ClinVar Miner

List of variants in gene DCX reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001195553.2(DCX):c.-22-312_-22-306del rs200417598 0.07837
NM_001195553.2(DCX):c.808+284C>G rs17222328 0.05268
NM_001195553.2(DCX):c.705+29G>A rs61036541 0.01792
NM_001195553.2(DCX):c.1044+132G>C rs10482456 0.01551
NM_001195553.2(DCX):c.947-46T>C rs113181679 0.01340
NM_001195553.2(DCX):c.705+48A>G rs201805884 0.00836
NM_001195553.2(DCX):c.705+95C>T rs146900657 0.00535
NM_001195553.2(DCX):c.*273C>T rs111957035 0.00508
NM_001195553.2(DCX):c.808+224C>T rs144344521 0.00388
NM_001195553.2(DCX):c.946+275C>G rs188874241 0.00387
NM_001195553.2(DCX):c.588T>C (p.Arg196=) rs138706968 0.00376
NM_001195553.2(DCX):c.809-9T>C rs199537326 0.00073
NM_001195553.2(DCX):c.96C>T (p.Ser32=) rs148472336 0.00060
NM_001195553.2(DCX):c.666C>T (p.Thr222=) rs143501582 0.00032
NM_001195553.2(DCX):c.587G>A (p.Arg196His) rs56030372 0.00001
NM_001195553.2(DCX):c.892C>T (p.Pro298Ser) rs780994284 0.00001
NM_001195553.2(DCX):c.-22-336T>G
NM_001195553.2(DCX):c.1031G>C (p.Arg344Pro) rs375993711
NM_001195553.2(DCX):c.103T>C (p.Cys35Arg)
NM_001195553.2(DCX):c.1044+234G>A rs41311727
NM_001195553.2(DCX):c.1087G>C (p.Gly363Arg) rs1064795284
NM_001195553.2(DCX):c.192C>G (p.Tyr64Ter) rs764964209
NM_001195553.2(DCX):c.211G>A (p.Ala71Thr) rs104894786
NM_001195553.2(DCX):c.233G>T (p.Arg78Leu) rs104894784
NM_001195553.2(DCX):c.263C>T (p.Thr88Met)
NM_001195553.2(DCX):c.274_277del (p.Ser92fs) rs1556405065
NM_001195553.2(DCX):c.304C>G (p.Arg102Gly) rs587783541
NM_001195553.2(DCX):c.30_31del (p.Arg11_Asp12insTer) rs1085307851
NM_001195553.2(DCX):c.320T>C (p.Ile107Thr) rs1064795584
NM_001195553.2(DCX):c.364+1del rs1064793735
NM_001195553.2(DCX):c.389A>G (p.Asp130Gly) rs1064795427
NM_001195553.2(DCX):c.421A>G (p.Asn141Asp) rs2147263279
NM_001195553.2(DCX):c.467dup (p.Met156fs) rs886041736
NM_001195553.2(DCX):c.478dup (p.Gln160fs) rs2147263208
NM_001195553.2(DCX):c.505C>T (p.Gln169Ter) rs1064794223
NM_001195553.2(DCX):c.532C>T (p.Arg178Cys) rs587783558
NM_001195553.2(DCX):c.556C>T (p.Arg186Cys) rs587783562
NM_001195553.2(DCX):c.557G>A (p.Arg186His) rs587783563
NM_001195553.2(DCX):c.557G>T (p.Arg186Leu) rs587783563
NM_001195553.2(DCX):c.572C>G (p.Pro191Arg) rs587783566
NM_001195553.2(DCX):c.574C>T (p.Arg192Trp) rs104894780
NM_001195553.2(DCX):c.586C>T (p.Arg196Cys) rs587783568
NM_001195553.2(DCX):c.596T>C (p.Leu199Pro) rs587783569
NM_001195553.2(DCX):c.596T>G (p.Leu199Arg)
NM_001195553.2(DCX):c.64C>T (p.Arg22Trp)
NM_001195553.2(DCX):c.65G>A (p.Arg22Gln)
NM_001195553.2(DCX):c.667G>C (p.Gly223Arg) rs587783577
NM_001195553.2(DCX):c.684_685del (p.Tyr229fs) rs1556401744
NM_001195553.2(DCX):c.703C>T (p.Gln235Ter)
NM_001195553.2(DCX):c.705+1G>A rs2147262624
NM_001195553.2(DCX):c.706-2A>G rs886039339
NM_001195553.2(DCX):c.752C>A (p.Ala251Asp) rs1085307919
NM_001195553.2(DCX):c.757G>C (p.Gly253Arg) rs1556376311
NM_001195553.2(DCX):c.772C>T (p.Arg258Cys) rs727503897
NM_001195553.2(DCX):c.777T>A (p.Tyr259Ter) rs747557639
NM_001195553.2(DCX):c.800A>G (p.Asp267Gly)
NM_001195553.2(DCX):c.814C>T (p.Arg272Ter) rs587783590
NM_001195553.2(DCX):c.874A>G (p.Lys292Glu)
NM_001195553.2(DCX):c.890G>C (p.Ser297Thr)
NM_001195553.2(DCX):c.907C>T (p.Arg303Ter) rs587783592
NM_001195553.2(DCX):c.955A>G (p.Thr319Ala) rs2147595104

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