ClinVar Miner

List of variants in gene KCNT1 reported as likely benign by Invitae

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Gene type:
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Total variants: 99
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HGVS dbSNP
NM_020822.3(KCNT1):c.1038C>T (p.Phe346=) rs767434859
NM_020822.3(KCNT1):c.1119C>T (p.His373=) rs1052932341
NM_020822.3(KCNT1):c.1258C>T (p.Leu420=) rs199996353
NM_020822.3(KCNT1):c.1284G>A (p.Arg428=) rs943112493
NM_020822.3(KCNT1):c.130G>T (p.Gly44Cys) rs773228285
NM_020822.3(KCNT1):c.1326_1327delinsAT (p.Met443Leu) rs1554773537
NM_020822.3(KCNT1):c.1337+7G>A rs374975940
NM_020822.3(KCNT1):c.1365C>T (p.Ile455=) rs1305510057
NM_020822.3(KCNT1):c.1380C>T (p.Asn460=) rs566700584
NM_020822.3(KCNT1):c.1422C>T (p.Arg474=) rs372250372
NM_020822.3(KCNT1):c.1431C>T (p.Ala477=) rs375534850
NM_020822.3(KCNT1):c.1443C>T (p.Phe481=) rs576446992
NM_020822.3(KCNT1):c.1511-4G>A rs368480443
NM_020822.3(KCNT1):c.1638G>A (p.Pro546=) rs138352399
NM_020822.3(KCNT1):c.1725C>T (p.Tyr575=) rs373520472
NM_020822.3(KCNT1):c.1769+8C>T rs371287985
NM_020822.3(KCNT1):c.1769+9G>A rs758402819
NM_020822.3(KCNT1):c.1788C>T (p.Ile596=) rs373444768
NM_020822.3(KCNT1):c.1803G>A (p.Glu601=) rs376892911
NM_020822.3(KCNT1):c.1806C>T (p.Asp602=) rs1060505001
NM_020822.3(KCNT1):c.1824G>A (p.Leu608=) rs764141661
NM_020822.3(KCNT1):c.1881C>T (p.Ile627=) rs1554775088
NM_020822.3(KCNT1):c.1899G>A (p.Ser633=) rs371135108
NM_020822.3(KCNT1):c.1946C>T (p.Ser649Leu) rs747671066
NM_020822.3(KCNT1):c.1947G>A (p.Ser649=) rs779903423
NM_020822.3(KCNT1):c.1963G>C (p.Glu655Gln) rs770039542
NM_020822.3(KCNT1):c.1983C>T (p.Pro661=) rs533528985
NM_020822.3(KCNT1):c.2008+7C>T rs372707698
NM_020822.3(KCNT1):c.2008+8G>A rs759334176
NM_020822.3(KCNT1):c.2030A>G (p.Gln677Arg) rs1060505000
NM_020822.3(KCNT1):c.2034C>T (p.Gly678=) rs369983077
NM_020822.3(KCNT1):c.2049T>C (p.Pro683=) rs1234688449
NM_020822.3(KCNT1):c.2051C>T (p.Thr684Met) rs377506738
NM_020822.3(KCNT1):c.2058C>T (p.Ser686=) rs111647144
NM_020822.3(KCNT1):c.2070C>T (p.Gly690=) rs370155559
NM_020822.3(KCNT1):c.2136C>T (p.Pro712=) rs377516058
NM_020822.3(KCNT1):c.2175C>T (p.Cys725=) rs368450848
NM_020822.3(KCNT1):c.2214G>A (p.Pro738=) rs142424896
NM_020822.3(KCNT1):c.2220C>G (p.Asp740Glu) rs148162797
NM_020822.3(KCNT1):c.2222A>G (p.Asp741Gly) rs756359375
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.2295C>T (p.Thr765=) rs765278495
NM_020822.3(KCNT1):c.231C>T (p.Asp77=) rs370998066
NM_020822.3(KCNT1):c.2321C>T (p.Ala774Val) rs777479133
NM_020822.3(KCNT1):c.2337G>A (p.Leu779=) rs544099606
NM_020822.3(KCNT1):c.2350-10C>T rs367855961
NM_020822.3(KCNT1):c.2451C>T (p.Phe817=) rs942926305
