ClinVar Miner

List of variants in gene KCNC1 reported as uncertain significance for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_001112741.1(KCNC1):c.1065C>T (p.Gly355=)
NM_001112741.1(KCNC1):c.1154A>C (p.Lys385Thr) rs1554991360
NM_001112741.1(KCNC1):c.121G>A (p.Asp41Asn) rs1192156090
NM_001112741.1(KCNC1):c.1261G>A (p.Ala421Thr) rs1565162836
NM_001112741.1(KCNC1):c.1262C>T (p.Ala421Val) rs1554991378
NM_001112741.1(KCNC1):c.1269G>A (p.Ala423=)
NM_001112741.1(KCNC1):c.131G>A (p.Ser44Asn)
NM_001112741.1(KCNC1):c.1399G>C (p.Gly467Arg)
NM_001112741.1(KCNC1):c.1421C>A (p.Ser474Tyr) rs1554991422
NM_001112741.1(KCNC1):c.1426G>A (p.Val476Ile) rs146311746
NM_001112741.1(KCNC1):c.1438C>A (p.His480Asn) rs1554991425
NM_001112741.1(KCNC1):c.1450C>G (p.Gln484Glu) rs376505218
NM_001112741.1(KCNC1):c.1505A>G (p.Asp502Gly)
NM_001112741.1(KCNC1):c.1574C>T (p.Ala525Val) rs1169785679
NM_001112741.1(KCNC1):c.1619G>A (p.Arg540His)
NM_001112741.1(KCNC1):c.1625G>A (p.Arg542Lys)
NM_001112741.1(KCNC1):c.1627T>C (p.Tyr543His) rs775725087
NM_001112741.1(KCNC1):c.1630G>A (p.Gly544Arg) rs758088373
NM_001112741.1(KCNC1):c.1654G>A (p.Gly552Arg)
NM_001112741.1(KCNC1):c.1659G>T (p.Glu553Asp) rs372580647
NM_001112741.1(KCNC1):c.1673C>G (p.Pro558Arg)
NM_001112741.1(KCNC1):c.1681G>A (p.Gly561Arg)
NM_001112741.1(KCNC1):c.1739A>G (p.Glu580Gly) rs1284857169
NM_001112741.1(KCNC1):c.223A>G (p.Lys75Glu) rs1565152713
NM_001112741.1(KCNC1):c.394G>A (p.Asp132Asn)
NM_001112741.1(KCNC1):c.421G>T (p.Asp141Tyr)
NM_001112741.1(KCNC1):c.433G>C (p.Gly145Arg) rs759773311
NM_001112741.1(KCNC1):c.435C>T (p.Gly145=)
NM_001112741.1(KCNC1):c.494C>T (p.Pro165Leu) rs749790557
NM_001112741.1(KCNC1):c.499G>T (p.Gly167Cys) rs1274575581
NM_001112741.1(KCNC1):c.523C>T (p.Arg175Cys)
NM_001112741.1(KCNC1):c.554C>T (p.Ser185Leu) rs1565152898
NM_001112741.1(KCNC1):c.611T>C (p.Ile204Thr) rs1554991304
NM_001112741.1(KCNC1):c.654C>A (p.Ile218=) rs747207268
NM_001112741.1(KCNC1):c.677A>T (p.Asn226Ile)
NM_001112741.1(KCNC1):c.692C>T (p.Thr231Met) rs1554991314
NM_001112741.1(KCNC1):c.696A>C (p.Gln232His) rs775885483
NM_001112741.1(KCNC1):c.701G>A (p.Arg234His) rs763794003
NM_001112741.1(KCNC1):c.709C>T (p.Arg237Trp)
NM_001112741.1(KCNC1):c.788G>A (p.Arg263His)

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