ClinVar Miner

List of variants in gene CARD8 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 234
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001184900.3(CARD8):c.1324G>C (p.Ala442Pro) rs149691235 0.00049
NM_001184900.3(CARD8):c.1375C>T (p.Arg459Trp) rs150504639 0.00044
NM_001184900.3(CARD8):c.973C>A (p.Pro325Thr) rs139160093 0.00044
NM_001184900.3(CARD8):c.1484G>A (p.Arg495Gln) rs149162452 0.00031
NM_001184900.3(CARD8):c.210G>A (p.Thr70=) rs201361713 0.00029
NM_001184900.3(CARD8):c.3G>A (p.Met1Ile) rs571765227 0.00026
NM_001184900.3(CARD8):c.755A>G (p.His252Arg) rs142485811 0.00017
NM_001184900.3(CARD8):c.352G>C (p.Val118Leu) rs536212135 0.00014
NM_001184900.3(CARD8):c.1483C>T (p.Arg495Trp) rs146657505 0.00011
NM_001184900.3(CARD8):c.58C>T (p.Arg20Trp) rs923351245 0.00010
NM_001184900.3(CARD8):c.1093A>G (p.Met365Val) rs140600610 0.00009
NM_001184900.3(CARD8):c.863A>G (p.Tyr288Cys) rs761116872 0.00008
NM_001184900.3(CARD8):c.1035+5G>A rs117116337 0.00007
NM_001184900.3(CARD8):c.284C>T (p.Thr95Ile) rs188154027 0.00006
NM_001184900.3(CARD8):c.308G>A (p.Arg103His) rs536343060 0.00006
NM_001184900.3(CARD8):c.838C>T (p.His280Tyr) rs141540433 0.00006
NM_001184900.3(CARD8):c.970C>T (p.His324Tyr) rs141307910 0.00006
NM_001184900.3(CARD8):c.1094T>G (p.Met365Arg) rs149003172 0.00004
NM_001184900.3(CARD8):c.307C>T (p.Arg103Cys) rs780214022 0.00004
NM_001184900.3(CARD8):c.599T>C (p.Leu200Pro) rs771578974 0.00004
NM_001184900.3(CARD8):c.815A>G (p.Lys272Arg) rs369099893 0.00004
NM_001184900.3(CARD8):c.1018G>A (p.Asp340Asn) rs774740059 0.00003
NM_001184900.3(CARD8):c.1585G>A (p.Val529Met) rs146880951 0.00003
NM_001184900.3(CARD8):c.543-9T>A rs752981551 0.00003
NM_001184900.3(CARD8):c.826A>C (p.Met276Leu) rs754710410 0.00003
NM_001184900.3(CARD8):c.999del (p.Leu334fs) rs750044997 0.00003
NM_001184900.3(CARD8):c.1149A>G (p.Lys383=) rs758762341 0.00002
NM_001184900.3(CARD8):c.480G>C (p.Gln160His) rs145216351 0.00002
NM_001184900.3(CARD8):c.1021G>A (p.Ala341Thr) rs773369968 0.00001
NM_001184900.3(CARD8):c.1058G>A (p.Arg353His) rs540915752 0.00001
NM_001184900.3(CARD8):c.215A>G (p.Tyr72Cys) rs1310564759 0.00001
NM_001184900.3(CARD8):c.335G>C (p.Gly112Ala) rs1264418977 0.00001
NM_001184900.3(CARD8):c.342C>A (p.Asp114Glu) rs1280184111 0.00001
NM_001184900.3(CARD8):c.382C>T (p.Gln128Ter) rs771293789 0.00001
NM_001184900.3(CARD8):c.491C>G (p.Pro164Arg) rs751433350 0.00001
