ClinVar Miner

List of variants in gene TCF3 reported as likely benign for agammaglobulinemia

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_003200.5(TCF3):c.1713G>A (p.Glu571=) rs143212973 0.00394
NM_003200.5(TCF3):c.1154G>A (p.Gly385Asp) rs117006898 0.00282
NM_003200.5(TCF3):c.315G>A (p.Arg105=) rs144176765 0.00160
NM_003200.5(TCF3):c.136G>A (p.Gly46Arg) rs143529809 0.00039
NM_003200.5(TCF3):c.1564A>C (p.Lys522Gln) rs201831565 0.00029
NM_003200.5(TCF3):c.823-13C>T rs148835727 0.00019
NM_003200.5(TCF3):c.1948C>A (p.Pro650Thr) rs7252811 0.00013
NM_003200.5(TCF3):c.1806G>A (p.Leu602=) rs1376446279
NM_003200.5(TCF3):c.879CTC[1] (p.Ser295del) rs550914200

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