ClinVar Miner

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

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Gene type:
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Total variants: 22
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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.*22G>A rs182372608 0.00139
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.207+13A>G rs200824801 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.1704G>A (p.Glu568=) rs144068462 0.00006
NM_001083962.2(TCF4):c.370-14T>C rs796053411 0.00006
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.-37C>T rs796053409
NM_001083962.2(TCF4):c.1299G>A (p.Leu433=) rs552340151

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