ClinVar Miner

List of variants in gene CARD11 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_032415.7(CARD11):c.2119C>T (p.Arg707Cys) rs143049136 0.00039
NM_032415.7(CARD11):c.2920C>T (p.Arg974Cys) rs201847585 0.00028
NM_032415.7(CARD11):c.2735G>A (p.Arg912Gln) rs368119340 0.00015
NM_032415.7(CARD11):c.2239G>A (p.Val747Ile) rs769577430 0.00006
NM_032415.7(CARD11):c.2899C>T (p.Arg967Cys) rs149857605 0.00006
NM_032415.7(CARD11):c.3382G>A (p.Val1128Ile) rs372251654 0.00004
NM_032415.7(CARD11):c.2063G>A (p.Arg688Gln) rs764342695 0.00001

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