ClinVar Miner

List of variants in gene CARD11 studied for not specified

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_032415.7(CARD11):c.2839+70A>G rs1182157 0.99321
NM_032415.7(CARD11):c.2142+13C>T rs2527509 0.62838
NM_032415.7(CARD11):c.3276A>G (p.Arg1092=) rs1124581 0.54386
NM_032415.7(CARD11):c.2622A>G (p.Pro874=) rs3735124 0.32756
NM_032415.7(CARD11):c.1654-29C>T rs2527506 0.23485
NM_032415.7(CARD11):c.1599C>T (p.Asp533=) rs1621509 0.17254
NM_032415.7(CARD11):c.2703+6G>T rs3735123 0.10803
NM_032415.7(CARD11):c.2344C>T (p.Leu782=) rs3735126 0.10660
NM_032415.7(CARD11):c.1808-12G>A rs41469246 0.09723
NM_032415.7(CARD11):c.1755-20del rs145380018 0.09705
NM_032415.7(CARD11):c.3126T>C (p.Ile1042=) rs2301921 0.06205
NM_032415.7(CARD11):c.1590A>C (p.Glu530Asp) rs41515445 0.02483
NM_032415.7(CARD11):c.1923G>A (p.Arg641=) rs41405944 0.00786
NM_032415.7(CARD11):c.1212G>A (p.Arg404=) rs142108678 0.00562
NM_032415.7(CARD11):c.3019+6C>T rs199705831 0.00408
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.1610G>C (p.Ser537Thr) rs148753096 0.00226
NM_032415.7(CARD11):c.3454G>A (p.Asp1152Asn) rs147422861 0.00217
NM_032415.7(CARD11):c.1581C>A (p.His527Gln) rs74876622 0.00182
NM_032415.7(CARD11):c.3019+9C>T rs200741645 0.00152
NM_032415.7(CARD11):c.1812C>T (p.Asp604=) rs149270244 0.00148
NM_032415.7(CARD11):c.3025G>A (p.Val1009Ile) rs147381531 0.00138
NM_032415.7(CARD11):c.1262T>C (p.Met421Thr) rs372864426 0.00113
NM_032415.7(CARD11):c.3059C>T (p.Thr1020Met) rs116583746 0.00102
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.945C>T (p.Asp315=) rs149430714 0.00076
NM_032415.7(CARD11):c.3090C>T (p.Asn1030=) rs112241277 0.00065
NM_032415.7(CARD11):c.1975G>A (p.Val659Met) rs78443994 0.00063
NM_032415.7(CARD11):c.2641A>G (p.Ser881Gly) rs140097633 0.00063
NM_032415.7(CARD11):c.1741G>A (p.Ala581Thr) rs75403455 0.00056
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.2119C>T (p.Arg707Cys) rs143049136 0.00039
NM_032415.7(CARD11):c.3145-14C>T rs201827805 0.00037
NM_032415.7(CARD11):c.2276G>A (p.Arg759Gln) rs148354898 0.00026
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.2921G>A (p.Arg974His) rs750407488 0.00011
NM_032415.7(CARD11):c.2597G>A (p.Arg866Gln) rs150990488 0.00006
NM_032415.7(CARD11):c.1485G>A (p.Pro495=) rs375570275 0.00005
NM_032415.7(CARD11):c.2578G>A (p.Gly860Ser) rs368181734 0.00005
NM_032415.7(CARD11):c.583G>C (p.Val195Leu) rs747351557 0.00004
NM_032415.7(CARD11):c.704G>A (p.Arg235Gln) rs148083162 0.00004
NM_032415.7(CARD11):c.2120G>A (p.Arg707His) rs201948130 0.00002
NM_032415.7(CARD11):c.1823G>A (p.Arg608His) rs587778150 0.00001
NM_032415.7(CARD11):c.2074G>A (p.Val692Met) rs587778151 0.00001
NM_032415.7(CARD11):c.1018-66A>G
NM_032415.7(CARD11):c.1245C>T (p.Asp415=) rs6945582
NM_032415.7(CARD11):c.1535C>G (p.Ser512Cys) rs1562488034
NM_032415.7(CARD11):c.1570+97T>C
NM_032415.7(CARD11):c.1654-27G>A
NM_032415.7(CARD11):c.1755-20A>C rs1182136
NM_032415.7(CARD11):c.1755-26T>C
NM_032415.7(CARD11):c.2242A>G (p.Thr748Ala) rs376122142
NM_032415.7(CARD11):c.2244G>C (p.Thr748=) rs3735131
NM_032415.7(CARD11):c.2269+27C>T
NM_032415.7(CARD11):c.2298G>T (p.Glu766Asp) rs534947493
NM_032415.7(CARD11):c.2395G>A (p.Asp799Asn) rs587778152
NM_032415.7(CARD11):c.2511-77G>A
NM_032415.7(CARD11):c.2704-91G>A
NM_032415.7(CARD11):c.3019+35G>A
NM_032415.7(CARD11):c.3064A>G (p.Thr1022Ala) rs2115026653
NM_032415.7(CARD11):c.3144+156G>C
NM_032415.7(CARD11):c.3261-76G>T
NM_032415.7(CARD11):c.590T>C (p.Val197Ala) rs587778153

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