NM_001184900.3(CARD8):c.536dup (p.Tyr180fs) rs777902590 0.00001
NM_001184900.3(CARD8):c.694G>A (p.Gly232Ser) rs370395701 0.00001
NM_001184900.3(CARD8):c.910C>T (p.Arg304Trp) rs770885397 0.00001
NC_000019.10:g.48234544del
NC_000019.9:g.(?_48714967)_(48725132_?)del
NC_000019.9:g.(?_48714967)_(48737820_?)del
NC_000019.9:g.(?_48724967)_(48725132_?)del
NC_000019.9:g.(?_48744199)_(48744277_?)del
NM_001184900.3(CARD8):c.1002G>T (p.Leu334Phe)
NM_001184900.3(CARD8):c.1002del (p.Leu334fs)
NM_001184900.3(CARD8):c.1009G>A (p.Val337Ile)
NM_001184900.3(CARD8):c.1009G>T (p.Val337Phe)
NM_001184900.3(CARD8):c.1017C>A (p.Ser339Arg) rs760059064
NM_001184900.3(CARD8):c.1036-10_1036-9delinsGT
NM_001184900.3(CARD8):c.1037C>T (p.Ala346Val)
NM_001184900.3(CARD8):c.1040T>C (p.Ile347Thr)
NM_001184900.3(CARD8):c.1047T>A (p.Asp349Glu)
NM_001184900.3(CARD8):c.1048G>A (p.Glu350Lys)
NM_001184900.3(CARD8):c.1057C>G (p.Arg353Gly) rs140937765
NM_001184900.3(CARD8):c.1057C>T (p.Arg353Cys)
NM_001184900.3(CARD8):c.1058G>C (p.Arg353Pro)
NM_001184900.3(CARD8):c.1058G>T (p.Arg353Leu)
NM_001184900.3(CARD8):c.1062C>G (p.Phe354Leu)
NM_001184900.3(CARD8):c.1069G>T (p.Val357Leu)
NM_001184900.3(CARD8):c.1072C>T (p.Arg358Cys)
NM_001184900.3(CARD8):c.1073G>A (p.Arg358His)
NM_001184900.3(CARD8):c.1085C>T (p.Ser362Leu)
NM_001184900.3(CARD8):c.1099C>A (p.Pro367Thr)
NM_001184900.3(CARD8):c.1116del (p.Ser373fs)
NM_001184900.3(CARD8):c.1147_1150del (p.Leu382_Lys383insTer)
NM_001184900.3(CARD8):c.1160A>G (p.Lys387Arg)
NM_001184900.3(CARD8):c.1161+5G>A rs2145766229
NM_001184900.3(CARD8):c.1161G>T (p.Lys387Asn)
NM_001184900.3(CARD8):c.1162-2A>G
NM_001184900.3(CARD8):c.1169A>G (p.Lys390Arg)
NM_001184900.3(CARD8):c.11dup (p.Glu5fs) rs759553123
NM_001184900.3(CARD8):c.1207T>A (p.Ser403Thr)
NM_001184900.3(CARD8):c.1217A>G (p.Tyr406Cys)
NM_001184900.3(CARD8):c.1226A>T (p.Gln409Leu)
NM_001184900.3(CARD8):c.1236A>T (p.Glu412Asp)
NM_001184900.3(CARD8):c.1245A>C (p.Gln415His)
NM_001184900.3(CARD8):c.1245A>T (p.Gln415His) rs1568678740
NM_001184900.3(CARD8):c.1256C>A (p.Thr419Asn)
NM_001184900.3(CARD8):c.1262A>G (p.Lys421Arg)
NM_001184900.3(CARD8):c.1270G>A (p.Gly424Arg)
NM_001184900.3(CARD8):c.1276T>A (p.Leu426Met) rs763961255
NM_001184900.3(CARD8):c.1288A>G (p.Thr430Ala)
NM_001184900.3(CARD8):c.1291G>A (p.Glu431Lys)
NM_001184900.3(CARD8):c.1303+2T>G rs2039924056
NM_001184900.3(CARD8):c.1318G>A (p.Val440Ile)
