ClinVar Miner

List of variants in gene CARD11 reported as benign by Invitae

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
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.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.1440G>A (p.Ser480=) rs41396348 0.06979
NM_032415.7(CARD11):c.3126T>C (p.Ile1042=) rs2301921 0.06205
NM_032415.7(CARD11):c.225G>C (p.Arg75=) rs10229368 0.05950
NM_032415.7(CARD11):c.2748C>T (p.Asn916=) rs61731201 0.03467
NM_032415.7(CARD11):c.1590A>C (p.Glu530Asp) rs41515445 0.02483
NM_032415.7(CARD11):c.1695C>T (p.Ala565=) rs41454944 0.02103
NM_032415.7(CARD11):c.220+16C>T rs41400946 0.01297
NM_032415.7(CARD11):c.1923G>A (p.Arg641=) rs41405944 0.00786
NM_032415.7(CARD11):c.1260G>A (p.Glu420=) rs112171353 0.00738
NM_032415.7(CARD11):c.1212G>A (p.Arg404=) rs142108678 0.00562
NM_032415.7(CARD11):c.1755-17del rs376854528 0.00423
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.3144+9G>A rs112606562 0.00264
NM_032415.7(CARD11):c.519G>A (p.Leu173=) rs41473147 0.00260
NM_032415.7(CARD11):c.3019+7G>A rs184926618 0.00165
NM_032415.7(CARD11):c.1143+12A>C rs201831026 0.00154
NM_032415.7(CARD11):c.2142+14G>A rs113985724 0.00152
NM_032415.7(CARD11):c.3019+9C>T rs200741645 0.00152
NM_032415.7(CARD11):c.1227G>A (p.Glu409=) rs115457946 0.00150
NM_032415.7(CARD11):c.1812C>T (p.Asp604=) rs149270244 0.00148
NM_032415.7(CARD11):c.2301C>T (p.Asp767=) rs144358235 0.00143
NM_032415.7(CARD11):c.3399C>T (p.Arg1133=) rs117428786 0.00138
NM_032415.7(CARD11):c.358+17T>C rs41385747 0.00116
NM_032415.7(CARD11):c.3396C>T (p.Leu1132=) rs140481165 0.00102
NM_032415.7(CARD11):c.2061G>A (p.Ala687=) rs145745268 0.00098
NM_032415.7(CARD11):c.180G>T (p.Val60=) rs117016854 0.00091
NM_032415.7(CARD11):c.2367C>T (p.Asp789=) rs41349451 0.00091
NM_032415.7(CARD11):c.3090C>T (p.Asn1030=) rs112241277 0.00065
NM_032415.7(CARD11):c.2641A>G (p.Ser881Gly) rs140097633 0.00063
NM_032415.7(CARD11):c.2670G>A (p.Ser890=) rs146545469 0.00061
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.805C>T (p.Leu269=) rs201721416 0.00038
NM_032415.7(CARD11):c.2499C>T (p.Pro833=) rs150171618 0.00019
NM_032415.7(CARD11):c.1017+20G>A rs111763425 0.00015
NM_032415.7(CARD11):c.2735G>A (p.Arg912Gln) rs368119340 0.00015
NM_032415.7(CARD11):c.3113C>T (p.Ala1038Val) rs374682435 0.00011
NM_032415.7(CARD11):c.2900G>A (p.Arg967His) rs141751925 0.00004
NM_032415.7(CARD11):c.1582G>A (p.Glu528Lys) rs367917190 0.00001
NM_032415.7(CARD11):c.1245C>T (p.Asp415=) rs6945582
NM_032415.7(CARD11):c.1581C>T (p.His527=)
NM_032415.7(CARD11):c.159T>C (p.Asp53=)
NM_032415.7(CARD11):c.1600G>A (p.Ala534Thr)
NM_032415.7(CARD11):c.1755-20A>C rs1182136
NM_032415.7(CARD11):c.1882C>T (p.Leu628=)
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.3019+17G>A rs181294101
NM_032415.7(CARD11):c.60C>T (p.Asp20=)

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