ClinVar Miner

List of variants in gene DCX reported as uncertain significance

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001195553.2(DCX):c.-22-491A>G rs1298342663 0.00002
NM_001195553.2(DCX):c.-22-494G>T rs746052967 0.00002
NM_001195553.2(DCX):c.587G>A (p.Arg196His) rs56030372 0.00001
NM_001195553.2(DCX):c.892C>T (p.Pro298Ser) rs780994284 0.00001
GRCh37/hg19 Xq23(chrX:110531355-110561549)x3
GRCh38/hg38 Xq23(chrX:111294396-111417260)x3
NC_000023.10:g.(?_110544915)_(110544991_?)del
NM_001195553.2(DCX):c.-22-336T>G
NM_001195553.2(DCX):c.-22-366C>T
NM_001195553.2(DCX):c.-22-387T>G rs1928648928
NM_001195553.2(DCX):c.-22-521G>A
NM_001195553.2(DCX):c.1016G>A (p.Ser339Asn)
NM_001195553.2(DCX):c.1031G>C (p.Arg344Pro) rs375993711
NM_001195553.2(DCX):c.103T>C (p.Cys35Arg)
NM_001195553.2(DCX):c.1045G>C (p.Asp349His) rs1556364322
NM_001195553.2(DCX):c.1065del (p.Leu356fs)
NM_001195553.2(DCX):c.1068G>A (p.Leu356=)
NM_001195553.2(DCX):c.1087G>C (p.Gly363Arg) rs1064795284
NM_001195553.2(DCX):c.119C>T (p.Thr40Ile) rs2147276605
NM_001195553.2(DCX):c.139A>C (p.Ser47Arg) rs104894783
NM_001195553.2(DCX):c.155C>A (p.Ala52Asp) rs1556405160
NM_001195553.2(DCX):c.158A>G (p.Lys53Arg)
NM_001195553.2(DCX):c.162G>C (p.Lys54Asn) rs1928591160
NM_001195553.2(DCX):c.187C>T (p.Arg63Cys) rs587783529
NM_001195553.2(DCX):c.211G>A (p.Ala71Thr) rs104894786
NM_001195553.2(DCX):c.263C>G (p.Thr88Arg) rs2147276286
NM_001195553.2(DCX):c.263C>T (p.Thr88Met)
NM_001195553.2(DCX):c.305G>A (p.Arg102His) rs267606317
NM_001195553.2(DCX):c.320T>C (p.Ile107Thr) rs1064795584
NM_001195553.2(DCX):c.35A>G (p.Asp12Gly) rs2147276738
NM_001195553.2(DCX):c.364G>A (p.Gly122Arg) rs587783544
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.438G>T (p.Trp146Cys)
NM_001195553.2(DCX):c.439T>C (p.Ser147Pro)
NM_001195553.2(DCX):c.4G>A (p.Glu2Lys)
NM_001195553.2(DCX):c.518A>G (p.Asn173Ser) rs2147263136
NM_001195553.2(DCX):c.530T>G (p.Val177Gly)
NM_001195553.2(DCX):c.534C>T (p.Arg178=) rs1233974245
NM_001195553.2(DCX):c.545T>A (p.Val182Asp)
NM_001195553.2(DCX):c.557G>A (p.Arg186His) rs587783563
NM_001195553.2(DCX):c.562G>A (p.Gly188Arg) rs2147262967
NM_001195553.2(DCX):c.568A>G (p.Lys190Glu) rs398124556
NM_001195553.2(DCX):c.586C>A (p.Arg196Ser) rs587783568
NM_001195553.2(DCX):c.587G>T (p.Arg196Leu) rs56030372
NM_001195553.2(DCX):c.596T>G (p.Leu199Arg)
NM_001195553.2(DCX):c.598A>T (p.Asn200Tyr)
NM_001195553.2(DCX):c.604A>G (p.Lys202Glu)
NM_001195553.2(DCX):c.613C>G (p.His205Asp)
NM_001195553.2(DCX):c.627A>C (p.Gln209His)
NM_001195553.2(DCX):c.64C>T (p.Arg22Trp)
NM_001195553.2(DCX):c.65G>A (p.Arg22Gln)
NM_001195553.2(DCX):c.667G>A (p.Gly223Arg) rs587783577
NM_001195553.2(DCX):c.677A>C (p.Lys226Thr)
NM_001195553.2(DCX):c.680A>C (p.Lys227Thr)
NM_001195553.2(DCX):c.706-2794G>A
NM_001195553.2(DCX):c.766A>G (p.Lys256Glu)
NM_001195553.2(DCX):c.772C>T (p.Arg258Cys) rs727503897
NM_001195553.2(DCX):c.785A>G (p.Asp262Gly) rs398124557
NM_001195553.2(DCX):c.800A>G (p.Asp267Gly)
NM_001195553.2(DCX):c.809-3C>T rs867300590
NM_001195553.2(DCX):c.832C>G (p.Pro278Ala)
NM_001195553.2(DCX):c.847G>A (p.Gly283Ser) rs1556375513
NM_001195553.2(DCX):c.851C>T (p.Pro284Leu)
NM_001195553.2(DCX):c.874A>G (p.Lys292Glu)
NM_001195553.2(DCX):c.890G>C (p.Ser297Thr)
NM_001195553.2(DCX):c.904C>T (p.Arg302Cys)
NM_001195553.2(DCX):c.946+4588G>T rs2147622525
NM_001195553.2(DCX):c.955A>G (p.Thr319Ala) rs2147595104
NM_001195553.2(DCX):c.973T>A (p.Ser325Thr)

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