962.2(TCF4):c.748C>T (p.Gln250Ter) rs727504175
NM_001083962.2(TCF4):c.986_990+3del rs1131691653
NM_001083962.2(TCF4):c.990G>A (p.Ser330=) rs587784469

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