ClinVar Miner

List of variants in gene KCNT1 reported as benign by Invitae

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Total variants: 47
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HGVS dbSNP
NM_020822.3(KCNT1):c.1008C>T (p.Cys336=) rs540422455
NM_020822.3(KCNT1):c.1056C>G (p.Leu352=) rs116691849
NM_020822.3(KCNT1):c.1104G>A (p.Ala368=) rs146032445
NM_020822.3(KCNT1):c.1134C>T (p.Val378=) rs149960236
NM_020822.3(KCNT1):c.116C>T (p.Pro39Leu) rs201051863
NM_020822.3(KCNT1):c.1182C>T (p.Tyr394=) rs372491855
NM_020822.3(KCNT1):c.1533G>A (p.Glu511=) rs151080601
NM_020822.3(KCNT1):c.1614C>T (p.Arg538=) rs368876173
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.1776C>T (p.Gly592=) rs769406687
NM_020822.3(KCNT1):c.1879A>G (p.Ile627Val) rs143355299
NM_020822.3(KCNT1):c.2008+10G>C rs752453368
NM_020822.3(KCNT1):c.2142G>A (p.Leu714=) rs370580872
NM_020822.3(KCNT1):c.2210C>T (p.Thr737Met) rs61744696
NM_020822.3(KCNT1):c.2235C>T (p.Ser745=) rs146810749
NM_020822.3(KCNT1):c.2349+7C>T rs190849453
NM_020822.3(KCNT1):c.2376C>T (p.Asp792=) rs149028586
NM_020822.3(KCNT1):c.2430C>T (p.Ala810=) rs139114208
NM_020822.3(KCNT1):c.2619C>T (p.Gly873=) rs144659358
NM_020822.3(KCNT1):c.2691G>A (p.Ala897=) rs142642528
NM_020822.3(KCNT1):c.2729+9A>G rs12005420
NM_020822.3(KCNT1):c.2841+10C>T rs765179799
NM_020822.3(KCNT1):c.2892C>T (p.Phe964=) rs146904895
NM_020822.3(KCNT1):c.2943+6C>T rs28612938
NM_020822.3(KCNT1):c.2994G>A (p.Leu998=) rs143198263
NM_020822.3(KCNT1):c.3006G>A (p.Pro1002=) rs377162900
NM_020822.3(KCNT1):c.3039C>T (p.Thr1013=) rs148001061
NM_020822.3(KCNT1):c.30G>A (p.Pro10=) rs139034501
NM_020822.3(KCNT1):c.3157-8C>T rs371874401
NM_020822.3(KCNT1):c.3295C>T (p.Pro1099Ser) rs200642629
NM_020822.3(KCNT1):c.3312G>A (p.Leu1104=) rs149416418
NM_020822.3(KCNT1):c.333G>A (p.Ser111=) rs56008253
NM_020822.3(KCNT1):c.3388G>A (p.Ala1130Thr) rs138421850
NM_020822.3(KCNT1):c.3390G>A (p.Ala1130=) rs77912754
NM_020822.3(KCNT1):c.3495C>T (p.Thr1165=) rs374429090
NM_020822.3(KCNT1):c.3555G>T (p.Pro1185=) rs144068763
NM_020822.3(KCNT1):c.3606C>T (p.Asp1202=) rs140628824
NM_020822.3(KCNT1):c.3681C>T (p.Pro1227=) rs149049198
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.59G>C (p.Gly20Ala) rs146292575
NM_020822.3(KCNT1):c.711C>G (p.Pro237=) rs117286274
NM_020822.3(KCNT1):c.885G>A (p.Ala295=) rs142756900
NM_020822.3(KCNT1):c.978A>G (p.Pro326=) rs61739517
NM_020822.3(KCNT1):c.985C>T (p.Leu329=) rs147165522
NM_020822.3(KCNT1):c.99A>G (p.Gln33=) rs146152956

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