NM_001184900.3(CARD8):c.1334C>T (p.Pro445Leu)
NM_001184900.3(CARD8):c.1346C>T (p.Ser449Leu)
NM_001184900.3(CARD8):c.1348+2dup
NM_001184900.3(CARD8):c.1349-2A>G
NM_001184900.3(CARD8):c.1349-3C>T
NM_001184900.3(CARD8):c.1349G>T (p.Gly450Val)
NM_001184900.3(CARD8):c.1360G>A (p.Val454Met)
NM_001184900.3(CARD8):c.1368G>C (p.Glu456Asp)
NM_001184900.3(CARD8):c.1376G>A (p.Arg459Gln)
NM_001184900.3(CARD8):c.1417G>A (p.Asp473Asn)
NM_001184900.3(CARD8):c.1423C>T (p.Leu475Phe)
NM_001184900.3(CARD8):c.1431C>G (p.Asp477Glu)
NM_001184900.3(CARD8):c.1438G>C (p.Val480Leu)
NM_001184900.3(CARD8):c.1440_1443dup (p.Thr482fs) rs1269018291
NM_001184900.3(CARD8):c.1456A>G (p.Lys486Glu)
NM_001184900.3(CARD8):c.1459_1460delinsTT (p.Glu487Leu) rs2123789923
NM_001184900.3(CARD8):c.1468G>A (p.Glu490Lys)
NM_001184900.3(CARD8):c.1474G>T (p.Glu492Ter)
NM_001184900.3(CARD8):c.1493A>G (p.Lys498Arg)
NM_001184900.3(CARD8):c.1496A>G (p.Asn499Ser)
NM_001184900.3(CARD8):c.1502C>A (p.Ala501Asp)
NM_001184900.3(CARD8):c.1510A>G (p.Ser504Gly)
NM_001184900.3(CARD8):c.1511G>A (p.Ser504Asn)
NM_001184900.3(CARD8):c.1541T>C (p.Leu514Pro)
NM_001184900.3(CARD8):c.1545C>G (p.Asp515Glu)
NM_001184900.3(CARD8):c.1546G>A (p.Val516Met)
NM_001184900.3(CARD8):c.1556G>T (p.Arg519Ile)
NM_001184900.3(CARD8):c.1592A>G (p.Tyr531Cys)
NM_001184900.3(CARD8):c.17G>A (p.Cys6Tyr)
NM_001184900.3(CARD8):c.216C>G (p.Tyr72Ter)
NM_001184900.3(CARD8):c.220G>A (p.Glu74Lys)
NM_001184900.3(CARD8):c.230G>C (p.Cys77Ser)
NM_001184900.3(CARD8):c.232G>A (p.Val78Ile) rs1372987218
NM_001184900.3(CARD8):c.242C>T (p.Thr81Ile)
NM_001184900.3(CARD8):c.248G>A (p.Cys83Tyr)
NM_001184900.3(CARD8):c.24A>T (p.Glu8Asp) rs2146671147
NM_001184900.3(CARD8):c.256T>G (p.Ser86Ala)
NM_001184900.3(CARD8):c.271G>A (p.Glu91Lys)
NM_001184900.3(CARD8):c.273A>T (p.Glu91Asp)
NM_001184900.3(CARD8):c.273del (p.Asp92fs) rs763265152
NM_001184900.3(CARD8):c.276TGA[1] (p.Asp93del) rs2146365376
NM_001184900.3(CARD8):c.282G>C (p.Glu94Asp)
NM_001184900.3(CARD8):c.287_288del (p.Glu96fs)
NM_001184900.3(CARD8):c.28A>C (p.Ser10Arg) rs2044921320
NM_001184900.3(CARD8):c.290C>T (p.Ala97Val)
NM_001184900.3(CARD8):c.2T>C (p.Met1Thr) rs2146672566
NM_001184900.3(CARD8):c.302T>G (p.Leu101Trp) rs183473284
NM_001184900.3(CARD8):c.308G>T (p.Arg103Leu) rs536343060
NM_001184900.3(CARD8):c.334G>C (p.Gly112Arg)
NM_001184900.3(CARD8):c.334G>T (p.Gly112Trp)
NM_001184900.3(CARD8):c.340dup (p.Asp114fs)
