ClinVar Miner

List of variants in gene TCF4 studied for not specified

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Gene type:
ClinVar version:
Total variants: 82
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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.73-3T>C rs148658897 0.00182
NM_001083962.2(TCF4):c.1419G>C (p.Pro473=) rs143944746 0.00178
NM_001083962.2(TCF4):c.*22G>A rs182372608 0.00139
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.944C>T (p.Ala315Val) rs147445499 0.00066
NM_001083962.2(TCF4):c.*5-10C>T rs552239655 0.00052
NM_001083962.2(TCF4):c.1577C>T (p.Thr526Met) rs202025804 0.00051
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.207+13A>G rs200824801 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.1551C>T (p.Asp517=) rs140862252 0.00012
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.1704G>A (p.Glu568=) rs144068462 0.00006
NM_001083962.2(TCF4):c.207+16C>G rs372770124 0.00006
NM_001083962.2(TCF4):c.370-14T>C rs796053411 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.1995G>A (p.Ser665=) rs587781188 0.00003
NM_001083962.2(TCF4):c.1650-14C>T rs569480730 0.00002
NM_001083962.2(TCF4):c.1773C>T (p.Leu591=) rs761419131 0.00002
NM_001083962.1(TCF4):c.-511G>A rs1057518280 0.00001
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.1989C>T (p.Asp663=) rs752325141 0.00001
NM_001083962.2(TCF4):c.305-15C>T rs771654348 0.00001
NM_001083962.2(TCF4):c.420G>A (p.Ser140=) rs763742755 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.706C>G (p.Pro236Ala) rs139859596 0.00001
NM_001083962.2(TCF4):c.726G>T (p.Leu242Phe) rs765833827 0.00001
GRCh37/hg19 18q21.2(chr18:52903599-53084300)x1
GRCh37/hg19 18q21.2(chr18:52978878-53100587)x1
GRCh37/hg19 18q21.2(chr18:53089162-53292031)x1
GRCh37/hg19 18q21.2(chr18:53277008-53428347)
GRCh37/hg19 18q21.2(chr18:53289889-53383013)
NM_001083962.2(TCF4):c.-21+20G>A rs1555785143
NM_001083962.2(TCF4):c.-37C>T rs796053409
NM_001083962.2(TCF4):c.1059A>G (p.Pro353=) rs1298461061
NM_001083962.2(TCF4):c.1062T>C (p.Ser354=)
NM_001083962.2(TCF4):c.1147-3C>G rs2056333687
NM_001083962.2(TCF4):c.1299G>A (p.Leu433=) rs552340151
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.642C>T (p.Ser214=) rs982483524
NM_001083962.2(TCF4):c.649A>C (p.Met217Leu) rs768573052
NM_001083962.2(TCF4):c.656-3C>T rs587784467
NM_001083962.2(TCF4):c.72+8_72+11del rs749161770
NM_001083962.2(TCF4):c.726G>A (p.Leu242=) rs765833827
NM_001083962.2(TCF4):c.733TCT[1] (p.Ser246del) rs796053426
NM_001083962.2(TCF4):c.990+13dup rs1555777935

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