ClinVar Miner

List of variants in gene CARD11 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_032415.7(CARD11):c.1630A>C (p.Ile544Leu) rs147687933 0.00276
NM_032415.7(CARD11):c.2301C>T (p.Asp767=) rs144358235 0.00143
NM_032415.7(CARD11):c.3025G>A (p.Val1009Ile) rs147381531 0.00138
NM_032415.7(CARD11):c.3059C>T (p.Thr1020Met) rs116583746 0.00102
NM_032415.7(CARD11):c.3145-3C>T rs200456391 0.00077
NM_032415.7(CARD11):c.2270-4G>A rs371703131 0.00067
NM_032415.7(CARD11):c.3090C>T (p.Asn1030=) rs112241277 0.00065
NM_032415.7(CARD11):c.2670G>A (p.Ser890=) rs146545469 0.00061
NM_032415.7(CARD11):c.2451G>A (p.Ala817=) rs141131560 0.00053
NM_032415.7(CARD11):c.572A>G (p.Asn191Ser) rs147264763 0.00051
NM_032415.7(CARD11):c.805C>T (p.Leu269=) rs201721416 0.00038
NM_032415.7(CARD11):c.3063G>C (p.Glu1021Asp) rs375727923 0.00031
NM_032415.7(CARD11):c.3060G>A (p.Thr1020=) rs138682139 0.00029
NM_032415.7(CARD11):c.2920C>T (p.Arg974Cys) rs201847585 0.00028
NM_032415.7(CARD11):c.1595C>T (p.Thr532Met) rs201780608 0.00021
NM_032415.7(CARD11):c.3139G>A (p.Ala1047Thr) rs146334064 0.00020
NM_032415.7(CARD11):c.1519-7C>T rs370431421 0.00011
NM_032415.7(CARD11):c.2542C>T (p.Arg848Cys) rs753952757 0.00006
NM_032415.7(CARD11):c.1485G>A (p.Pro495=) rs375570275 0.00005
NM_032415.7(CARD11):c.2275C>T (p.Arg759Trp) rs369433934 0.00004
NM_032415.7(CARD11):c.3175G>A (p.Gly1059Ser) rs376446854 0.00004
NM_032415.7(CARD11):c.2269+3G>A rs779109505 0.00003
NM_032415.7(CARD11):c.522A>G (p.Leu174=) rs763041691 0.00003
NM_032415.7(CARD11):c.3144+8G>A rs765942781 0.00002
NM_032415.7(CARD11):c.925C>T (p.Arg309Cys) rs370704955 0.00002
NM_032415.7(CARD11):c.1342-4C>T rs1413809242 0.00001
NM_032415.7(CARD11):c.1462A>C (p.Lys488Gln) rs765683724 0.00001
NM_032415.7(CARD11):c.1782C>T (p.Gly594=) rs1463082614 0.00001
NM_032415.7(CARD11):c.2718C>T (p.Ser906=) rs916415454 0.00001
NM_032415.7(CARD11):c.128C>T (p.Thr43Met) rs2115094112
NM_032415.7(CARD11):c.1316C>T (p.Ser439Phe) rs760856731
NM_032415.7(CARD11):c.1693G>A (p.Ala565Thr)
NM_032415.7(CARD11):c.2179C>T (p.Pro727Ser)
NM_032415.7(CARD11):c.2233G>A (p.Gly745Ser) rs895009948
NM_032415.7(CARD11):c.2243C>T (p.Thr748Met)
NM_032415.7(CARD11):c.239T>C (p.Leu80Pro) rs1780440992
NM_032415.7(CARD11):c.2497C>T (p.Pro833Ser) rs1779483440
NM_032415.7(CARD11):c.268G>T (p.Val90Phe) rs2115090528
NM_032415.7(CARD11):c.2716T>C (p.Ser906Pro)
NM_032415.7(CARD11):c.2721G>A (p.Glu907=)
NM_032415.7(CARD11):c.294T>C (p.Tyr98=)
NM_032415.7(CARD11):c.3077C>G (p.Ser1026Cys)
NM_032415.7(CARD11):c.367G>A (p.Gly123Ser) rs387907352
NM_032415.7(CARD11):c.388T>A (p.Phe130Ile) rs1554276147
NM_032415.7(CARD11):c.442C>A (p.Gln148Lys)
NM_032415.7(CARD11):c.458T>C (p.Leu153Pro) rs2115086780
NM_032415.7(CARD11):c.919C>T (p.His307Tyr) rs2115072662
NM_032415.7(CARD11):c.91C>T (p.His31Tyr) rs1562496455

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