NM_001184900.3(CARD8):c.34A>G (p.Ser12Gly)
NM_001184900.3(CARD8):c.350+1G>A
NM_001184900.3(CARD8):c.368A>G (p.Glu123Gly)
NM_001184900.3(CARD8):c.379G>C (p.Gly127Arg)
NM_001184900.3(CARD8):c.383A>G (p.Gln128Arg)
NM_001184900.3(CARD8):c.388dup (p.Ser130fs)
NM_001184900.3(CARD8):c.391+1G>C
NM_001184900.3(CARD8):c.391+5T>C rs937431054
NM_001184900.3(CARD8):c.391G>A (p.Gly131Arg)
NM_001184900.3(CARD8):c.392G>A (p.Gly131Glu)
NM_001184900.3(CARD8):c.403T>C (p.Ser135Pro)
NM_001184900.3(CARD8):c.40del (p.Glu14fs)
NM_001184900.3(CARD8):c.412A>T (p.Asn138Tyr)
NM_001184900.3(CARD8):c.414T>A (p.Asn138Lys) rs2146253244
NM_001184900.3(CARD8):c.415C>T (p.Gln139Ter)
NM_001184900.3(CARD8):c.434C>A (p.Ala145Asp)
NM_001184900.3(CARD8):c.439A>G (p.Lys147Glu)
NM_001184900.3(CARD8):c.447T>A (p.Cys149Ter)
NM_001184900.3(CARD8):c.448T>C (p.Phe150Leu)
NM_001184900.3(CARD8):c.456C>G (p.Ile152Met)
NM_001184900.3(CARD8):c.466del (p.Tyr156fs)
NM_001184900.3(CARD8):c.473A>G (p.Asn158Ser)
NM_001184900.3(CARD8):c.476G>A (p.Arg159His)
NM_001184900.3(CARD8):c.479A>G (p.Gln160Arg)
NM_001184900.3(CARD8):c.485T>C (p.Leu162Pro)
NM_001184900.3(CARD8):c.497G>C (p.Gly166Ala) rs751018827
NM_001184900.3(CARD8):c.505G>A (p.Asp169Asn)
NM_001184900.3(CARD8):c.509T>C (p.Val170Ala) rs74990657
NM_001184900.3(CARD8):c.523A>G (p.Lys175Glu)
NM_001184900.3(CARD8):c.534C>A (p.Asn178Lys)
NM_001184900.3(CARD8):c.537A>G (p.Arg179=)
NM_001184900.3(CARD8):c.542+3A>C
NM_001184900.3(CARD8):c.542G>A (p.Ser181Asn) rs2146245109
NM_001184900.3(CARD8):c.543-12G>A rs1401972052
NM_001184900.3(CARD8):c.543C>T (p.Ser181=)
NM_001184900.3(CARD8):c.544G>A (p.Val182Ile)
NM_001184900.3(CARD8):c.549G>T (p.Trp183Cys)
NM_001184900.3(CARD8):c.559G>A (p.Ala187Thr)
NM_001184900.3(CARD8):c.574_575del (p.Trp192fs)
NM_001184900.3(CARD8):c.581C>T (p.Ala194Val)
NM_001184900.3(CARD8):c.590T>C (p.Leu197Pro)
NM_001184900.3(CARD8):c.595T>C (p.Phe199Leu)
NM_001184900.3(CARD8):c.59G>A (p.Arg20Gln)
NM_001184900.3(CARD8):c.625A>G (p.Ile209Val)
NM_001184900.3(CARD8):c.630G>T (p.Ala210=)
NM_001184900.3(CARD8):c.658C>G (p.Leu220Val)
NM_001184900.3(CARD8):c.668A>G (p.Gln223Arg)
NM_001184900.3(CARD8):c.676G>C (p.Glu226Gln) rs2042740669
NM_001184900.3(CARD8):c.679C>G (p.Gln227Glu) rs2042739230
NM_001184900.3(CARD8):c.680A>G (p.Gln227Arg)
NM_001184900.3(CARD8):c.682T>C (p.Trp228Arg)
NM_001184900.3(CARD8):c.688G>A (p.Val230Met)
