ClinVar Miner

List of variants in gene TCF4 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.789+23C>T rs1788027 0.53241
NM_001083962.2(TCF4):c.1941A>G (p.Ser647=) rs8766 0.37317
NM_001083962.2(TCF4):c.305-165C>T rs17522826 0.15868
NM_001083962.2(TCF4):c.1905G>A (p.Ala635=) rs151150677 0.00274
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.504A>G (p.Val168=) rs370160994 0.00037
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.208-8A>G rs184943897 0.00015
NM_001083962.2(TCF4):c.1113G>A (p.Ser371=) rs148308964 0.00003
NM_001083962.2(TCF4):c.*4+30C>T rs587784457 0.00001
NM_001083962.2(TCF4):c.1185T>C (p.Asp395=) rs1341306301 0.00001
NM_001083962.2(TCF4):c.420G>A (p.Ser140=) rs763742755 0.00001
NM_001083962.2(TCF4):c.1059A>G (p.Pro353=) rs1298461061
NM_001083962.2(TCF4):c.1146+1G>A rs587784458
NM_001083962.2(TCF4):c.1153C>T (p.Arg385Ter) rs121909122
NM_001083962.2(TCF4):c.1165C>T (p.Arg389Cys) rs2145503179
NM_001083962.2(TCF4):c.1299G>A (p.Leu433=) rs552340151
NM_001083962.2(TCF4):c.1350G>A (p.Met450Ile) rs11660217
NM_001083962.2(TCF4):c.1411C>T (p.Gln471Ter) rs797046033
NM_001083962.2(TCF4):c.1498G>T (p.Gly500Ter) rs587784459
NM_001083962.2(TCF4):c.1663G>T (p.Glu555Ter) rs1555711142
NM_001083962.2(TCF4):c.1733G>C (p.Arg578Pro) rs121909123
NM_001083962.2(TCF4):c.1739G>A (p.Arg580Gln) rs121909121
NM_001083962.2(TCF4):c.1741G>T (p.Val581Phe) rs587784460
NM_001083962.2(TCF4):c.1760C>T (p.Ala587Val) rs1555710523
NM_001083962.2(TCF4):c.1777_1779del (p.Arg593del) rs587784461
NM_001083962.2(TCF4):c.1834del (p.His612fs) rs1555710069
NM_001083962.2(TCF4):c.1840G>C (p.Ala614Pro) rs587784462
NM_001083962.2(TCF4):c.1871A>C (p.Gln624Pro) rs797046034
NM_001083962.2(TCF4):c.1965dup (p.Gly656fs) rs797046035
NM_001083962.2(TCF4):c.223A>G (p.Thr75Ala) rs567398278
NM_001083962.2(TCF4):c.415del (p.Leu139fs) rs587784463
NM_001083962.2(TCF4):c.469C>T (p.Arg157Ter) rs587784464
NM_001083962.2(TCF4):c.576C>T (p.Ala192=) rs143993583
NM_001083962.2(TCF4):c.642C>T (p.Ser214=) rs982483524
NM_001083962.2(TCF4):c.649A>C (p.Met217Leu) rs768573052
NM_001083962.2(TCF4):c.652C>T (p.Gln218Ter) rs1064796853
NM_001083962.2(TCF4):c.655+1G>A rs587784465
NM_001083962.2(TCF4):c.655+1_655+2dup rs797046036
NM_001083962.2(TCF4):c.656-1G>C rs587784466
NM_001083962.2(TCF4):c.656-3C>T rs587784467
NM_001083962.2(TCF4):c.726G>A (p.Leu242=) rs765833827
NM_001083962.2(TCF4):c.759C>G (p.Ser253Arg) rs1555796785
NM_001083962.2(TCF4):c.990G>A (p.Ser330=) rs587784469
NM_001083962.2(TCF4):c.991-2A>G rs587784470

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.