NM_020822.3(KCNT1):c.2454C>T (p.Ile818=) rs149452823
NM_020822.3(KCNT1):c.2543A>G (p.Glu848Gly) rs149804567
NM_020822.3(KCNT1):c.2568C>T (p.Val856=) rs1554777911
NM_020822.3(KCNT1):c.2594+7C>T rs545094921
NM_020822.3(KCNT1):c.2670C>T (p.Ser890=) rs765403435
NM_020822.3(KCNT1):c.2729G>A (p.Arg910Gln) rs151272083
NM_020822.3(KCNT1):c.279C>T (p.Asn93=) rs183022730
NM_020822.3(KCNT1):c.2847G>A (p.Glu949=) rs779429071
NM_020822.3(KCNT1):c.2856T>C (p.Asn952=) rs147671362
NM_020822.3(KCNT1):c.2895C>T (p.Ala965=) rs776550763
NM_020822.3(KCNT1):c.2898C>T (p.Ala966=) rs762968242
NM_020822.3(KCNT1):c.2916C>T (p.Ile972=) rs878855056
NM_020822.3(KCNT1):c.2949C>T (p.Phe983=) rs764574987
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.3003G>A (p.Thr1001=) rs560435329
NM_020822.3(KCNT1):c.3015G>T (p.Gly1005=) rs368875875
NM_020822.3(KCNT1):c.3036C>T (p.Ile1012=) rs201120894
NM_020822.3(KCNT1):c.3048C>T (p.Asp1016=) rs748942066
NM_020822.3(KCNT1):c.3063G>A (p.Thr1021=) rs760974671
NM_020822.3(KCNT1):c.309G>T (p.Leu103=) rs767894239
NM_020822.3(KCNT1):c.3138C>T (p.His1046=) rs138533589
NM_020822.3(KCNT1):c.3147C>T (p.Ser1049=) rs765432746
NM_020822.3(KCNT1):c.3153G>A (p.Ser1051=) rs141802876
NM_020822.3(KCNT1):c.3239G>T (p.Gly1080Val) rs200250181
NM_020822.3(KCNT1):c.3246C>T (p.Arg1082=) rs765774534
NM_020822.3(KCNT1):c.3256G>A (p.Gly1086Arg) rs201156458
NM_020822.3(KCNT1):c.3274C>T (p.Arg1092Cys) rs1060503695
NM_020822.3(KCNT1):c.3297C>G (p.Pro1099=) rs759060691
NM_020822.3(KCNT1):c.3317G>A (p.Arg1106Gln) rs561255614
NM_020822.3(KCNT1):c.3340C>T (p.Arg1114Trp) rs370085077
NM_020822.3(KCNT1):c.3383C>T (p.Ala1128Val) rs143704418
NM_020822.3(KCNT1):c.3387C>T (p.Ala1129=) rs372410150
NM_020822.3(KCNT1):c.3437G>A (p.Arg1146His) rs368339692
NM_020822.3(KCNT1):c.3461A>G (p.Lys1154Arg) rs779810960
NM_020822.3(KCNT1):c.3501C>T (p.Tyr1167=) rs773575309
NM_020822.3(KCNT1):c.3502G>A (p.Asp1168Asn) rs747317425
NM_020822.3(KCNT1):c.3618C>T (p.His1206=) rs577378740
NM_020822.3(KCNT1):c.3641G>A (p.Arg1214Gln) rs138282349
NM_020822.3(KCNT1):c.3664C>T (p.Leu1222=) rs755694160
NM_020822.3(KCNT1):c.3685A>G (p.Thr1229Ala) rs74533482
NM_020822.3(KCNT1):c.408C>T (p.Leu136=) rs370046449
NM_020822.3(KCNT1):c.522G>A (p.Met174Ile) rs147551342
NM_020822.3(KCNT1):c.541-7C>A rs1489319809
NM_020822.3(KCNT1):c.760-9C>T rs1554771446
NM_020822.3(KCNT1):c.921C>T (p.Phe307=) rs878855057
NM_020822.3(KCNT1):c.942C>T (p.Thr314=) rs144766991
NM_020822.3(KCNT1):c.94G>T (p.Gly32Cys) rs754823810
NM_020822.3(KCNT1):c.951C>T (p.Tyr317=) rs747685419
NM_020822.3(KCNT1):c.957C>T (p.Asp319=) rs148562086
NM_020822.3(KCNT1):c.981G>A (p.Ser327=) rs373317695

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