NM_001184900.3(CARD8):c.704T>C (p.Phe235Ser)
NM_001184900.3(CARD8):c.706G>T (p.Asp236Tyr)
NM_001184900.3(CARD8):c.713C>G (p.Thr238Ser)
NM_001184900.3(CARD8):c.727G>A (p.Glu243Lys)
NM_001184900.3(CARD8):c.737C>T (p.Ala246Val)
NM_001184900.3(CARD8):c.739G>A (p.Glu247Lys)
NM_001184900.3(CARD8):c.743T>G (p.Ile248Ser)
NM_001184900.3(CARD8):c.746del (p.His249fs)
NM_001184900.3(CARD8):c.748C>T (p.Leu250Phe)
NM_001184900.3(CARD8):c.754C>A (p.His252Asn) rs764067338
NM_001184900.3(CARD8):c.754C>G (p.His252Asp) rs764067338
NM_001184900.3(CARD8):c.754C>T (p.His252Tyr) rs764067338
NM_001184900.3(CARD8):c.762C>G (p.Ile254Met)
NM_001184900.3(CARD8):c.767_768delinsCT (p.Leu256Pro) rs2146201858
NM_001184900.3(CARD8):c.770A>G (p.Gln257Arg)
NM_001184900.3(CARD8):c.772+5T>C
NM_001184900.3(CARD8):c.773-3C>T
NM_001184900.3(CARD8):c.773-4_773-3insGGAGGCTGTGGGGGCCGCTGGGGTGCGTGCCGTCTCACTGCTGTTGTGGTTCTCCTGGTGGCTGGGGACAGCAGCAGGGCCTAGGAAGGATGCACGCTCTTTCGCCTCTGCATCTTTGGAGTTCGATACTTTTCTGACCTGGACTTTCCTCACCAGCAGAAAGTGTCTTCTGCTATTTCGGACCAGTAGAAATGTAGGTGCATT
NM_001184900.3(CARD8):c.787G>A (p.Val263Ile)
NM_001184900.3(CARD8):c.797T>G (p.Phe266Cys)
NM_001184900.3(CARD8):c.802G>A (p.Val268Ile) rs201339858
NM_001184900.3(CARD8):c.802G>T (p.Val268Phe)
NM_001184900.3(CARD8):c.847C>T (p.Arg283Trp)
NM_001184900.3(CARD8):c.848G>A (p.Arg283Gln)
NM_001184900.3(CARD8):c.850G>T (p.Val284Leu)
NM_001184900.3(CARD8):c.851T>A (p.Val284Glu)
NM_001184900.3(CARD8):c.853G>T (p.Glu285Ter) rs2146193028
NM_001184900.3(CARD8):c.856C>A (p.Pro286Thr) rs2146192734
NM_001184900.3(CARD8):c.863A>C (p.Tyr288Ser)
NM_001184900.3(CARD8):c.869T>C (p.Val290Ala)
NM_001184900.3(CARD8):c.878G>A (p.Ser293Asn)
NM_001184900.3(CARD8):c.878G>T (p.Ser293Ile)
NM_001184900.3(CARD8):c.897G>A (p.Met299Ile) rs2146190684
NM_001184900.3(CARD8):c.899G>T (p.Gly300Val)
NM_001184900.3(CARD8):c.8A>G (p.Lys3Arg)
NM_001184900.3(CARD8):c.911G>A (p.Arg304Gln)
NM_001184900.3(CARD8):c.913A>T (p.Ile305Phe)
NM_001184900.3(CARD8):c.915C>G (p.Ile305Met)
NM_001184900.3(CARD8):c.928C>T (p.Arg310Cys)
NM_001184900.3(CARD8):c.953A>G (p.Asn318Ser) rs2146186919
NM_001184900.3(CARD8):c.963del (p.Tyr322fs)
NM_001184900.3(CARD8):c.974C>T (p.Pro325Leu)
NM_001184900.3(CARD8):c.982G>A (p.Glu328Lys)
NM_001184900.3(CARD8):c.986A>T (p.Asp329Val)
NM_001184900.3(CARD8):c.989T>C (p.Ile330Thr)
NM_001184900.3(CARD8):c.998A>G (p.His333Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.