ClinVar Miner

List of variants in gene TCF4 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.1941A>G (p.Ser647=) rs8766 0.37317
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.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.341G>A (p.Arg114Lys) rs139876825 0.00043
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.330A>C (p.Ser110=) rs780528611 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.1245T>C (p.His415=) rs148909575 0.00006
NM_001083962.2(TCF4):c.1704G>A (p.Glu568=) rs144068462 0.00006
NM_001083962.2(TCF4):c.1283G>T (p.Gly428Val) rs186508321 0.00004
NM_001083962.2(TCF4):c.660C>T (p.Gly220=) rs149861305 0.00004
NM_001083962.2(TCF4):c.1486+4G>C rs201274415 0.00003
NM_001083962.2(TCF4):c.1608C>T (p.Asp536=) rs370405835 0.00003
NM_001083962.2(TCF4):c.466C>A (p.Pro156Thr) rs200889338 0.00003
NM_001083962.2(TCF4):c.1032C>T (p.Asn344=) rs372738049 0.00001
NM_001083962.2(TCF4):c.1349T>C (p.Met450Thr) rs774283982 0.00001
NM_001083962.2(TCF4):c.1412A>G (p.Gln471Arg) rs1285770614 0.00001
NM_001083962.2(TCF4):c.1598A>G (p.Lys533Arg) rs1568329915 0.00001
NM_001083962.2(TCF4):c.639C>T (p.Ser213=) rs771829952 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.1056T>C (p.Pro352=)
NM_001083962.2(TCF4):c.1061C>G (p.Ser354Cys)
NM_001083962.2(TCF4):c.1070-2A>G
NM_001083962.2(TCF4):c.107G>C (p.Gly36Ala)
NM_001083962.2(TCF4):c.1142_1143del (p.Ser381fs)
NM_001083962.2(TCF4):c.1180G>C (p.Asp394His) rs1198693569
NM_001083962.2(TCF4):c.119T>C (p.Leu40Ser)
NM_001083962.2(TCF4):c.1267_1268del (p.Gly423fs) rs1555764170
NM_001083962.2(TCF4):c.1299G>A (p.Leu433=) rs552340151
NM_001083962.2(TCF4):c.1304C>G (p.Ser435Ter) rs1555763998
NM_001083962.2(TCF4):c.1399_1403del (p.Leu467fs)
NM_001083962.2(TCF4):c.1486+2T>C rs1555721921
NM_001083962.2(TCF4):c.1518CTC[1] (p.Ser508del)
NM_001083962.2(TCF4):c.1628C>T (p.Ser543Leu)
NM_001083962.2(TCF4):c.1683G>A (p.Gln561=) rs71368997
NM_001083962.2(TCF4):c.1720A>G (p.Asn574Asp) rs2047119736
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.1733G>A (p.Arg578His) rs121909123
NM_001083962.2(TCF4):c.1738C>T (p.Arg580Trp) rs121909120
NM_001083962.2(TCF4):c.1772_1776delinsCT (p.Leu591_Gly592delinsPro) rs1555710416
NM_001083962.2(TCF4):c.1811_1822del (p.Pro604_Lys607del) rs1555710171
NM_001083962.2(TCF4):c.1816A>C (p.Thr606Pro) rs2047096127
NM_001083962.2(TCF4):c.1876C>T (p.Arg626Ter) rs1131691735
NM_001083962.2(TCF4):c.1942G>C (p.Glu648Gln)
NM_001083962.2(TCF4):c.2003T>G (p.Met668Arg)
NM_001083962.2(TCF4):c.223A>G (p.Thr75Ala) rs567398278
NM_001083962.2(TCF4):c.242C>G (p.Thr81Ser)
NM_001083962.2(TCF4):c.387T>C (p.Gly129=)
NM_001083962.2(TCF4):c.413C>G (p.Thr138Ser) rs796053416
NM_001083962.2(TCF4):c.421C>T (p.Pro141Ser) rs2144786748
NM_001083962.2(TCF4):c.450G>A (p.Gln150=)
NM_001083962.2(TCF4):c.469del (p.Arg157fs) rs1569138023
NM_001083962.2(TCF4):c.569G>A (p.Ser190Asn)
NM_001083962.2(TCF4):c.579C>G (p.Asp193Glu)
NM_001083962.2(TCF4):c.624del (p.Ser209fs) rs2062118353
NM_001083962.2(TCF4):c.673del (p.Asp225fs) rs1555797248
NM_001083962.2(TCF4):c.680G>A (p.Trp227Ter) rs1555797231
NM_001083962.2(TCF4):c.692G>A (p.Ser231Asn)
NM_001083962.2(TCF4):c.82C>T (p.Pro28Ser)
NM_001083962.2(TCF4):c.931G>T (p.Gly311Ter) rs1555778204
NM_001083962.2(TCF4):c.991-1G>A

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