ClinVar Miner

List of variants in gene KCNT1 reported as likely benign for Seizures

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Total variants: 55
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HGVS dbSNP
NM_020822.3(KCNT1):c.1008C>T (p.Cys336=) rs540422455
NM_020822.3(KCNT1):c.1134C>T (p.Val378=) rs149960236
NM_020822.3(KCNT1):c.1182C>T (p.Tyr394=) rs372491855
NM_020822.3(KCNT1):c.1258C>T (p.Leu420=) rs199996353
NM_020822.3(KCNT1):c.1394C>T (p.Thr465Met) rs539139475
NM_020822.3(KCNT1):c.1422C>T (p.Arg474=) rs372250372
NM_020822.3(KCNT1):c.1443C>T (p.Phe481=) rs576446992
NM_020822.3(KCNT1):c.1533G>A (p.Glu511=) rs151080601
NM_020822.3(KCNT1):c.1545C>T (p.Ala515=)
NM_020822.3(KCNT1):c.1626A>G (p.Gly542=) rs537431085
NM_020822.3(KCNT1):c.1628A>G (p.Gln543Arg) rs200173000
NM_020822.3(KCNT1):c.1726G>A (p.Glu576Lys) rs147306623
NM_020822.3(KCNT1):c.1928G>A (p.Arg643Gln) rs141281093
NM_020822.3(KCNT1):c.2034C>T (p.Gly678=) rs369983077
NM_020822.3(KCNT1):c.2051C>T (p.Thr684Met) rs377506738
NM_020822.3(KCNT1):c.2052G>A (p.Thr684=) rs376314779
NM_020822.3(KCNT1):c.2070C>T (p.Gly690=) rs370155559
NM_020822.3(KCNT1):c.2142G>A (p.Leu714=) rs370580872
NM_020822.3(KCNT1):c.2211G>A (p.Thr737=)
NM_020822.3(KCNT1):c.2220C>G (p.Asp740Glu) rs148162797
NM_020822.3(KCNT1):c.2223C>T (p.Asp741=) rs144118960
NM_020822.3(KCNT1):c.2236G>A (p.Val746Met) rs559344618
NM_020822.3(KCNT1):c.2376C>T (p.Asp792=) rs149028586
NM_020822.3(KCNT1):c.2543A>G (p.Glu848Gly) rs149804567
NM_020822.3(KCNT1):c.2589G>A (p.Val863=)
NM_020822.3(KCNT1):c.2729G>A (p.Arg910Gln) rs151272083
NM_020822.3(KCNT1):c.2892C>T (p.Phe964=) rs146904895
NM_020822.3(KCNT1):c.2994G>A (p.Leu998=) rs143198263
NM_020822.3(KCNT1):c.2997C>T (p.Asp999=) rs771951768
NM_020822.3(KCNT1):c.3001A>G (p.Thr1001Ala) rs143780942
NM_020822.3(KCNT1):c.309G>T (p.Leu103=) rs767894239
NM_020822.3(KCNT1):c.3162C>T (p.His1054=) rs146272510
NM_020822.3(KCNT1):c.3239G>T (p.Gly1080Val) rs200250181
NM_020822.3(KCNT1):c.3256G>A (p.Gly1086Arg) rs201156458
NM_020822.3(KCNT1):c.3317G>A (p.Arg1106Gln) rs561255614
NM_020822.3(KCNT1):c.3320G>A (p.Arg1107His)
NM_020822.3(KCNT1):c.333G>A (p.Ser111=) rs56008253
NM_020822.3(KCNT1):c.3383C>T (p.Ala1128Val) rs143704418
NM_020822.3(KCNT1):c.3558C>T (p.Pro1186=) rs148525032
NM_020822.3(KCNT1):c.3606C>T (p.Asp1202=) rs140628824
NM_020822.3(KCNT1):c.3632C>G (p.Ser1211Cys) rs752729337
NM_020822.3(KCNT1):c.3641G>A (p.Arg1214Gln) rs138282349
NM_020822.3(KCNT1):c.3668C>T (p.Ser1223Leu)
NM_020822.3(KCNT1):c.3681C>T (p.Pro1227=) rs149049198
NM_020822.3(KCNT1):c.3685A>G (p.Thr1229Ala) rs74533482
NM_020822.3(KCNT1):c.3690C>T (p.Arg1230=) rs141521745
NM_020822.3(KCNT1):c.474G>A (p.Ser158=) rs139076605
NM_020822.3(KCNT1):c.522G>A (p.Met174Ile) rs147551342
NM_020822.3(KCNT1):c.585C>T (p.Ile195=)
NM_020822.3(KCNT1):c.625C>T (p.Arg209Cys)
NM_020822.3(KCNT1):c.762T>C (p.Asn254=) rs1481356544
NM_020822.3(KCNT1):c.861C>T (p.Cys287=)
NM_020822.3(KCNT1):c.885G>A (p.Ala295=) rs142756900
NM_020822.3(KCNT1):c.985C>T (p.Leu329=) rs147165522
NM_020822.3(KCNT1):c.99A>G (p.Gln33=) rs146152956

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