ClinVar Miner

List of variants in gene CARD11 reported as likely benign for not specified

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_032415.7(CARD11):c.2913C>T (p.Cys971=) rs61757651 0.00328
NM_032415.7(CARD11):c.1630A>C (p.Ile544Leu) rs147687933 0.00276
NM_032415.7(CARD11):c.3144+9G>A rs112606562 0.00264
NM_032415.7(CARD11):c.519G>A (p.Leu173=) rs41473147 0.00260
NM_032415.7(CARD11):c.1812C>T (p.Asp604=) rs149270244 0.00148
NM_032415.7(CARD11):c.180G>T (p.Val60=) rs117016854 0.00091
NM_032415.7(CARD11):c.2060C>T (p.Ala687Val) rs41493047 0.00088
NM_032415.7(CARD11):c.3145-3C>T rs200456391 0.00077
NM_032415.7(CARD11):c.3090C>T (p.Asn1030=) rs112241277 0.00065
NM_032415.7(CARD11):c.2451G>A (p.Ala817=) rs141131560 0.00053
NM_032415.7(CARD11):c.3145-14C>T rs201827805 0.00037
NM_032415.7(CARD11):c.1595C>T (p.Thr532Met) rs201780608 0.00021
NM_032415.7(CARD11):c.1485G>A (p.Pro495=) rs375570275 0.00005
NM_032415.7(CARD11):c.2578G>A (p.Gly860Ser) rs368181734 0.00005

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