ClinVar Miner

List of variants in gene KCNC1 reported as likely benign for Epilepsy, progressive myoclonic 7

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Total variants: 20
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HGVS dbSNP
NM_001112741.1(KCNC1):c.1505-8G>A rs1353872876
NM_001112741.1(KCNC1):c.1518T>C (p.Asn506=) rs747283873
NM_001112741.1(KCNC1):c.1584C>G (p.Pro528=) rs1044982783
NM_001112741.1(KCNC1):c.1653C>T (p.Thr551=) rs368328020
NM_001112741.1(KCNC1):c.1662C>T (p.Tyr554=) rs578025939
NM_001112741.1(KCNC1):c.51G>A (p.Thr17=) rs1423569470
NM_001112741.1(KCNC1):c.594C>T (p.Phe198=) rs371344625
NM_001112741.1(KCNC1):c.636C>T (p.His212=) rs745968113
NM_001112741.1(KCNC1):c.677A>T (p.Asn226Ile) rs73424032
NM_001112741.1(KCNC1):c.683G>T (p.Arg228Leu) rs200873319
NM_001112741.1(KCNC1):c.831G>T (p.Ser277=) rs765494674
NM_001112741.1(KCNC1):c.96G>A (p.Thr32=) rs140637569
NM_001112741.2(KCNC1):c.102C>A (p.Leu34=) rs370742331
NM_001112741.2(KCNC1):c.1119C>T (p.Pro373=) rs143960025
NM_001112741.2(KCNC1):c.120C>G (p.Pro40=) rs1590088845
NM_001112741.2(KCNC1):c.1263G>A (p.Ala421=) rs915600389
NM_001112741.2(KCNC1):c.327C>T (p.Tyr109=) rs1590088932
NM_001112741.2(KCNC1):c.402G>A (p.Ala134=) rs1590089002
NM_001112741.2(KCNC1):c.912G>A (p.Lys304=) rs114815696
NM_001112741.2(KCNC1):c.915C>T (p.Asp305=) rs757117157

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