ClinVar Miner

List of variants in gene DCX reported as pathogenic for not provided

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001195553.2(DCX):c.587G>A (p.Arg196His) rs56030372 0.00001
NC_000023.10:g.(?_110576259)_(110576401_?)del
NM_001195553.2(DCX):c.115C>T (p.Arg39Ter) rs587783519
NM_001195553.2(DCX):c.176G>A (p.Arg59His) rs122457137
NM_001195553.2(DCX):c.190T>G (p.Tyr64Asp)
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.232C>T (p.Arg78Cys) rs587783535
NM_001195553.2(DCX):c.233G>T (p.Arg78Leu) rs104894784
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.364+1del rs1064793735
NM_001195553.2(DCX):c.365-1G>T rs2147263424
NM_001195553.2(DCX):c.37_38del (p.Lys13fs) rs2147276732
NM_001195553.2(DCX):c.409G>T (p.Glu137Ter) rs587783550
NM_001195553.2(DCX):c.414_415insG (p.Thr139fs) rs2147263289
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.538A>G (p.Lys180Glu) rs587783560
NM_001195553.2(DCX):c.540G>T (p.Lys180Asn) rs1927758267
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.667G>A (p.Gly223Arg) rs587783577
NM_001195553.2(DCX):c.681dup (p.Leu228fs) rs587783579
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.751G>T (p.Ala251Ser) rs587783585
NM_001195553.2(DCX):c.763G>T (p.Glu255Ter) rs727503898
NM_001195553.2(DCX):c.777T>A (p.Tyr259Ter) rs747557639
NM_001195553.2(DCX):c.781C>T (p.Gln261Ter) rs587783588
NM_001195553.2(DCX):c.814C>T (p.Arg272Ter) rs587783590
NM_001195553.2(DCX):c.907C>T (p.Arg303Ter) rs587783592

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