ClinVar Miner

List of variants in gene DCX studied for Inborn genetic diseases

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001195553.2(DCX):c.588T>C (p.Arg196=) rs138706968 0.00376
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.856G>T (p.Ala286Ser) rs149495971 0.00032
NM_001195553.2(DCX):c.948A>C (p.Ala316=) rs770799939 0.00008
NM_001195553.2(DCX):c.84C>T (p.Ser28=) rs762988798 0.00006
NM_001195553.2(DCX):c.951C>T (p.Asn317=) rs1204976259 0.00005
NM_001195553.2(DCX):c.587G>A (p.Arg196His) rs56030372 0.00001
NM_001195553.2(DCX):c.774C>T (p.Arg258=) rs771696055 0.00001
NM_001195553.2(DCX):c.-22-345_326del
NM_001195553.2(DCX):c.103T>C (p.Cys35Arg)
NM_001195553.2(DCX):c.1077G>A (p.Ser359=)
NM_001195553.2(DCX):c.115C>T (p.Arg39Ter) rs587783519
NM_001195553.2(DCX):c.155C>A (p.Ala52Asp) rs1556405160
NM_001195553.2(DCX):c.158A>G (p.Lys53Arg)
NM_001195553.2(DCX):c.211G>A (p.Ala71Thr) rs104894786
NM_001195553.2(DCX):c.675C>G (p.Val225=)
NM_001195553.2(DCX):c.814C>T (p.Arg272Ter) rs587783590
NM_001195553.2(DCX):c.81T>G (p.Pro27=)
NM_001195553.2(DCX):c.837A>G (p.Ser279=)
NM_001195553.2(DCX):c.851C>T (p.Pro284Leu)
NM_001195553.2(DCX):c.871C>T (p.Gln291Ter)
NM_001195553.2(DCX):c.908G>A (p.Arg303Gln)
NM_001195553.2(DCX):c.936C>T (p.Asn312=)
NM_001195553.2(DCX):c.954A>T (p.Gly318=)

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