ClinVar Miner

List of variants in gene TCF4 reported as likely benign for not specified

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Gene type:
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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.789+23C>T rs1788027 0.53241
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.305-14G>A rs187703131 0.00084
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.504A>G (p.Val168=) rs370160994 0.00037
NM_001083962.2(TCF4):c.330A>C (p.Ser110=) rs780528611 0.00016
NM_001083962.2(TCF4):c.146-11C>G rs191464553 0.00011
NM_001083962.2(TCF4):c.923-17G>T rs550597992 0.00010
NM_001083962.2(TCF4):c.1147-17C>A rs375777217 0.00009
NM_001083962.2(TCF4):c.1245T>C (p.His415=) rs148909575 0.00006
NM_001083962.2(TCF4):c.207+16C>G rs372770124 0.00006
NM_001083962.2(TCF4):c.-21+12C>T rs1055665608 0.00004
NM_001083962.2(TCF4):c.-29G>A rs796053410 0.00004
NM_001083962.2(TCF4):c.216A>C (p.Gly72=) rs373658921 0.00004
NM_001083962.2(TCF4):c.594G>A (p.Ser198=) rs368553922 0.00004
NM_001083962.2(TCF4):c.945C>T (p.Ala315=) rs200115299 0.00004
NM_001083962.2(TCF4):c.1113G>A (p.Ser371=) rs148308964 0.00003
NM_001083962.2(TCF4):c.1486+4G>C rs201274415 0.00003
NM_001083962.2(TCF4):c.1773C>T (p.Leu591=) rs761419131 0.00002
NM_001083962.2(TCF4):c.*4+30C>T rs587784457 0.00001
NM_001083962.2(TCF4):c.*5-18T>C rs1057520383 0.00001
NM_001083962.2(TCF4):c.-21+18C>T rs1248173869 0.00001
NM_001083962.2(TCF4):c.1185T>C (p.Asp395=) rs1341306301 0.00001
NM_001083962.2(TCF4):c.1587G>A (p.Ser529=) rs567457339 0.00001
NM_001083962.2(TCF4):c.1879+13C>T rs1057524324 0.00001
NM_001083962.2(TCF4):c.305-15C>T rs771654348 0.00001
NM_001083962.2(TCF4):c.500-18A>G rs751585776 0.00001
NM_001083962.2(TCF4):c.687C>A (p.Ser229=) rs200800656 0.00001
NM_001083962.2(TCF4):c.726G>T (p.Leu242Phe) rs765833827 0.00001
NM_001083962.2(TCF4):c.-21+20G>A rs1555785143
NM_001083962.2(TCF4):c.1059A>G (p.Pro353=) rs1298461061
NM_001083962.2(TCF4):c.1062T>C (p.Ser354=)
NM_001083962.2(TCF4):c.1308G>A (p.Gly436=) rs1057523618
NM_001083962.2(TCF4):c.1316C>T (p.Thr439Ile) rs778753474
NM_001083962.2(TCF4):c.1650-18A>T rs1555711333
NM_001083962.2(TCF4):c.1848C>T (p.Ala616=) rs759645955
NM_001083962.2(TCF4):c.1887T>C (p.Asn629=) rs1188688924
NM_001083962.2(TCF4):c.1990G>A (p.Ala664Thr) rs755332116
NM_001083962.2(TCF4):c.223A>G (p.Thr75Ala) rs567398278
NM_001083962.2(TCF4):c.369+12T>G rs777983584
NM_001083962.2(TCF4):c.413C>G (p.Thr138Ser) rs796053416
NM_001083962.2(TCF4):c.499+12C>G
NM_001083962.2(TCF4):c.576C>T (p.Ala192=) rs143993583
NM_001083962.2(TCF4):c.594G>T (p.Ser198=) rs368553922
NM_001083962.2(TCF4):c.656-3C>T rs587784467
NM_001083962.2(TCF4):c.990+13dup rs1555777935

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